geneid | 89866 |
---|---|
ensemblid | ENSG00000120341.19 |
hgncid | 30301 |
symbol | SEC16B |
name | SEC16 homolog B, endoplasmic reticulum export factor |
refseq_nuc | NM_033127.4 |
refseq_prot | NP_149118.2 |
ensembl_nuc | ENST00000308284.11 |
ensembl_prot | ENSP00000308339.6 |
mane_status | MANE Select |
chr | chr1 |
start | 177928788 |
end | 177970058 |
strand | - |
ver | v1.2 |
region | chr1:177928788-177970058 |
region5000 | chr1:177923788-177975058 |
regionname0 | SEC16B_chr1_177928788_177970058 |
regionname5000 | SEC16B_chr1_177923788_177975058 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1060 | 119 | 25 | 26 | 41 | 7 | 20 | 29 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0002 | 0/0 | 1060 | 68 | 15 | 13 | 27 | 4 | 9 | 22 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003 | 0/1 | 1060 | 68 | 15 | 13 | 33 | 1 | 5 | 26 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004 | 0/0 | 1060 | 57 | 3 | 9 | 40 | 0 | 5 | 31 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0005 | 0/0 | 1060 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0006 | 0/0 | 1060 | 11 | 0 | 0 | 10 | 1 | 0 | 9 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0007 | 0/0 | 1060 | 10 | 1 | 5 | 3 | 0 | 1 | 3 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0008 | 1/0 | 1060 | 9 | 2 | 1 | 5 | 0 | 0 | 4 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0009 | 0/0 | 1071 | 7 | 0 | 1 | 6 | 0 | 0 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0010 | 0/0 | 1060 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0011 | 0/0 | 1060 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0012 | 0/0 | 1060 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0013 | 0/0 | 1060 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0014 | 0/0 | 1071 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0015 | 0/0 | 1060 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0016 | 0/0 | 1060 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0017 | 0/0 | 1060 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0018 | 0/0 | 1060 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0019 | 0/0 | 1060 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0020 | 0/0 | 1060 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0021 | 0/0 | 1060 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0022 | 0/0 | 1060 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0023 | 0/0 | 1071 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0024 | 0/0 | 1060 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0025 | 0/0 | 1071 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0026 | 0/0 | 1071 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0027 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0028 | 0/0 | 1060 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0029 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0030 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0031 | 0/0 | 1060 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0032 | 0/0 | 1060 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0033 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0034 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0035 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0036 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0037 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0038 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0039 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3183 | 68 | 15 | 13 | 27 | 4 | 9 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0002 | 0/0 | 3183 | 44 | 1 | 9 | 29 | 0 | 5 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0003 | 0/0 | 3183 | 44 | 1 | 11 | 27 | 0 | 5 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0004 | 0/0 | 3183 | 28 | 1 | 4 | 20 | 0 | 3 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0005 | 0/0 | 3183 | 28 | 3 | 2 | 17 | 0 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0006 | 0/0 | 3183 | 26 | 4 | 12 | 1 | 3 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0007 | 0/0 | 3183 | 17 | 9 | 6 | 1 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0008 | 0/0 | 3183 | 17 | 14 | 1 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0009 | 0/0 | 3183 | 11 | 0 | 0 | 10 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0010 | 0/0 | 3183 | 10 | 0 | 0 | 10 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0011 | 0/0 | 3183 | 8 | 6 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0012 | 1/0 | 3183 | 7 | 1 | 0 | 5 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0013 | 0/0 | 3183 | 6 | 0 | 2 | 0 | 2 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0014 | 0/0 | 3183 | 5 | 1 | 3 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0015 | 0/0 | 3216 | 5 | 0 | 1 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0016 | 0/0 | 3183 | 4 | 3 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0017 | 0/0 | 3183 | 3 | 1 | 0 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0018 | 0/0 | 3183 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0019 | 0/0 | 3183 | 3 | 2 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0020 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0021 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0022 | 0/0 | 3183 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0023 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0024 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0025 | 0/0 | 3183 | 2 | 1 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0026 | 0/1 | 3183 | 2 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0027 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0028 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0029 | 0/0 | 3183 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0030 | 0/0 | 3216 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0031 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0032 | 0/0 | 3183 | 2 | 0 | 1 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0033 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0034 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0035 | 0/0 | 3216 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0036 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0037 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0038 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0039 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0040 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0041 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0042 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0043 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0044 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0045 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0046 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0047 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0048 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0049 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0050 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0051 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0052 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0053 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0054 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0055 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0056 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0057 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0058 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0059 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0060 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0061 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0062 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0063 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0064 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0065 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0066 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0067 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0068 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0069 | 0/0 | 3216 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0070 | 0/0 | 3216 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
c0071 | 0/0 | 3216 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
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 | 1/0 | 1304 | 116 | 27 | 23 | 36 | 7 | 22 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0002 | 0/0 | 1304 | 102 | 23 | 21 | 44 | 4 | 10 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0003 | 0/1 | 1304 | 79 | 19 | 15 | 37 | 2 | 5 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0004 | 0/0 | 1304 | 74 | 1 | 10 | 58 | 1 | 4 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0005 | 0/0 | 1304 | 8 | 7 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0006 | 0/0 | 1304 | 7 | 6 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0007 | 0/0 | 1304 | 4 | 1 | 3 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0008 | 0/0 | 1304 | 4 | 0 | 0 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0009 | 0/0 | 1304 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0010 | 0/0 | 1304 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0011 | 0/0 | 1304 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0012 | 0/0 | 1304 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0013 | 0/0 | 1304 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0014 | 0/0 | 1304 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0015 | 0/0 | 1304 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0016 | 0/0 | 1304 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0017 | 0/0 | 1304 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0018 | 0/0 | 1304 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0019 | 0/0 | 1304 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
t0020 | 0/0 | 1304 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
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 | 7 | 0 | 0 | 3 | 2 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0002 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0006 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0007 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0004 | 0/0 | 3183 | 28 | 1 | 4 | 20 | 0 | 3 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0005 | 0/0 | 3183 | 28 | 3 | 2 | 17 | 0 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0006 | 0/0 | 3183 | 26 | 4 | 12 | 1 | 3 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0007 | 0/0 | 3183 | 17 | 9 | 6 | 1 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0013 | 0/0 | 3183 | 6 | 0 | 2 | 0 | 2 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0017 | 0/0 | 3183 | 3 | 1 | 0 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0021 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0036 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0048 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0052 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0053 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0061 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0063 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0065 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0002c0001 | 0/0 | 3183 | 68 | 15 | 13 | 27 | 4 | 9 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0003 | 0/0 | 3183 | 44 | 1 | 11 | 27 | 0 | 5 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0008 | 0/0 | 3183 | 17 | 14 | 1 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0018 | 0/0 | 3183 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0026 | 0/1 | 3183 | 2 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0055 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0057 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0002 | 0/0 | 3183 | 44 | 1 | 9 | 29 | 0 | 5 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0010 | 0/0 | 3183 | 10 | 0 | 0 | 10 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0027 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0067 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0005c0011 | 0/0 | 3183 | 8 | 6 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0005c0016 | 0/0 | 3183 | 4 | 3 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0005c0054 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0006c0009 | 0/0 | 3183 | 11 | 0 | 0 | 10 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0007c0014 | 0/0 | 3183 | 5 | 1 | 3 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0007c0029 | 0/0 | 3183 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0007c0034 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0007c0049 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0008c0012 | 1/0 | 3183 | 7 | 1 | 0 | 5 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0008c0041 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0008c0044 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0009c0015 | 0/0 | 3216 | 5 | 0 | 1 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0009c0030 | 0/0 | 3216 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0010c0020 | 0/0 | 3183 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0011c0025 | 0/0 | 3183 | 2 | 1 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0011c0050 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0012c0019 | 0/0 | 3183 | 3 | 2 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0013c0031 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0014c0035 | 0/0 | 3216 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0015c0022 | 0/0 | 3183 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0016c0033 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0017c0047 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0017c0062 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0018c0028 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0019c0024 | 0/0 | 3183 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0020c0045 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0020c0068 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0021c0023 | 0/0 | 3183 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0022c0032 | 0/0 | 3183 | 2 | 0 | 1 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0023c0071 | 0/0 | 3216 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0024c0038 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0025c0070 | 0/0 | 3216 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0026c0069 | 0/0 | 3216 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0027c0042 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0028c0043 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0029c0040 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0030c0039 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0031c0051 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0032c0046 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0033c0060 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0034c0059 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0035c0058 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0036c0064 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0037c0056 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0038c0066 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0039c0037 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0004t0001 | 0/0 | 4486 | 19 | 1 | 3 | 12 | 0 | 3 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0004t0004 | 0/0 | 4486 | 9 | 0 | 1 | 8 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0005t0001 | 0/0 | 4486 | 20 | 3 | 1 | 10 | 0 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0005t0002 | 0/0 | 4486 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0005t0004 | 0/0 | 4486 | 4 | 0 | 0 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0005t0017 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0006t0001 | 0/0 | 4486 | 24 | 3 | 11 | 1 | 3 | 6 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0006t0007 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0006t0018 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0007t0001 | 0/0 | 4486 | 11 | 5 | 4 | 1 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0007t0006 | 0/0 | 4486 | 5 | 4 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0007t0007 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0013t0001 | 0/0 | 4486 | 6 | 0 | 2 | 0 | 2 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0017t0001 | 0/0 | 4486 | 3 | 1 | 0 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0021t0001 | 0/0 | 4486 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0036t0001 | 0/0 | 4486 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0048t0001 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0052t0012 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0053t0001 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0061t0001 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0063t0001 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0001c0065t0001 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0002c0001t0002 | 0/0 | 4486 | 66 | 15 | 11 | 27 | 4 | 9 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0002c0001t0014 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0002c0001t0020 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0003t0003 | 0/0 | 4486 | 42 | 1 | 11 | 26 | 0 | 4 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0003t0013 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0003t0015 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0008t0003 | 0/0 | 4486 | 17 | 14 | 1 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0018t0003 | 0/0 | 4486 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0026t0003 | 0/1 | 4486 | 2 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0055t0003 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0003c0057t0003 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0002t0001 | 0/0 | 4486 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0002t0004 | 0/0 | 4486 | 39 | 1 | 9 | 25 | 0 | 4 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0002t0008 | 0/0 | 4486 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0002t0009 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0010t0002 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0010t0004 | 0/0 | 4486 | 7 | 0 | 0 | 7 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0010t0008 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0010t0009 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0027t0006 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0027t0019 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0004c0067t0008 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0005c0011t0002 | 0/0 | 4486 | 8 | 6 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0005c0016t0002 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0005c0016t0003 | 0/0 | 4486 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0005c0016t0005 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0005c0054t0005 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0006c0009t0004 | 0/0 | 4486 | 11 | 0 | 0 | 10 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0007c0014t0002 | 0/0 | 4486 | 5 | 1 | 3 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0007c0029t0002 | 0/0 | 4486 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0007c0034t0002 | 0/0 | 4486 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0007c0049t0002 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0008c0012t0001 | 1/0 | 4486 | 6 | 0 | 0 | 5 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0008c0012t0011 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0008c0041t0007 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0008c0044t0001 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0009c0015t0002 | 0/0 | 4519 | 5 | 0 | 1 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0009c0030t0002 | 0/0 | 4519 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0010c0020t0001 | 0/0 | 4486 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0011c0025t0005 | 0/0 | 4486 | 2 | 1 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0011c0050t0005 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0012c0019t0001 | 0/0 | 4486 | 2 | 1 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0012c0019t0006 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0013c0031t0001 | 0/0 | 4486 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0014c0035t0002 | 0/0 | 4519 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0015c0022t0003 | 0/0 | 4486 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0016c0033t0003 | 0/0 | 4486 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0017c0047t0004 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0017c0062t0004 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0018c0028t0005 | 0/0 | 4486 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0019c0024t0010 | 0/0 | 4486 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0020c0045t0002 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0020c0068t0002 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0021c0023t0001 | 0/0 | 4486 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0022c0032t0003 | 0/0 | 4486 | 2 | 0 | 1 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0023c0071t0002 | 0/0 | 4519 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0024c0038t0001 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0025c0070t0002 | 0/0 | 4519 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0026c0069t0001 | 0/0 | 4519 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0027c0042t0005 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0028c0043t0003 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0029c0040t0001 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0030c0039t0004 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0031c0051t0007 | 0/0 | 4486 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0032c0046t0001 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0033c0060t0001 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0034c0059t0003 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0035c0058t0004 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0036c0064t0003 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0037c0056t0016 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0038c0066t0003 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
a0039c0037t0003 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | copy fasta | chr1 | 177923788 | 177975058 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0004t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0004t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0004g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0005t0017g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0006 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0007 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0006t0018g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0006g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0006g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0007t0007g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0013t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0013t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0013t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0013t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0017t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0017t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0017t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0021t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0021t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0021t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0036t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0036t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0048t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0052t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0053t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0061t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0063t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0001c0065t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 3 | 2 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0014g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0002c0001t0020g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0002 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0013g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0003t0015g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0008t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0018t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0018t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0018t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0026t0003g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0026t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0055t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0003c0057t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0008g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0002t0009g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0004g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0008g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0010t0009g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0027t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0027t0019g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0004c0067t0008g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0011t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0011t0002g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0011t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0011t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0016t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0016t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0016t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0016t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0005c0054t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0006c0009t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0014t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0014t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0014t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0014t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0014t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0029t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0029t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0034t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0034t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0007c0049t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0001g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0012t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0041t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0008c0044t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0015t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0015t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0015t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0015t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0030t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0009c0030t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0010c0020t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0010c0020t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0011c0025t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0011c0025t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0011c0050t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0012c0019t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0012c0019t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0012c0019t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0013c0031t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0013c0031t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0014c0035t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0014c0035t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0015c0022t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0015c0022t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0016c0033t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0017c0047t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0017c0062t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0018c0028t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0019c0024t0010g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0019c0024t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0020c0045t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0020c0068t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0021c0023t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0021c0023t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0022c0032t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0022c0032t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0023c0071t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0024c0038t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0025c0070t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0026c0069t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0027c0042t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0028c0043t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0029c0040t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0030c0039t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0031c0051t0007g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0032c0046t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0033c0060t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0034c0059t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0035c0058t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0036c0064t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0037c0056t0016g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0038c0066t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
a0039c0037t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0022 | c0032 | t0003 | g0134 | EUR | GBR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00099 | hp2 | a0001 | c0006 | t0001 | g0007 | EUR | GBR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00140 | hp1 | a0001 | c0048 | t0001 | g0129 | EUR | GBR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00140 | hp2 | a0002 | c0001 | t0002 | g0029 | EUR | GBR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00280 | hp1 | a0001 | c0006 | t0001 | g0179 | EUR | FIN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00280 | hp2 | a0006 | c0009 | t0004 | g0141 | EUR | FIN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00323 | hp1 | a0002 | c0001 | t0002 | g0001 | EUR | FIN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00323 | hp2 | a0001 | c0006 | t0001 | g0007 | EUR | FIN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00408 | hp1 | a0003 | c0003 | t0003 | g0078 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00408 | hp2 | a0004 | c0002 | t0004 | g0037 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00423 | hp1 | a0006 | c0009 | t0004 | g0314 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00423 | hp2 | a0023 | c0071 | t0002 | g0219 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00438 | hp1 | a0002 | c0001 | t0002 | g0325 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00438 | hp2 | a0001 | c0065 | t0001 | g0299 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00544 | hp1 | a0003 | c0003 | t0003 | g0079 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00544 | hp2 | a0017 | c0047 | t0004 | g0127 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00558 | hp1 | a0003 | c0003 | t0003 | g0296 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00558 | hp2 | a0004 | c0067 | t0008 | g0213 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00597 | hp1 | a0001 | c0005 | t0002 | g0293 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00597 | hp2 | a0002 | c0001 | t0002 | g0315 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00609 | hp1 | a0026 | c0069 | t0001 | g0214 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00609 | hp2 | a0004 | c0010 | t0002 | g0298 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00621 | hp1 | a0004 | c0002 | t0004 | g0033 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00621 | hp2 | a0001 | c0004 | t0001 | g0261 | EAS | CHS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00639 | hp1 | a0001 | c0004 | t0001 | g0280 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00639 | hp2 | a0001 | c0007 | t0001 | g0014 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00642 | hp1 | a0001 | c0007 | t0001 | g0014 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00642 | hp2 | a0007 | c0029 | t0002 | g0223 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00733 | hp1 | a0001 | c0007 | t0007 | g0307 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00733 | hp2 | a0007 | c0014 | t0002 | g0172 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00735 | hp1 | a0028 | c0043 | t0003 | g0151 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00735 | hp2 | a0002 | c0001 | t0002 | g0125 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00738 | hp1 | a0001 | c0005 | t0001 | g0083 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00738 | hp2 | a0025 | c0070 | t0002 | g0217 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00741 | hp1 | a0003 | c0026 | t0003 | g0235 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG00741 | hp2 | a0001 | c0006 | t0001 | g0007 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01069 | hp1 | a0001 | c0007 | t0006 | g0019 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01069 | hp2 | a0003 | c0003 | t0003 | g0002 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01070 | hp1 | a0005 | c0011 | t0002 | g0011 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01070 | hp2 | a0001 | c0006 | t0001 | g0190 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01071 | hp1 | a0005 | c0011 | t0002 | g0011 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01071 | hp2 | a0003 | c0003 | t0003 | g0002 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01074 | hp1 | a0031 | c0051 | t0007 | g0056 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01074 | hp2 | a0002 | c0001 | t0002 | g0013 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01081 | hp1 | a0001 | c0007 | t0001 | g0193 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01081 | hp2 | a0001 | c0006 | t0001 | g0006 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01099 | hp1 | a0011 | c0025 | t0005 | g0185 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01099 | hp2 | a0007 | c0029 | t0002 | g0194 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01106 | hp1 | a0003 | c0003 | t0003 | g0108 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01106 | hp2 | a0001 | c0006 | t0001 | g0222 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01109 | hp1 | a0005 | c0016 | t0002 | g0246 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01109 | hp2 | a0001 | c0004 | t0001 | g0139 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01168 | hp1 | a0001 | c0013 | t0001 | g0028 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01168 | hp2 | a0007 | c0014 | t0002 | g0086 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01169 | hp1 | a0001 | c0013 | t0001 | g0028 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01169 | hp2 | a0001 | c0004 | t0001 | g0071 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01175 | hp1 | a0008 | c0041 | t0007 | g0156 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01175 | hp2 | a0001 | c0007 | t0001 | g0117 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01192 | hp1 | a0001 | c0006 | t0001 | g0053 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01192 | hp2 | a0002 | c0001 | t0002 | g0008 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01243 | hp1 | a0003 | c0003 | t0003 | g0308 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01243 | hp2 | a0012 | c0019 | t0001 | g0072 | AMR | PUR | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01255 | hp1 | a0003 | c0003 | t0003 | g0038 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01255 | hp2 | a0002 | c0001 | t0014 | g0324 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01257 | hp1 | a0002 | c0001 | t0002 | g0231 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01257 | hp2 | a0003 | c0003 | t0003 | g0047 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01258 | hp1 | a0003 | c0003 | t0003 | g0109 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01258 | hp2 | a0002 | c0001 | t0002 | g0041 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01261 | hp1 | a0009 | c0015 | t0002 | g0218 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01261 | hp2 | a0007 | c0014 | t0002 | g0187 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01346 | hp1 | a0024 | c0038 | t0001 | g0254 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01346 | hp2 | a0001 | c0004 | t0004 | g0281 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01358 | hp1 | a0003 | c0003 | t0003 | g0002 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01358 | hp2 | a0002 | c0001 | t0002 | g0041 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01361 | hp1 | a0004 | c0002 | t0004 | g0180 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01361 | hp2 | a0004 | c0002 | t0004 | g0166 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01433 | hp1 | a0001 | c0006 | t0018 | g0189 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01433 | hp2 | a0004 | c0002 | t0004 | g0164 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01496 | hp1 | a0001 | c0006 | t0001 | g0007 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01496 | hp2 | a0004 | c0002 | t0004 | g0169 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01515 | hp1 | a0001 | c0013 | t0001 | g0023 | EUR | IBS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01515 | hp2 | a0001 | c0007 | t0001 | g0118 | EUR | IBS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01517 | hp1 | a0002 | c0001 | t0002 | g0029 | EUR | IBS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01517 | hp2 | a0001 | c0013 | t0001 | g0023 | EUR | IBS | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01884 | hp1 | a0019 | c0024 | t0010 | g0054 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0057 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01891 | hp1 | a0001 | c0005 | t0001 | g0112 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01891 | hp2 | a0003 | c0008 | t0003 | g0098 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01928 | hp1 | a0001 | c0006 | t0001 | g0120 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01928 | hp2 | a0004 | c0002 | t0004 | g0277 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01943 | hp1 | a0001 | c0006 | t0001 | g0006 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01943 | hp2 | a0002 | c0001 | t0002 | g0008 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01952 | hp1 | a0003 | c0003 | t0003 | g0047 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01952 | hp2 | a0004 | c0002 | t0004 | g0027 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01978 | hp1 | a0002 | c0001 | t0002 | g0148 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01978 | hp2 | a0002 | c0001 | t0002 | g0008 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01981 | hp1 | a0002 | c0001 | t0020 | g0328 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01981 | hp2 | a0004 | c0002 | t0004 | g0116 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01993 | hp1 | a0002 | c0001 | t0002 | g0229 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01993 | hp2 | a0003 | c0003 | t0003 | g0026 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02004 | hp1 | a0002 | c0001 | t0002 | g0126 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02004 | hp2 | a0003 | c0003 | t0003 | g0002 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02027 | hp1 | a0030 | c0039 | t0004 | g0271 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02027 | hp2 | a0002 | c0001 | t0002 | g0157 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02040 | hp1 | a0003 | c0003 | t0015 | g0111 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02040 | hp2 | a0004 | c0002 | t0004 | g0275 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02055 | hp1 | a0003 | c0008 | t0003 | g0058 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02055 | hp2 | a0001 | c0063 | t0001 | g0132 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02071 | hp1 | a0004 | c0002 | t0004 | g0036 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02071 | hp2 | a0002 | c0001 | t0002 | g0226 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02074 | hp1 | a0008 | c0012 | t0001 | g0269 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02074 | hp2 | a0001 | c0004 | t0001 | g0263 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02080 | hp1 | a0017 | c0062 | t0004 | g0285 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02080 | hp2 | a0001 | c0005 | t0001 | g0016 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02083 | hp1 | a0001 | c0004 | t0001 | g0158 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02083 | hp2 | a0004 | c0010 | t0004 | g0200 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02129 | hp1 | a0003 | c0003 | t0003 | g0204 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02129 | hp2 | a0001 | c0053 | t0001 | g0272 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02132 | hp1 | a0001 | c0005 | t0002 | g0110 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02132 | hp2 | a0001 | c0004 | t0001 | g0045 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02135 | hp1 | a0001 | c0005 | t0001 | g0199 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02135 | hp2 | a0004 | c0002 | t0004 | g0183 | EAS | KHV | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02145 | hp1 | a0039 | c0037 | t0003 | g0239 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02145 | hp2 | a0004 | c0027 | t0019 | g0327 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02148 | hp1 | a0004 | c0002 | t0004 | g0234 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02148 | hp2 | a0001 | c0006 | t0001 | g0006 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02155 | hp1 | a0001 | c0004 | t0001 | g0255 | EAS | CDX | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02155 | hp2 | a0002 | c0001 | t0002 | g0228 | EAS | CDX | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02165 | hp1 | a0003 | c0003 | t0003 | g0119 | EAS | CDX | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02165 | hp2 | a0001 | c0004 | t0001 | g0045 | EAS | CDX | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02257 | hp1 | a0005 | c0011 | t0002 | g0010 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02257 | hp2 | a0001 | c0007 | t0001 | g0014 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02258 | hp1 | a0002 | c0001 | t0002 | g0005 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02258 | hp2 | a0001 | c0017 | t0001 | g0061 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02280 | hp1 | a0003 | c0008 | t0003 | g0320 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02280 | hp2 | a0001 | c0007 | t0006 | g0019 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02293 | hp1 | a0001 | c0006 | t0001 | g0173 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02293 | hp2 | a0001 | c0005 | t0017 | g0135 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02300 | hp1 | a0004 | c0002 | t0004 | g0027 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02300 | hp2 | a0022 | c0032 | t0003 | g0286 | AMR | PEL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02451 | hp1 | a0036 | c0064 | t0003 | g0137 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02451 | hp2 | a0005 | c0011 | t0002 | g0010 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02572 | hp1 | a0012 | c0019 | t0006 | g0048 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02572 | hp2 | a0001 | c0005 | t0001 | g0043 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02602 | hp1 | a0003 | c0003 | t0013 | g0211 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02602 | hp2 | a0004 | c0002 | t0001 | g0128 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02615 | hp1 | a0002 | c0001 | t0002 | g0004 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02615 | hp2 | a0001 | c0005 | t0001 | g0043 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02622 | hp1 | a0003 | c0008 | t0003 | g0247 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02622 | hp2 | a0020 | c0068 | t0002 | g0088 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02630 | hp1 | a0029 | c0040 | t0001 | g0095 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02630 | hp2 | a0003 | c0008 | t0003 | g0080 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02698 | hp1 | a0001 | c0006 | t0001 | g0174 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02698 | hp2 | a0001 | c0004 | t0001 | g0091 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02717 | hp1 | a0004 | c0027 | t0006 | g0050 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02717 | hp2 | a0001 | c0007 | t0001 | g0100 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02723 | hp1 | a0005 | c0011 | t0002 | g0011 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02723 | hp2 | a0005 | c0054 | t0005 | g0124 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02735 | hp1 | a0002 | c0001 | t0002 | g0013 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02735 | hp2 | a0007 | c0049 | t0002 | g0188 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02738 | hp1 | a0004 | c0002 | t0004 | g0034 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02738 | hp2 | a0003 | c0003 | t0003 | g0002 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02809 | hp1 | a0007 | c0014 | t0002 | g0186 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02809 | hp2 | a0001 | c0006 | t0007 | g0253 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02818 | hp1 | a0027 | c0042 | t0005 | g0092 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02818 | hp2 | a0001 | c0021 | t0001 | g0278 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02886 | hp1 | a0002 | c0001 | t0002 | g0004 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02886 | hp2 | a0003 | c0008 | t0003 | g0087 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02895 | hp1 | a0003 | c0008 | t0003 | g0241 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02895 | hp2 | a0001 | c0007 | t0001 | g0044 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02896 | hp1 | a0003 | c0008 | t0003 | g0066 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02896 | hp2 | a0001 | c0007 | t0006 | g0018 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02897 | hp1 | a0001 | c0007 | t0006 | g0018 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02897 | hp2 | a0001 | c0007 | t0001 | g0044 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02922 | hp1 | a0005 | c0011 | t0002 | g0010 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02922 | hp2 | a0002 | c0001 | t0002 | g0004 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02965 | hp1 | a0018 | c0028 | t0005 | g0021 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02965 | hp2 | a0001 | c0007 | t0001 | g0242 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02970 | hp1 | a0001 | c0006 | t0001 | g0244 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02970 | hp2 | a0005 | c0016 | t0005 | g0138 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02976 | hp1 | a0002 | c0001 | t0002 | g0005 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02976 | hp2 | a0001 | c0036 | t0001 | g0121 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03041 | hp1 | a0002 | c0001 | t0002 | g0248 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03041 | hp2 | a0003 | c0008 | t0003 | g0067 | AFR | GWD | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03098 | hp1 | a0001 | c0006 | t0001 | g0089 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03098 | hp2 | a0003 | c0008 | t0003 | g0099 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03130 | hp1 | a0010 | c0020 | t0001 | g0020 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03130 | hp2 | a0002 | c0001 | t0002 | g0005 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03139 | hp1 | a0018 | c0028 | t0005 | g0021 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03139 | hp2 | a0003 | c0008 | t0003 | g0243 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03209 | hp1 | a0010 | c0020 | t0001 | g0063 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03209 | hp2 | a0001 | c0021 | t0001 | g0279 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03225 | hp1 | a0010 | c0020 | t0001 | g0020 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03225 | hp2 | a0002 | c0001 | t0002 | g0042 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03239 | hp1 | a0002 | c0001 | t0002 | g0181 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03239 | hp2 | a0002 | c0001 | t0002 | g0265 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03453 | hp1 | a0001 | c0007 | t0006 | g0049 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03453 | hp2 | a0005 | c0016 | t0003 | g0055 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03490 | hp1 | a0001 | c0005 | t0001 | g0313 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03490 | hp2 | a0002 | c0001 | t0002 | g0013 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03491 | hp1 | a0003 | c0003 | t0003 | g0288 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03491 | hp2 | a0002 | c0001 | t0002 | g0001 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03492 | hp1 | a0001 | c0005 | t0001 | g0312 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03492 | hp2 | a0002 | c0001 | t0002 | g0001 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03516 | hp1 | a0005 | c0016 | t0003 | g0252 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03516 | hp2 | a0003 | c0008 | t0003 | g0081 | AFR | ESN | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03579 | hp1 | a0008 | c0044 | t0001 | g0250 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03579 | hp2 | a0005 | c0011 | t0002 | g0060 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03654 | hp1 | a0001 | c0005 | t0001 | g0291 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03654 | hp2 | a0001 | c0013 | t0001 | g0210 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03669 | hp1 | a0004 | c0002 | t0004 | g0168 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03669 | hp2 | a0001 | c0005 | t0001 | g0202 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03688 | hp1 | a0003 | c0003 | t0003 | g0300 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03688 | hp2 | a0001 | c0061 | t0001 | g0289 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03704 | hp1 | a0001 | c0006 | t0001 | g0175 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03704 | hp2 | a0001 | c0006 | t0001 | g0184 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03710 | hp1 | a0004 | c0002 | t0004 | g0162 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03710 | hp2 | a0003 | c0003 | t0003 | g0297 | SAS | PJL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03831 | hp1 | a0001 | c0004 | t0001 | g0260 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03831 | hp2 | a0001 | c0006 | t0001 | g0177 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03834 | hp1 | a0001 | c0004 | t0001 | g0257 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03834 | hp2 | a0002 | c0001 | t0002 | g0154 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03927 | hp1 | a0001 | c0017 | t0001 | g0096 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03927 | hp2 | a0001 | c0006 | t0001 | g0176 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03942 | hp1 | a0001 | c0005 | t0001 | g0294 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03942 | hp2 | a0001 | c0017 | t0001 | g0319 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04115 | hp1 | a0001 | c0006 | t0001 | g0006 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04115 | hp2 | a0002 | c0001 | t0002 | g0149 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04184 | hp1 | a0015 | c0022 | t0003 | g0150 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04184 | hp2 | a0001 | c0013 | t0001 | g0136 | SAS | BEB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04204 | hp1 | a0004 | c0002 | t0004 | g0032 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04204 | hp2 | a0002 | c0001 | t0002 | g0146 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04228 | hp1 | a0001 | c0005 | t0001 | g0016 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG04228 | hp2 | a0032 | c0046 | t0001 | g0170 | SAS | STU | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18522 | hp1 | a0003 | c0008 | t0003 | g0240 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18522 | hp2 | a0005 | c0011 | t0002 | g0123 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18612 | hp1 | a0004 | c0002 | t0004 | g0302 | EAS | CHB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18612 | hp2 | a0003 | c0008 | t0003 | g0103 | EAS | CHB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18906 | hp1 | a0019 | c0024 | t0010 | g0062 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18906 | hp2 | a0002 | c0001 | t0002 | g0004 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18939 | hp1 | a0004 | c0002 | t0004 | g0165 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18939 | hp2 | a0002 | c0001 | t0002 | g0040 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18942 | hp1 | a0004 | c0002 | t0004 | g0003 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18942 | hp2 | a0008 | c0012 | t0001 | g0147 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18943 | hp1 | a0006 | c0009 | t0004 | g0094 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18943 | hp2 | a0002 | c0001 | t0002 | g0224 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18944 | hp1 | a0001 | c0004 | t0004 | g0104 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18944 | hp2 | a0002 | c0001 | t0002 | g0082 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18945 | hp1 | a0002 | c0001 | t0002 | g0143 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18945 | hp2 | a0001 | c0005 | t0001 | g0198 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18946 | hp1 | a0001 | c0004 | t0004 | g0106 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18946 | hp2 | a0001 | c0006 | t0001 | g0097 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18947 | hp1 | a0004 | c0002 | t0004 | g0155 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18947 | hp2 | a0001 | c0005 | t0001 | g0310 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18948 | hp1 | a0003 | c0018 | t0003 | g0306 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18948 | hp2 | a0001 | c0004 | t0001 | g0258 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18949 | hp1 | a0003 | c0008 | t0003 | g0102 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18949 | hp2 | a0001 | c0004 | t0004 | g0321 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18950 | hp1 | a0004 | c0002 | t0004 | g0163 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18950 | hp2 | a0002 | c0001 | t0002 | g0015 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18951 | hp1 | a0004 | c0002 | t0004 | g0003 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18951 | hp2 | a0008 | c0012 | t0001 | g0153 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18952 | hp1 | a0001 | c0004 | t0004 | g0025 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18952 | hp2 | a0001 | c0005 | t0001 | g0022 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18953 | hp1 | a0004 | c0002 | t0004 | g0159 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18953 | hp2 | a0004 | c0010 | t0004 | g0076 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18954 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0290 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18959 | hp1 | a0004 | c0002 | t0001 | g0221 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18959 | hp2 | a0003 | c0003 | t0003 | g0085 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18960 | hp1 | a0001 | c0004 | t0001 | g0256 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18960 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18961 | hp1 | a0009 | c0030 | t0002 | g0191 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18961 | hp2 | a0004 | c0002 | t0004 | g0003 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18962 | hp1 | a0006 | c0009 | t0004 | g0270 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18962 | hp2 | a0001 | c0005 | t0001 | g0016 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18963 | hp1 | a0002 | c0001 | t0002 | g0267 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18963 | hp2 | a0001 | c0007 | t0001 | g0322 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18964 | hp1 | a0034 | c0059 | t0003 | g0077 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18964 | hp2 | a0009 | c0015 | t0002 | g0039 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18965 | hp1 | a0006 | c0009 | t0004 | g0225 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18965 | hp2 | a0003 | c0003 | t0003 | g0208 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18966 | hp1 | a0014 | c0035 | t0002 | g0318 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18966 | hp2 | a0001 | c0004 | t0001 | g0262 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18969 | hp1 | a0004 | c0010 | t0009 | g0196 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18969 | hp2 | a0006 | c0009 | t0004 | g0145 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18970 | hp1 | a0003 | c0003 | t0003 | g0316 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18970 | hp2 | a0002 | c0001 | t0002 | g0142 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18971 | hp1 | a0004 | c0002 | t0004 | g0161 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18971 | hp2 | a0004 | c0010 | t0008 | g0284 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18974 | hp1 | a0002 | c0001 | t0002 | g0301 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18974 | hp2 | a0003 | c0003 | t0003 | g0287 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18975 | hp1 | a0009 | c0030 | t0002 | g0192 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18975 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18977 | hp1 | a0002 | c0001 | t0002 | g0311 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18977 | hp2 | a0008 | c0012 | t0001 | g0030 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18979 | hp1 | a0003 | c0003 | t0003 | g0292 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18979 | hp2 | a0001 | c0004 | t0001 | g0264 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18981 | hp1 | a0004 | c0002 | t0004 | g0035 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18981 | hp2 | a0001 | c0005 | t0004 | g0017 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18982 | hp1 | a0004 | c0010 | t0004 | g0074 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18982 | hp2 | a0003 | c0003 | t0003 | g0203 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18983 | hp1 | a0007 | c0034 | t0002 | g0133 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18983 | hp2 | a0004 | c0002 | t0004 | g0032 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18986 | hp1 | a0001 | c0005 | t0002 | g0236 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18986 | hp2 | a0004 | c0002 | t0008 | g0031 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18987 | hp1 | a0016 | c0033 | t0003 | g0046 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18987 | hp2 | a0006 | c0009 | t0004 | g0266 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18988 | hp1 | a0014 | c0035 | t0002 | g0317 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18988 | hp2 | a0003 | c0018 | t0003 | g0232 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18989 | hp1 | a0006 | c0009 | t0004 | g0009 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18989 | hp2 | a0001 | c0005 | t0001 | g0107 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18990 | hp1 | a0003 | c0003 | t0003 | g0114 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18990 | hp2 | a0004 | c0002 | t0004 | g0037 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18993 | hp1 | a0002 | c0001 | t0002 | g0144 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18993 | hp2 | a0001 | c0004 | t0004 | g0025 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18995 | hp1 | a0003 | c0003 | t0003 | g0295 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA18995 | hp2 | a0004 | c0010 | t0004 | g0012 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19000 | hp1 | a0003 | c0003 | t0003 | g0205 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19000 | hp2 | a0002 | c0001 | t0002 | g0268 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19002 | hp1 | a0004 | c0010 | t0004 | g0012 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19002 | hp2 | a0015 | c0022 | t0003 | g0227 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19005 | hp1 | a0003 | c0003 | t0003 | g0026 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19005 | hp2 | a0035 | c0058 | t0004 | g0075 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19009 | hp1 | a0006 | c0009 | t0004 | g0009 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19009 | hp2 | a0004 | c0002 | t0008 | g0031 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19010 | hp1 | a0006 | c0009 | t0004 | g0009 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19010 | hp2 | a0002 | c0001 | t0002 | g0274 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19011 | hp1 | a0001 | c0004 | t0004 | g0024 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19011 | hp2 | a0001 | c0005 | t0001 | g0022 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19012 | hp1 | a0009 | c0015 | t0002 | g0216 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19012 | hp2 | a0007 | c0034 | t0002 | g0309 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19043 | hp1 | a0001 | c0021 | t0001 | g0326 | AFR | LWK | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19043 | hp2 | a0008 | c0012 | t0011 | g0068 | AFR | LWK | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19054 | hp1 | a0004 | c0002 | t0004 | g0033 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19054 | hp2 | a0006 | c0009 | t0004 | g0009 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19057 | hp1 | a0003 | c0003 | t0003 | g0113 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19057 | hp2 | a0004 | c0002 | t0004 | g0003 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19058 | hp1 | a0003 | c0057 | t0003 | g0206 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19058 | hp2 | a0001 | c0004 | t0001 | g0259 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19060 | hp1 | a0001 | c0005 | t0004 | g0017 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19060 | hp2 | a0004 | c0010 | t0004 | g0012 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19062 | hp1 | a0016 | c0033 | t0003 | g0046 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19062 | hp2 | a0004 | c0002 | t0004 | g0035 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19063 | hp1 | a0001 | c0005 | t0001 | g0201 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19063 | hp2 | a0004 | c0002 | t0004 | g0131 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19064 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19064 | hp2 | a0002 | c0001 | t0002 | g0220 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19065 | hp1 | a0003 | c0018 | t0003 | g0182 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19065 | hp2 | a0003 | c0003 | t0003 | g0283 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19067 | hp1 | a0001 | c0004 | t0004 | g0024 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19067 | hp2 | a0021 | c0023 | t0001 | g0303 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19068 | hp1 | a0001 | c0005 | t0004 | g0209 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19068 | hp2 | a0004 | c0002 | t0004 | g0160 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19070 | hp1 | a0004 | c0002 | t0004 | g0036 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19070 | hp2 | a0009 | c0015 | t0002 | g0215 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19072 | hp1 | a0004 | c0002 | t0004 | g0034 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19072 | hp2 | a0020 | c0045 | t0002 | g0233 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19074 | hp1 | a0002 | c0001 | t0002 | g0008 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19074 | hp2 | a0004 | c0010 | t0004 | g0073 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19077 | hp1 | a0001 | c0004 | t0004 | g0101 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19077 | hp2 | a0004 | c0002 | t0009 | g0167 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19079 | hp1 | a0003 | c0003 | t0003 | g0237 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19079 | hp2 | a0003 | c0003 | t0003 | g0282 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19080 | hp1 | a0003 | c0003 | t0003 | g0084 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19080 | hp2 | a0002 | c0001 | t0002 | g0015 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19081 | hp1 | a0001 | c0005 | t0001 | g0195 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19081 | hp2 | a0004 | c0002 | t0004 | g0003 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19082 | hp1 | a0003 | c0003 | t0003 | g0038 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19082 | hp2 | a0002 | c0001 | t0002 | g0273 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19083 | hp1 | a0008 | c0012 | t0001 | g0030 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19083 | hp2 | a0002 | c0001 | t0002 | g0015 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19084 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19084 | hp2 | a0001 | c0004 | t0001 | g0105 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19085 | hp1 | a0003 | c0003 | t0003 | g0207 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19085 | hp2 | a0021 | c0023 | t0001 | g0304 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19088 | hp1 | a0033 | c0060 | t0001 | g0197 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19088 | hp2 | a0007 | c0014 | t0002 | g0171 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19089 | hp1 | a0002 | c0001 | t0002 | g0093 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19089 | hp2 | a0038 | c0066 | t0003 | g0212 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19090 | hp1 | a0009 | c0015 | t0002 | g0039 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19090 | hp2 | a0003 | c0003 | t0003 | g0238 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19091 | hp1 | a0002 | c0001 | t0002 | g0040 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19091 | hp2 | a0001 | c0005 | t0004 | g0017 | EAS | JPT | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19240 | hp1 | a0001 | c0052 | t0012 | g0052 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA19240 | hp2 | a0013 | c0031 | t0001 | g0064 | AFR | YRI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20129 | hp1 | a0002 | c0001 | t0002 | g0042 | AFR | ASW | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20129 | hp2 | a0004 | c0002 | t0004 | g0276 | AFR | ASW | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20805 | hp1 | a0002 | c0001 | t0002 | g0001 | EUR | TSI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20805 | hp2 | a0003 | c0055 | t0003 | g0323 | EUR | TSI | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01123 | hp1 | a0003 | c0008 | t0003 | g0130 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG01123 | hp2 | a0001 | c0006 | t0001 | g0305 | AMR | CLM | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02109 | hp1 | a0011 | c0025 | t0005 | g0251 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02109 | hp2 | a0002 | c0001 | t0002 | g0249 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02486 | hp1 | a0011 | c0050 | t0005 | g0059 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02486 | hp2 | a0013 | c0031 | t0001 | g0051 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02559 | hp1 | a0012 | c0019 | t0001 | g0245 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG02559 | hp2 | a0003 | c0008 | t0003 | g0065 | AFR | ACB | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03471 | hp1 | a0001 | c0036 | t0001 | g0122 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG03471 | hp2 | a0002 | c0001 | t0002 | g0005 | AFR | MSL | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG06807 | hp1 | a0002 | c0001 | t0002 | g0140 | AFR | USA | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
HG06807 | hp2 | a0001 | c0006 | t0001 | g0070 | AFR | USA | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20300 | hp1 | a0003 | c0003 | t0003 | g0090 | AFR | USA | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA20300 | hp2 | a0002 | c0001 | t0002 | g0230 | AFR | USA | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA21309 | hp1 | a0002 | c0001 | t0002 | g0069 | AFR | LWK | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
NA21309 | hp2 | a0037 | c0056 | t0016 | g0115 | AFR | LWK | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
homoSapiens_chm13v2 | hp1 | a0003 | c0026 | t0003 | g0178 | REF | REF | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
homoSapiens_grch38 | hp1 | a0008 | c0012 | t0001 | g0152 | REF | REF | SEC16B_chr1_177923788_177975058 | SEC16B | chr1 | 177923788 | 177975058 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177930564
|
T | C | 3 | a0010a0012a0029 | 7 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
missense_variant | MODERATE | c.3092A>G | p.Asn1031Ser | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/26 | 3325/4486 | 3092/3183 | 1031/1060 | chr1 | 177930564 | ||
chr1:177932503
|
A | G | 1 | a0019 | 2 | HG01884.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.2999T>C | p.Leu1000Ser | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/26 | 3232/4486 | 2999/3183 | 1000/1060 | chr1 | 177932503 | ||
chr1:177933233
|
G | A | 2 | a0018a0027 | 3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.2804C>T | p.Ser935Leu | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 3037/4486 | 2804/3183 | 935/1060 | chr1 | 177933233 | ||
chr1:177933252
|
C | A | 10 | a0002a0005a0007others(7): Show | 104 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
missense_variant | MODERATE | c.2785G>T | p.Ala929Ser | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 3018/4486 | 2785/3183 | 929/1060 | chr1 | 177933252 | ||
chr1:177933278
|
G | A | 1 | a0035 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.2759C>T | p.Ser920Leu | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 2992/4486 | 2759/3183 | 920/1060 | chr1 | 177933278 | ||
chr1:177933590
|
C | T | 9 | a0002a0005a0007others(6): Show | 101 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(98): Show |
missense_variant | MODERATE | c.2618G>A | p.Ser873Asn | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 21/26 | 2851/4486 | 2618/3183 | 873/1060 | chr1 | 177933590 | ||
chr1:177933618
|
G | C | 18 | a0002a0003a0005others(15): Show | 180 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
missense_variant | MODERATE | c.2590C>G | p.Pro864Ala | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 21/26 | 2823/4486 | 2590/3183 | 864/1060 | chr1 | 177933618 | ||
chr1:177936334
|
C | A | 6 | a0002a0006a0007others(3): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
missense_variant | MODERATE | c.2535G>T | p.Gln845His | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/26 | 2768/4486 | 2535/3183 | 845/1060 | chr1 | 177936334 | ||
chr1:177936351
|
A | T | 1 | a0033 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.2518T>A | p.Ser840Thr | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/26 | 2751/4486 | 2518/3183 | 840/1060 | chr1 | 177936351 | ||
chr1:177937372
|
G | A | 1 | a0011 | 3 | HG01099.hp1 HG02109.hp1 HG02486.hp1 |
missense_variant | MODERATE | c.2345C>T | p.Ser782Phe | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/26 | 2578/4486 | 2345/3183 | 782/1060 | chr1 | 177937372 | ||
chr1:177939710
|
G | T | 1 | a0032 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.2195C>A | p.Thr732Lys | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/26 | 2428/4486 | 2195/3183 | 732/1060 | chr1 | 177939710 | ||
chr1:177939717
|
C | T | 8 | a0004a0009a0014others(5): Show | 72 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(69): Show |
missense_variant | MODERATE | c.2188G>A | p.Gly730Arg | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/26 | 2421/4486 | 2188/3183 | 730/1060 | chr1 | 177939717 | ||
chr1:177939725
|
G | A | 1 | a0031 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.2180C>T | p.Ser727Leu | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/26 | 2413/4486 | 2180/3183 | 727/1060 | chr1 | 177939725 | ||
chr1:177939758
|
A | G | 1 | a0021 | 2 | NA19067.hp2 NA19085.hp2 |
missense_variant | MODERATE | c.2147T>C | p.Ile716Thr | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/26 | 2380/4486 | 2147/3183 | 716/1060 | chr1 | 177939758 | ||
chr1:177941995
|
C | T | 1 | a0016 | 2 | NA18987.hp1 NA19062.hp1 |
missense_variant | MODERATE | c.1927G>A | p.Val643Met | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/26 | 2160/4486 | 1927/3183 | 643/1060 | chr1 | 177941995 | ||
chr1:177951984
|
G | A | 1 | a0013 | 2 | HG02486.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.1475C>T | p.Thr492Met | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/26 | 1708/4486 | 1475/3183 | 492/1060 | chr1 | 177951984 | ||
chr1:177958344
|
T | C | 1 | a0036 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1153A>G | p.Ile385Val | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/26 | 1386/4486 | 1153/3183 | 385/1060 | chr1 | 177958344 | ||
chr1:177960366
|
C | G | 1 | a0022 | 2 | HG00099.hp1 HG02300.hp2 |
missense_variant | MODERATE | c.974G>C | p.Arg325Thr | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/26 | 1207/4486 | 974/3183 | 325/1060 | chr1 | 177960366 | ||
chr1:177960813
|
A | G | 1 | a0037 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.914T>C | p.Leu305Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/26 | 1147/4486 | 914/3183 | 305/1060 | chr1 | 177960813 | ||
chr1:177960852
|
T | C | 31 | a0001a0003a0004others(28): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
missense_variant | MODERATE | c.875A>G | p.His292Arg | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/26 | 1108/4486 | 875/3183 | 292/1060 | chr1 | 177960852 | ||
chr1:177960892
|
G | GAGGGATG others(26): Show |
5 | a0009a0014a0023others(2): Show | 12 | HG00423.hp2 HG00609.hp1 HG00738.hp2 others(9): Show |
conservative_inframe_insertion | MODERATE | c.802_834dupGGTCCCAA others(25): Show |
p.Pro278_His279insGl others(31): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/26 | 1067/4486 | 834/3183 | 278/1060 | chr1 | 177960892 | ||
chr1:177961698
|
G | A | 2 | a0010a0013 | 5 | HG02486.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
missense_variant | MODERATE | c.679C>T | p.Arg227Cys | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/26 | 912/4486 | 679/3183 | 227/1060 | chr1 | 177961698 | ||
chr1:177965898
|
T | A | 1 | a0038 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.407A>T | p.Glu136Val | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/26 | 640/4486 | 407/3183 | 136/1060 | chr1 | 177965898 | ||
chr1:177967735
|
C | G | 1 | a0024 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.247G>C | p.Val83Leu | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/26 | 480/4486 | 247/3183 | 83/1060 | chr1 | 177967735 | ||
chr1:177967761
|
G | A | 1 | a0023 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.221C>T | p.Ser74Phe | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/26 | 454/4486 | 221/3183 | 74/1060 | chr1 | 177967761 | ||
chr1:177967930
|
C | T | 1 | a0039 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.52G>A | p.Ala18Thr | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/26 | 285/4486 | 52/3183 | 18/1060 | chr1 | 177967930 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177932520
|
G | A | 17 | a0002c0001a0005c0011a0005c0016others(14): Show | 104 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
synonymous_variant | LOW | c.2982C>T | p.Gly994Gly | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/26 | 3215/4486 | 2982/3183 | 994/1060 | chr1 | 177932520 | ||
chr1:177932523
|
C | T | 17 | a0002c0001a0005c0011a0005c0016others(14): Show | 104 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
synonymous_variant | LOW | c.2979G>A | p.Ala993Ala | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/26 | 3212/4486 | 2979/3183 | 993/1060 | chr1 | 177932523 | ||
chr1:177933244
|
G | A | 1 | a0019c0024 | 2 | HG01884.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.2793C>T | p.Asp931Asp | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 3026/4486 | 2793/3183 | 931/1060 | chr1 | 177933244 | ||
chr1:177933253
|
G | A | 7 | a0001c0007a0001c0048a0001c0061others(4): Show | 23 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(20): Show |
synonymous_variant | LOW | c.2784C>T | p.Pro928Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 3017/4486 | 2784/3183 | 928/1060 | chr1 | 177933253 | ||
chr1:177933271
|
G | A | 2 | a0001c0052a0037c0056 | 2 | NA19240.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.2766C>T | p.Pro922Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/26 | 2999/4486 | 2766/3183 | 922/1060 | chr1 | 177933271 | ||
chr1:177937218
|
G | A | 1 | a0001c0036 | 2 | HG02976.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.2499C>T | p.Gly833Gly | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/26 | 2732/4486 | 2499/3183 | 833/1060 | chr1 | 177937218 | ||
chr1:177940655
|
C | T | 1 | a0003c0057 | 1 | NA19058.hp1 | synonymous_variant | LOW | c.2082G>A | p.Arg694Arg | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/26 | 2315/4486 | 2082/3183 | 694/1060 | chr1 | 177940655 | ||
chr1:177954305
|
T | G | 12 | a0001c0006a0001c0013a0001c0048others(9): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(43): Show |
synonymous_variant | LOW | c.1437A>C | p.Pro479Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/26 | 1670/4486 | 1437/3183 | 479/1060 | chr1 | 177954305 | ||
chr1:177960386
|
G | A | 6 | a0009c0015a0009c0030a0014c0035others(3): Show | 12 | HG00423.hp2 HG00609.hp1 HG00738.hp2 others(9): Show |
synonymous_variant | LOW | c.954C>T | p.Ser318Ser | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/26 | 1187/4486 | 954/3183 | 318/1060 | chr1 | 177960386 | ||
chr1:177960805
|
G | A | 21 | a0001c0004a0001c0007a0001c0021others(18): Show | 98 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(95): Show |
synonymous_variant | LOW | c.922C>T | p.Leu308Leu | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/26 | 1155/4486 | 922/3183 | 308/1060 | chr1 | 177960805 | ||
chr1:177961729
|
T | A | 2 | a0001c0021a0001c0036 | 5 | HG02818.hp2 HG02976.hp2 HG03209.hp2 others(2): Show |
synonymous_variant | LOW | c.648A>T | p.Ser216Ser | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/26 | 881/4486 | 648/3183 | 216/1060 | chr1 | 177961729 | ||
chr1:177961732
|
T | C | 1 | a0003c0055 | 1 | NA20805.hp2 | splice_region_variant&synonymous_variant | LOW | c.645A>G | p.Pro215Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/26 | 878/4486 | 645/3183 | 215/1060 | chr1 | 177961732 | ||
chr1:177965915
|
T | A | 18 | a0001c0005a0001c0013a0001c0061others(15): Show | 105 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
synonymous_variant | LOW | c.390A>T | p.Pro130Pro | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/26 | 623/4486 | 390/3183 | 130/1060 | chr1 | 177965915 | ||
chr1:177967874
|
G | A | 8 | a0001c0036a0004c0067a0009c0015others(5): Show | 14 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(11): Show |
synonymous_variant | LOW | c.108C>T | p.Val36Val | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/26 | 341/4486 | 108/3183 | 36/1060 | chr1 | 177967874 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177928824
|
T | C | 63 | a0001c0004t0004a0001c0005t0002a0001c0005t0004others(60): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*1034A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 1034 | chr1 | 177928824 | |||||
chr1:177928840
|
C | T | 34 | a0001c0004t0004a0001c0005t0004a0001c0005t0017others(31): Show | 164 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*1018G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 1018 | chr1 | 177928840 | |||||
chr1:177928847
|
G | A | 2 | a0001c0006t0018a0002c0001t0014 | 2 | HG01255.hp2 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1011C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 1011 | chr1 | 177928847 | |||||
chr1:177928980
|
C | T | 1 | a0037c0056t0016 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*878G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 878 | chr1 | 177928980 | |||||
chr1:177928981
|
G | A | 1 | a0003c0003t0015 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*877C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 877 | chr1 | 177928981 | |||||
chr1:177929217
|
A | G | 2 | a0004c0002t0009a0004c0010t0009 | 2 | NA18969.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*641T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 641 | chr1 | 177929217 | |||||
chr1:177929409
|
T | C | 1 | a0019c0024t0010 | 2 | HG01884.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*449A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 449 | chr1 | 177929409 | |||||
chr1:177929421
|
A | T | 1 | a0019c0024t0010 | 2 | HG01884.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*437T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 437 | chr1 | 177929421 | |||||
chr1:177929444
|
G | C | 12 | a0001c0004t0004a0001c0005t0004a0004c0002t0004others(9): Show | 78 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*414C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 414 | chr1 | 177929444 | |||||
chr1:177929526
|
C | T | 6 | a0005c0016t0005a0005c0054t0005a0011c0025t0005others(3): Show | 8 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*332G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 332 | chr1 | 177929526 | |||||
chr1:177929556
|
C | T | 1 | a0003c0003t0013 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*302G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 302 | chr1 | 177929556 | |||||
chr1:177929579
|
C | T | 1 | a0001c0052t0012 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 279 | chr1 | 177929579 | |||||
chr1:177929664
|
C | T | 51 | a0001c0004t0004a0001c0005t0002a0001c0005t0004others(48): Show | 267 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*194G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 194 | chr1 | 177929664 | |||||
chr1:177929710
|
C | A | 3 | a0004c0002t0008a0004c0010t0008a0004c0067t0008 | 4 | HG00558.hp2 NA18971.hp2 NA18986.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*148G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 148 | chr1 | 177929710 | |||||
chr1:177929741
|
C | T | 1 | a0008c0012t0011 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 26/26 | 117 | chr1 | 177929741 | |||||
chr1:177969922
|
C | T | 3 | a0001c0007t0006a0004c0027t0006a0012c0019t0006 | 7 | HG01069.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/26 | 1941 | chr1 | 177969922 | |||||
chr1:177969926
|
G | A | 1 | a0004c0027t0019 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/26 | 1945 | chr1 | 177969926 | |||||
chr1:177970032
|
T | A | 1 | a0002c0001t0020 | 1 | HG01981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-207A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/26 | 2051 | chr1 | 177970032 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177929970
|
A | G | 1 | a0006c0009t0004g0145 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3112-41T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177929970 | ||||||
chr1:177929986
|
G | C | 72 | a0003c0003t0003g0002a0003c0003t0003g0026a0003c0003t0003g0038others(69): Show | 82 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.3112-57C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177929986 | ||||||
chr1:177930147
|
G | T | 2 | a0002c0001t0002g0041a0002c0001t0002g0231 | 3 | HG01257.hp1 HG01258.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.3112-218C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177930147 | ||||||
chr1:177930180
|
A | G | 1 | a0003c0003t0003g0237 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3112-251T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177930180 | ||||||
chr1:177930328
|
A | G | 1 | a0003c0003t0003g0090 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3111+217T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177930328 | ||||||
chr1:177930427
|
C | T | 217 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(214): Show | 277 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.3111+118G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 25/25 | chr1 | 177930427 | ||||||
chr1:177930703
|
G | A | 1 | a0028c0043t0003g0151 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3013-60C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177930703 | ||||||
chr1:177930712
|
A | G | 1 | a0001c0004t0001g0091 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3013-69T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177930712 | ||||||
chr1:177930722
|
T | C | 1 | a0004c0002t0004g0165 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3013-79A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177930722 | ||||||
chr1:177930963
|
T | C | 132 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(129): Show | 163 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.3013-320A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177930963 | ||||||
chr1:177931006
|
A | G | 1 | a0001c0006t0001g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3013-363T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931006 | ||||||
chr1:177931160
|
C | T | 7 | a0005c0016t0005g0138a0005c0054t0005g0124a0011c0025t0005g0185others(4): Show | 7 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3013-517G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931160 | ||||||
chr1:177931211
|
G | A | 6 | a0001c0017t0001g0061a0001c0021t0001g0278a0001c0021t0001g0279others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013-568C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931211 | ||||||
chr1:177931255
|
A | G | 1 | a0002c0001t0002g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3013-612T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931255 | ||||||
chr1:177931396
|
A | G | 7 | a0005c0016t0005g0138a0005c0054t0005g0124a0011c0025t0005g0185others(4): Show | 8 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3013-753T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931396 | ||||||
chr1:177931405
|
T | TAG | 5 | a0002c0001t0002g0082a0002c0001t0002g0142a0002c0001t0002g0267others(2): Show | 5 | NA18944.hp2 NA18963.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013-764_3013-763d others(4): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931405 | ||||||
chr1:177931445
|
T | TA | 3 | a0001c0005t0004g0209a0004c0010t0004g0012a0004c0010t0004g0073 | 5 | NA18995.hp2 NA19002.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013-803dupT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931445 | ||||||
chr1:177931481
|
C | T | 217 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(214): Show | 277 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.3013-838G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931481 | ||||||
chr1:177931525
|
C | T | 7 | a0005c0016t0005g0138a0005c0054t0005g0124a0011c0025t0005g0185others(4): Show | 8 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3013-882G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931525 | ||||||
chr1:177931532
|
A | G | 1 | a0001c0021t0001g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3013-889T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931532 | ||||||
chr1:177931858
|
C | T | 1 | a0001c0004t0001g0256 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3012+632G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931858 | ||||||
chr1:177931885
|
C | T | 2 | a0003c0008t0003g0087a0039c0037t0003g0239 | 2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3012+605G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931885 | ||||||
chr1:177931964
|
A | G | 1 | a0020c0068t0002g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3012+526T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931964 | ||||||
chr1:177931985
|
G | GA | 9 | a0001c0006t0007g0253a0005c0016t0005g0138a0005c0054t0005g0124others(6): Show | 10 | HG01074.hp1 HG01099.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3012+504dupT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177931985 | ||||||
chr1:177932161
|
A | G | 4 | a0001c0005t0001g0198a0001c0005t0001g0294a0001c0006t0001g0053others(1): Show | 4 | HG01192.hp1 HG03942.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.3012+329T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932161 | ||||||
chr1:177932179
|
C | T | 1 | a0004c0002t0004g0163 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3012+311G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932179 | ||||||
chr1:177932343
|
CT | C | 2 | a0018c0028t0005g0021a0027c0042t0005g0092 | 3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3012+146delA | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932343 | ||||||
chr1:177932428
|
T | A | 5 | a0005c0016t0005g0138a0005c0054t0005g0124a0011c0025t0005g0185others(2): Show | 5 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3012+62A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932428 | ||||||
chr1:177932438
|
A | G | 1 | a0001c0013t0001g0136 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3012+52T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932438 | ||||||
chr1:177932484
|
G | A | 65 | a0002c0001t0002g0001a0002c0001t0002g0004a0002c0001t0002g0005others(62): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
splice_region_variant&intron_variant | LOW | c.3012+6C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 24/25 | chr1 | 177932484 | ||||||
chr1:177932578
|
T | C | 145 | a0002c0001t0002g0001a0002c0001t0002g0004a0002c0001t0002g0005others(142): Show | 183 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2933-9A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 23/25 | chr1 | 177932578 | ||||||
chr1:177932606
|
A | G | 194 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(191): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.2933-37T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 23/25 | chr1 | 177932606 | ||||||
chr1:177932642
|
C | T | 3 | a0001c0005t0004g0209a0004c0010t0004g0012a0004c0010t0004g0073 | 5 | NA18995.hp2 NA19002.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.2932+56G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 23/25 | chr1 | 177932642 | ||||||
chr1:177932692
|
C | T | 1 | a0001c0063t0001g0132 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.2932+6G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 23/25 | chr1 | 177932692 | ||||||
chr1:177933003
|
A | G | 3 | a0001c0021t0001g0326a0001c0036t0001g0121a0001c0036t0001g0122 | 3 | HG02976.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2824-197T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/25 | chr1 | 177933003 | ||||||
chr1:177933114
|
G | A | 1 | a0024c0038t0001g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2823+100C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 22/25 | chr1 | 177933114 | ||||||
chr1:177933347
|
G | A | 76 | a0002c0001t0002g0001a0002c0001t0002g0004a0002c0001t0002g0005others(73): Show | 104 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2725-35C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 21/25 | chr1 | 177933347 | ||||||
chr1:177933875
|
C | T | 1 | a0003c0008t0003g0247 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2572-239G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933875 | ||||||
chr1:177933969
|
A | C | 70 | a0001c0017t0001g0061a0002c0001t0002g0001a0002c0001t0002g0004others(67): Show | 98 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2572-333T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933969 | ||||||
chr1:177933987
|
G | GC | 5 | a0002c0001t0002g0226a0002c0001t0002g0268a0002c0001t0002g0274others(2): Show | 6 | HG02071.hp2 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2572-352dupG | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933987 | ||||||
chr1:177933989
|
T | C | 70 | a0001c0017t0001g0061a0002c0001t0002g0001a0002c0001t0002g0004others(67): Show | 98 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2572-353A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933989 | ||||||
chr1:177933995
|
C | CA | 9 | a0001c0005t0002g0110a0001c0005t0002g0293a0001c0021t0001g0326others(6): Show | 9 | HG00597.hp1 HG02055.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2572-360dupT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933995 | ||||||
chr1:177933996
|
A | C | 217 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(214): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.2572-360T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933996 | ||||||
chr1:177933997
|
A | C | 3 | a0001c0006t0001g0070a0001c0007t0001g0117a0005c0011t0002g0060 | 3 | HG01175.hp2 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2572-361T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177933997 | ||||||
chr1:177934135
|
CT | C | 65 | a0001c0006t0001g0305a0001c0017t0001g0061a0002c0001t0002g0001others(62): Show | 89 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.2572-500delA | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934135 | ||||||
chr1:177934146
|
T | A | 239 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(236): Show | 290 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.2572-510A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934146 | ||||||
chr1:177934147
|
T | C | 1 | a0001c0006t0001g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2572-511A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934147 | ||||||
chr1:177934234
|
C | T | 1 | a0004c0027t0019g0327 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2572-598G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934234 | ||||||
chr1:177934239
|
A | T | 2 | a0001c0036t0001g0121a0001c0036t0001g0122 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2572-603T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934239 | ||||||
chr1:177934443
|
T | C | 30 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(27): Show | 37 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.2572-807A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934443 | ||||||
chr1:177934624
|
A | G | 4 | a0001c0005t0001g0195a0001c0005t0001g0199a0001c0005t0001g0201others(1): Show | 4 | HG00609.hp1 HG02135.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.2572-988T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934624 | ||||||
chr1:177934661
|
C | T | 35 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(32): Show | 40 | HG00609.hp1 HG00621.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.2572-1025G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934661 | ||||||
chr1:177934707
|
T | G | 1 | a0001c0006t0001g0120 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2572-1071A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934707 | ||||||
chr1:177934708
|
G | C | 1 | a0001c0052t0012g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2572-1072C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934708 | ||||||
chr1:177934976
|
C | T | 3 | a0011c0025t0005g0185a0011c0025t0005g0251a0011c0050t0005g0059 | 3 | HG01099.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2571+1322G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177934976 | ||||||
chr1:177935105
|
G | T | 34 | a0001c0004t0001g0280a0001c0005t0001g0022a0001c0005t0001g0107others(31): Show | 40 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.2571+1193C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935105 | ||||||
chr1:177935194
|
G | A | 3 | a0001c0063t0001g0132a0005c0016t0005g0138a0005c0054t0005g0124 | 3 | HG02055.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2571+1104C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935194 | ||||||
chr1:177935267
|
ATGCCTCC others(8): Show |
A | 6 | a0010c0020t0001g0020a0010c0020t0001g0063a0012c0019t0001g0072others(3): Show | 7 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2571+1016_2571+103 others(19): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935267 | ||||||
chr1:177935293
|
T | C | 183 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(180): Show | 221 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.2571+1005A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935293 | ||||||
chr1:177935326
|
A | G | 306 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(303): Show | 381 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(378): Show |
intron_variant | MODIFIER | c.2571+972T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935326 | ||||||
chr1:177935360
|
T | C | 92 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(89): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2571+938A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935360 | ||||||
chr1:177935545
|
G | T | 40 | a0004c0002t0001g0221a0004c0002t0004g0003a0004c0002t0004g0027others(37): Show | 53 | HG00408.hp2 HG00621.hp1 HG01361.hp1 others(50): Show |
intron_variant | MODIFIER | c.2571+753C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935545 | ||||||
chr1:177935560
|
A | G | 1 | a0001c0006t0018g0189 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2571+738T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935560 | ||||||
chr1:177935616
|
T | C | 137 | a0001c0004t0001g0280a0001c0004t0004g0024a0001c0004t0004g0025others(134): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2571+682A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935616 | ||||||
chr1:177935662
|
GA | G | 94 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(91): Show | 109 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.2571+635delT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935662 | ||||||
chr1:177935781
|
T | C | 25 | a0001c0004t0001g0280a0001c0005t0001g0022a0001c0005t0001g0107others(22): Show | 31 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.2571+517A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935781 | ||||||
chr1:177935794
|
T | G | 11 | a0003c0008t0003g0058a0003c0008t0003g0098a0003c0008t0003g0099others(8): Show | 15 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2571+504A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935794 | ||||||
chr1:177935817
|
G | A | 45 | a0004c0002t0001g0128a0004c0002t0001g0221a0004c0002t0004g0003others(42): Show | 60 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.2571+481C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935817 | ||||||
chr1:177935836
|
T | C | 44 | a0004c0002t0001g0128a0004c0002t0001g0221a0004c0002t0004g0003others(41): Show | 58 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.2571+462A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935836 | ||||||
chr1:177935998
|
C | T | 1 | a0037c0056t0016g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2571+300G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177935998 | ||||||
chr1:177936039
|
T | C | 138 | a0001c0004t0001g0280a0001c0004t0004g0024a0001c0004t0004g0025others(135): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.2571+259A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177936039 | ||||||
chr1:177936055
|
G | A | 3 | a0001c0006t0007g0253a0005c0016t0002g0246a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2571+243C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177936055 | ||||||
chr1:177936131
|
C | T | 3 | a0001c0006t0001g0097a0021c0023t0001g0303a0021c0023t0001g0304 | 3 | NA18946.hp2 NA19067.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2571+167G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177936131 | ||||||
chr1:177936135
|
C | T | 10 | a0004c0010t0002g0298a0009c0015t0002g0039a0009c0015t0002g0215others(7): Show | 11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2571+163G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 20/25 | chr1 | 177936135 | ||||||
chr1:177936588
|
C | T | 1 | a0002c0001t0002g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2504-223G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177936588 | ||||||
chr1:177936752
|
C | T | 2 | a0018c0028t0005g0021a0027c0042t0005g0092 | 3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2504-387G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177936752 | ||||||
chr1:177936867
|
G | A | 1 | a0022c0032t0003g0286 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2503+347C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177936867 | ||||||
chr1:177936919
|
T | G | 218 | a0001c0004t0001g0280a0001c0004t0004g0024a0001c0004t0004g0025others(215): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.2503+295A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177936919 | ||||||
chr1:177936930
|
A | C | 2 | a0012c0019t0001g0072a0029c0040t0001g0095 | 2 | HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2503+284T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177936930 | ||||||
chr1:177937157
|
C | T | 68 | a0002c0001t0002g0001a0002c0001t0002g0004a0002c0001t0002g0005others(65): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2503+57G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177937157 | ||||||
chr1:177937201
|
G | A | 1 | a0001c0052t0012g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2503+13C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 19/25 | chr1 | 177937201 | ||||||
chr1:177937522
|
G | A | 75 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(72): Show | 86 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.2204-9C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177937522 | ||||||
chr1:177937624
|
A | G | 1 | a0001c0006t0001g0244 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2204-111T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177937624 | ||||||
chr1:177937654
|
T | C | 1 | a0003c0003t0003g0079 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2204-141A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177937654 | ||||||
chr1:177937706
|
T | G | 13 | a0004c0002t0008g0031a0004c0010t0002g0298a0004c0067t0008g0213others(10): Show | 15 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.2204-193A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177937706 | ||||||
chr1:177937998
|
A | T | 1 | a0002c0001t0002g0144 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2204-485T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177937998 | ||||||
chr1:177938118
|
A | G | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2204-605T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938118 | ||||||
chr1:177938298
|
G | A | 6 | a0001c0006t0007g0253a0004c0027t0006g0050a0005c0016t0002g0246others(3): Show | 7 | HG01074.hp1 HG01109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2204-785C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938298 | ||||||
chr1:177938301
|
AAGATCTT others(9): Show |
A | 102 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(99): Show | 123 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.2204-804_2204-789d others(18): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938301 | ||||||
chr1:177938328
|
T | C | 3 | a0001c0006t0007g0253a0005c0016t0002g0246a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2204-815A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938328 | ||||||
chr1:177938328
|
T | G | 1 | a0001c0006t0001g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2204-815A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938328 | ||||||
chr1:177938376
|
A | G | 102 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(99): Show | 123 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.2204-863T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938376 | ||||||
chr1:177938769
|
A | G | 1 | a0003c0003t0003g0204 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2203+933T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938769 | ||||||
chr1:177938838
|
G | A | 62 | a0001c0006t0007g0253a0004c0002t0001g0128a0004c0002t0001g0221others(59): Show | 78 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.2203+864C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938838 | ||||||
chr1:177938893
|
G | A | 1 | a0004c0002t0004g0160 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2203+809C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938893 | ||||||
chr1:177938963
|
G | A | 1 | a0001c0007t0001g0044 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2203+739C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938963 | ||||||
chr1:177938966
|
A | T | 1 | a0002c0001t0002g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2203+736T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177938966 | ||||||
chr1:177939012
|
C | T | 10 | a0004c0010t0002g0298a0009c0015t0002g0039a0009c0015t0002g0215others(7): Show | 11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2203+690G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939012 | ||||||
chr1:177939186
|
A | G | 62 | a0001c0006t0007g0253a0004c0002t0001g0128a0004c0002t0001g0221others(59): Show | 78 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.2203+516T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939186 | ||||||
chr1:177939187
|
C | G | 316 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(313): Show | 392 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(389): Show |
intron_variant | MODIFIER | c.2203+515G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939187 | ||||||
chr1:177939234
|
C | T | 5 | a0001c0006t0007g0253a0005c0016t0002g0246a0018c0028t0005g0021others(2): Show | 6 | HG01074.hp1 HG01109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2203+468G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939234 | ||||||
chr1:177939347
|
T | C | 44 | a0004c0002t0001g0128a0004c0002t0001g0221a0004c0002t0004g0003others(41): Show | 58 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.2203+355A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939347 | ||||||
chr1:177939426
|
T | C | 1 | a0001c0006t0001g0179 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2203+276A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939426 | ||||||
chr1:177939619
|
A | G | 1 | a0001c0007t0006g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2203+83T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939619 | ||||||
chr1:177939645
|
G | A | 2 | a0004c0027t0019g0327a0020c0068t0002g0088 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2203+57C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939645 | ||||||
chr1:177939672
|
T | C | 6 | a0001c0006t0007g0253a0004c0027t0006g0050a0005c0016t0002g0246others(3): Show | 7 | HG01074.hp1 HG01109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2203+30A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 18/25 | chr1 | 177939672 | ||||||
chr1:177939835
|
G | A | 1 | a0003c0003t0003g0292 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2128-58C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177939835 | ||||||
chr1:177939914
|
A | G | 2 | a0001c0036t0001g0121a0001c0036t0001g0122 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2128-137T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177939914 | ||||||
chr1:177939931
|
C | T | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2128-154G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177939931 | ||||||
chr1:177939991
|
C | T | 10 | a0004c0010t0002g0298a0009c0015t0002g0039a0009c0015t0002g0215others(7): Show | 11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2128-214G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177939991 | ||||||
chr1:177940059
|
A | G | 3 | a0001c0021t0001g0326a0001c0036t0001g0121a0001c0036t0001g0122 | 3 | HG02976.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2128-282T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940059 | ||||||
chr1:177940214
|
G | A | 4 | a0001c0063t0001g0132a0005c0016t0005g0138a0005c0054t0005g0124others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2127+396C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940214 | ||||||
chr1:177940400
|
C | T | 1 | a0001c0007t0001g0193 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2127+210G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940400 | ||||||
chr1:177940451
|
G | A | 1 | a0005c0011t0002g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2127+159C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940451 | ||||||
chr1:177940504
|
G | A | 1 | a0002c0001t0002g0315 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2127+106C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940504 | ||||||
chr1:177940512
|
G | T | 1 | a0028c0043t0003g0151 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2127+98C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940512 | ||||||
chr1:177940524
|
T | G | 10 | a0004c0010t0002g0298a0009c0015t0002g0039a0009c0015t0002g0215others(7): Show | 11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2127+86A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940524 | ||||||
chr1:177940543
|
T | C | 10 | a0004c0010t0002g0298a0009c0015t0002g0039a0009c0015t0002g0215others(7): Show | 11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2127+67A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940543 | ||||||
chr1:177940585
|
A | G | 1 | a0024c0038t0001g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2127+25T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940585 | ||||||
chr1:177940586
|
C | T | 1 | a0001c0006t0007g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2127+24G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 17/25 | chr1 | 177940586 | ||||||
chr1:177940772
|
G | C | 1 | a0007c0014t0002g0172 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2023-58C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177940772 | ||||||
chr1:177941101
|
G | A | 41 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(38): Show | 46 | HG00609.hp1 HG00621.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.2023-387C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941101 | ||||||
chr1:177941601
|
C | T | 1 | a0002c0001t0002g0005 | 4 | HG02258.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2022+299G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941601 | ||||||
chr1:177941667
|
A | G | 13 | a0004c0002t0008g0031a0004c0010t0002g0298a0004c0067t0008g0213others(10): Show | 15 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.2022+233T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941667 | ||||||
chr1:177941748
|
T | C | 1 | a0001c0004t0001g0259 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2022+152A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941748 | ||||||
chr1:177941761
|
A | G | 50 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(47): Show | 56 | HG00609.hp1 HG00621.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.2022+139T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941761 | ||||||
chr1:177941857
|
A | T | 1 | a0001c0052t0012g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2022+43T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 16/25 | chr1 | 177941857 | ||||||
chr1:177942378
|
G | A | 1 | a0002c0001t0002g0029 | 2 | HG00140.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1882-338C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942378 | ||||||
chr1:177942604
|
G | A | 1 | a0022c0032t0003g0134 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1882-564C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942604 | ||||||
chr1:177942653
|
G | A | 1 | a0002c0001t0002g0146 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1882-613C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942653 | ||||||
chr1:177942787
|
G | A | 6 | a0004c0002t0004g0166a0004c0002t0004g0168a0004c0002t0004g0169others(3): Show | 6 | HG01361.hp2 HG01496.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1882-747C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942787 | ||||||
chr1:177942836
|
G | A | 1 | a0004c0027t0006g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1882-796C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942836 | ||||||
chr1:177942846
|
T | A | 1 | a0001c0021t0001g0279 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1882-806A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177942846 | ||||||
chr1:177943071
|
C | T | 1 | a0004c0027t0006g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1882-1031G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943071 | ||||||
chr1:177943072
|
G | A | 54 | a0004c0002t0001g0128a0004c0002t0001g0221a0004c0002t0004g0003others(51): Show | 69 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1882-1032C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943072 | ||||||
chr1:177943112
|
C | T | 1 | a0003c0003t0013g0211 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1882-1072G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943112 | ||||||
chr1:177943113
|
G | A | 10 | a0004c0010t0002g0298a0009c0015t0002g0039a0009c0015t0002g0215others(7): Show | 11 | HG00423.hp2 HG00609.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1882-1073C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943113 | ||||||
chr1:177943129
|
T | C | 3 | a0001c0021t0001g0326a0001c0036t0001g0121a0001c0036t0001g0122 | 3 | HG02976.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1882-1089A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943129 | ||||||
chr1:177943194
|
A | G | 44 | a0004c0002t0001g0128a0004c0002t0001g0221a0004c0002t0004g0003others(41): Show | 58 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1882-1154T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943194 | ||||||
chr1:177943283
|
A | T | 68 | a0001c0007t0007g0307a0002c0001t0002g0001a0002c0001t0002g0004others(65): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1882-1243T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943283 | ||||||
chr1:177943525
|
G | A | 1 | a0002c0001t0002g0148 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1881+1036C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943525 | ||||||
chr1:177943650
|
T | G | 16 | a0001c0006t0007g0253a0001c0063t0001g0132a0004c0027t0006g0050others(13): Show | 17 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1881+911A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943650 | ||||||
chr1:177943660
|
A | G | 1 | a0003c0003t0003g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1881+901T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943660 | ||||||
chr1:177943680
|
T | C | 3 | a0001c0021t0001g0326a0001c0036t0001g0121a0001c0036t0001g0122 | 3 | HG02976.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1881+881A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943680 | ||||||
chr1:177943687
|
G | A | 41 | a0004c0002t0001g0128a0004c0002t0001g0221a0004c0002t0004g0003others(38): Show | 54 | HG00408.hp2 HG00621.hp1 HG01361.hp1 others(51): Show |
intron_variant | MODIFIER | c.1881+874C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943687 | ||||||
chr1:177943743
|
C | T | 1 | a0004c0027t0006g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1881+818G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943743 | ||||||
chr1:177943797
|
C | T | 43 | a0001c0004t0001g0280a0001c0005t0001g0022a0001c0005t0001g0107others(40): Show | 50 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1881+764G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177943797 | ||||||
chr1:177944013
|
A | G | 4 | a0003c0003t0003g0113a0003c0003t0003g0119a0003c0003t0003g0316others(1): Show | 4 | HG02165.hp1 NA18970.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1881+548T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944013 | ||||||
chr1:177944055
|
A | G | 46 | a0003c0018t0003g0232a0004c0002t0001g0128a0004c0002t0001g0221others(43): Show | 60 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1881+506T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944055 | ||||||
chr1:177944218
|
G | A | 1 | a0004c0002t0004g0164 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1881+343C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944218 | ||||||
chr1:177944225
|
C | G | 1 | a0003c0003t0003g0292 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1881+336G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944225 | ||||||
chr1:177944267
|
C | G | 103 | a0001c0004t0001g0280a0001c0005t0001g0022a0001c0005t0001g0107others(100): Show | 121 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1881+294G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944267 | ||||||
chr1:177944310
|
G | A | 1 | a0003c0003t0003g0296 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1881+251C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944310 | ||||||
chr1:177944384
|
T | C | 78 | a0001c0005t0001g0294a0001c0005t0002g0110a0001c0005t0002g0293others(75): Show | 91 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1881+177A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944384 | ||||||
chr1:177944440
|
T | C | 4 | a0001c0006t0001g0176a0001c0006t0001g0177a0001c0006t0001g0184others(1): Show | 4 | HG01123.hp2 HG03704.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1881+121A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944440 | ||||||
chr1:177944533
|
G | A | 4 | a0003c0003t0003g0287a0003c0003t0003g0295a0003c0008t0003g0102others(1): Show | 4 | NA18949.hp1 NA18971.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1881+28C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 15/25 | chr1 | 177944533 | ||||||
chr1:177944726
|
C | T | 1 | a0003c0008t0003g0320 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1776-60G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177944726 | ||||||
chr1:177944760
|
A | G | 1 | a0003c0003t0003g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1776-94T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177944760 | ||||||
chr1:177944797
|
G | A | 1 | a0004c0002t0004g0180 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1776-131C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177944797 | ||||||
chr1:177944845
|
T | C | 319 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(316): Show | 395 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(392): Show |
intron_variant | MODIFIER | c.1776-179A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177944845 | ||||||
chr1:177944917
|
G | A | 2 | a0005c0016t0003g0055a0005c0016t0003g0252 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1776-251C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177944917 | ||||||
chr1:177945051
|
C | A | 1 | a0004c0002t0004g0302 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1776-385G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945051 | ||||||
chr1:177945163
|
C | G | 3 | a0002c0001t0002g0013a0002c0001t0002g0125a0002c0001t0002g0126 | 5 | HG00735.hp2 HG01074.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1776-497G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945163 | ||||||
chr1:177945219
|
G | A | 1 | a0002c0001t0002g0220 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1776-553C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945219 | ||||||
chr1:177945246
|
C | G | 6 | a0010c0020t0001g0020a0010c0020t0001g0063a0012c0019t0001g0072others(3): Show | 7 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1776-580G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945246 | ||||||
chr1:177945312
|
T | G | 2 | a0005c0016t0003g0055a0005c0016t0003g0252 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1776-646A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945312 | ||||||
chr1:177945506
|
G | T | 1 | a0015c0022t0003g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1776-840C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945506 | ||||||
chr1:177945590
|
C | T | 23 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(20): Show | 30 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1775+830G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945590 | ||||||
chr1:177945593
|
A | G | 214 | a0001c0004t0001g0057a0001c0004t0001g0280a0001c0004t0004g0024others(211): Show | 255 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1775+827T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945593 | ||||||
chr1:177945598
|
A | T | 2 | a0018c0028t0005g0021a0027c0042t0005g0092 | 3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1775+822T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945598 | ||||||
chr1:177945611
|
C | T | 2 | a0018c0028t0005g0021a0027c0042t0005g0092 | 3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1775+809G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945611 | ||||||
chr1:177945630
|
C | T | 1 | a0001c0052t0012g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1775+790G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945630 | ||||||
chr1:177945636
|
A | G | 1 | a0001c0013t0001g0210 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1775+784T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945636 | ||||||
chr1:177945755
|
G | A | 2 | a0012c0019t0001g0072a0029c0040t0001g0095 | 2 | HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1775+665C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945755 | ||||||
chr1:177945792
|
G | A | 2 | a0001c0005t0001g0022a0001c0005t0001g0107 | 3 | NA18952.hp2 NA18989.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1775+628C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945792 | ||||||
chr1:177945868
|
C | T | 5 | a0003c0008t0003g0058a0003c0008t0003g0098a0003c0008t0003g0099others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1775+552G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945868 | ||||||
chr1:177945885
|
G | A | 63 | a0001c0004t0001g0105a0001c0005t0001g0016a0001c0007t0007g0307others(60): Show | 89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1775+535C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177945885 | ||||||
chr1:177946017
|
A | G | 2 | a0001c0036t0001g0121a0001c0036t0001g0122 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1775+403T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177946017 | ||||||
chr1:177946038
|
A | G | 6 | a0001c0063t0001g0132a0005c0054t0005g0124a0007c0014t0002g0186others(3): Show | 6 | HG01099.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1775+382T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177946038 | ||||||
chr1:177946339
|
A | C | 260 | a0001c0004t0001g0057a0001c0004t0001g0105a0001c0004t0001g0280others(257): Show | 332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1775+81T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177946339 | ||||||
chr1:177946363
|
G | A | 19 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(16): Show | 20 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1775+57C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 14/25 | chr1 | 177946363 | ||||||
chr1:177946562
|
C | T | 4 | a0007c0014t0002g0186a0011c0025t0005g0185a0011c0025t0005g0251others(1): Show | 4 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1664-31G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946562 | ||||||
chr1:177946563
|
G | A | 3 | a0002c0001t0002g0013a0002c0001t0002g0125a0002c0001t0002g0126 | 5 | HG00735.hp2 HG01074.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1664-32C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946563 | ||||||
chr1:177946643
|
A | G | 33 | a0001c0004t0001g0280a0001c0005t0001g0022a0001c0005t0001g0107others(30): Show | 39 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1664-112T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946643 | ||||||
chr1:177946648
|
A | T | 4 | a0001c0006t0007g0253a0005c0016t0002g0246a0005c0016t0003g0055others(1): Show | 4 | HG01074.hp1 HG01109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1664-117T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946648 | ||||||
chr1:177946679
|
C | T | 8 | a0003c0008t0003g0058a0003c0008t0003g0098a0003c0008t0003g0099others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1664-148G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946679 | ||||||
chr1:177946828
|
C | T | 1 | a0001c0052t0012g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1664-297G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946828 | ||||||
chr1:177946842
|
T | C | 1 | a0037c0056t0016g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1664-311A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946842 | ||||||
chr1:177946889
|
T | G | 6 | a0001c0005t0001g0083a0001c0005t0001g0202a0001c0005t0001g0291others(3): Show | 9 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1664-358A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177946889 | ||||||
chr1:177947046
|
A | G | 15 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(12): Show | 16 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1664-515T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947046 | ||||||
chr1:177947248
|
C | T | 7 | a0003c0008t0003g0065a0003c0008t0003g0066a0003c0008t0003g0067others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663+577G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947248 | ||||||
chr1:177947388
|
G | T | 2 | a0018c0028t0005g0021a0027c0042t0005g0092 | 3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1663+437C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947388 | ||||||
chr1:177947389
|
C | T | 2 | a0018c0028t0005g0021a0027c0042t0005g0092 | 3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1663+436G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947389 | ||||||
chr1:177947549
|
G | A | 1 | a0003c0026t0003g0178 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1663+276C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947549 | ||||||
chr1:177947692
|
C | T | 29 | a0001c0004t0001g0280a0001c0004t0004g0024a0001c0004t0004g0025others(26): Show | 40 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1663+133G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947692 | ||||||
chr1:177947693
|
G | C | 2 | a0004c0010t0004g0076a0034c0059t0003g0077 | 2 | NA18953.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1663+132C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947693 | ||||||
chr1:177947730
|
G | A | 16 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(13): Show | 20 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1663+95C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947730 | ||||||
chr1:177947736
|
C | T | 94 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(91): Show | 125 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1663+89G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947736 | ||||||
chr1:177947737
|
G | A | 17 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(14): Show | 21 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1663+88C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947737 | ||||||
chr1:177947754
|
A | G | 16 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(13): Show | 20 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1663+71T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947754 | ||||||
chr1:177947755
|
A | AAGGGACA others(18): Show |
241 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(238): Show | 298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.1663+69_1663+70ins others(25): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947755 | ||||||
chr1:177947755
|
A | G | 16 | a0001c0004t0004g0024a0001c0004t0004g0025a0001c0004t0004g0101others(13): Show | 20 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1663+70T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947755 | ||||||
chr1:177947771
|
A | AGGTGAGG others(19): Show |
1 | a0001c0006t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1663+53_1663+54ins others(26): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 13/25 | chr1 | 177947771 | ||||||
chr1:177948140
|
C | T | 2 | a0004c0027t0019g0327a0020c0068t0002g0088 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1546-198G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948140 | ||||||
chr1:177948281
|
C | T | 1 | a0001c0052t0012g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1546-339G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948281 | ||||||
chr1:177948321
|
G | A | 6 | a0001c0006t0007g0253a0005c0016t0002g0246a0005c0016t0003g0055others(3): Show | 7 | HG01074.hp1 HG01109.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546-379C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948321 | ||||||
chr1:177948344
|
G | A | 74 | a0001c0004t0001g0105a0001c0005t0001g0016a0001c0007t0007g0307others(71): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1546-402C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948344 | ||||||
chr1:177948364
|
G | A | 12 | a0004c0010t0002g0298a0007c0014t0002g0187a0009c0015t0002g0039others(9): Show | 13 | HG00423.hp2 HG00609.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1546-422C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948364 | ||||||
chr1:177948505
|
C | G | 1 | a0001c0004t0001g0280 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1546-563G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948505 | ||||||
chr1:177948709
|
C | T | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1546-767G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948709 | ||||||
chr1:177948922
|
T | TAC | 53 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(50): Show | 60 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1546-982_1546-981d others(4): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | ||||||
chr1:177948922
|
T | TACAC | 76 | a0001c0004t0001g0105a0001c0004t0001g0261a0001c0005t0001g0016others(73): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1546-984_1546-981d others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | ||||||
chr1:177948922
|
T | TACACAC | 8 | a0002c0001t0002g0008a0002c0001t0002g0041a0002c0001t0002g0149others(5): Show | 12 | HG00544.hp2 HG01192.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1546-986_1546-981d others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | ||||||
chr1:177948922
|
TAC | T | 14 | a0001c0052t0012g0052a0001c0063t0001g0132a0003c0008t0003g0058others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1546-982_1546-981d others(4): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | ||||||
chr1:177948922
|
TACACACA others(1): Show |
T | 29 | a0001c0005t0001g0022a0001c0005t0001g0107a0001c0005t0001g0198others(26): Show | 35 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1546-988_1546-981d others(10): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | ||||||
chr1:177948922
|
TACACACA others(3): Show |
T | 2 | a0001c0006t0001g0089a0001c0006t0001g0244 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1546-990_1546-981d others(12): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948922 | ||||||
chr1:177948992
|
G | A | 1 | a0002c0001t0002g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1546-1050C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177948992 | ||||||
chr1:177949030
|
A | G | 263 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(260): Show | 324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1546-1088T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949030 | ||||||
chr1:177949233
|
C | T | 1 | a0001c0007t0006g0018 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1546-1291G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949233 | ||||||
chr1:177949268
|
C | A | 1 | a0015c0022t0003g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1546-1326G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949268 | ||||||
chr1:177949291
|
A | G | 1 | a0020c0045t0002g0233 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1546-1349T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949291 | ||||||
chr1:177949364
|
G | A | 207 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(204): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1546-1422C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949364 | ||||||
chr1:177949383
|
A | AAC | 35 | a0001c0004t0004g0101a0001c0005t0001g0199a0001c0005t0001g0291others(32): Show | 40 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.1546-1443_1546-144 others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
A | AACAC | 19 | a0001c0006t0001g0244a0003c0003t0003g0047a0003c0003t0003g0109others(16): Show | 23 | HG00558.hp2 HG01243.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1546-1445_1546-144 others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
A | AACACAC | 5 | a0003c0008t0003g0243a0005c0016t0005g0138a0009c0015t0002g0216others(2): Show | 5 | HG01346.hp1 HG02145.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-1447_1546-144 others(10): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
A | AACACACA others(1): Show |
3 | a0003c0008t0003g0066a0003c0008t0003g0080a0003c0008t0003g0098 | 3 | HG01891.hp2 HG02630.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1546-1449_1546-144 others(12): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
A | AACACACA others(7): Show |
1 | a0001c0052t0012g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1546-1455_1546-144 others(18): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
AAC | A | 23 | a0001c0004t0001g0057a0001c0004t0001g0280a0001c0005t0004g0209others(20): Show | 26 | HG00639.hp1 HG01069.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1546-1443_1546-144 others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
AACAC | A | 12 | a0001c0005t0001g0310a0001c0005t0001g0312a0001c0005t0001g0313others(9): Show | 12 | HG00558.hp1 HG00733.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1546-1445_1546-144 others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
AACACAC | A | 30 | a0001c0004t0001g0045a0001c0004t0001g0259a0001c0005t0001g0022others(27): Show | 38 | HG00140.hp1 HG00280.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1546-1447_1546-144 others(10): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
AACACACA others(1): Show |
A | 8 | a0001c0004t0001g0139a0001c0004t0004g0104a0001c0006t0001g0174others(5): Show | 8 | HG01109.hp2 HG02486.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546-1449_1546-144 others(12): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
AACACACA others(3): Show |
A | 16 | a0001c0004t0001g0071a0001c0004t0001g0091a0001c0004t0001g0158others(13): Show | 16 | HG00621.hp2 HG01123.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1546-1451_1546-144 others(14): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
AACACACA others(5): Show |
A | 3 | a0005c0016t0002g0246a0031c0051t0007g0056a0037c0056t0016g0115 | 3 | HG01074.hp1 HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1546-1453_1546-144 others(16): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
AACACACA others(7): Show |
A | 14 | a0001c0004t0001g0256a0001c0004t0001g0258a0001c0004t0001g0262others(11): Show | 16 | HG02129.hp1 HG02165.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.1546-1455_1546-144 others(18): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
AACACACA others(9): Show |
A | 7 | a0002c0001t0002g0125a0002c0001t0002g0140a0002c0001t0002g0143others(4): Show | 8 | HG00735.hp2 HG01993.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546-1457_1546-144 others(20): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
AACACACA others(11): Show |
A | 67 | a0001c0004t0001g0105a0001c0005t0001g0016a0001c0061t0001g0289others(64): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1546-1459_1546-144 others(22): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949383
|
AACACACA others(13): Show |
A | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1546-1461_1546-144 others(24): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949383 | ||||||
chr1:177949417
|
CACACACA others(6): Show |
C | 1 | a0003c0003t0003g0238 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1546-1488_1546-147 others(17): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949417 | ||||||
chr1:177949429
|
C | A | 3 | a0003c0008t0003g0240a0003c0008t0003g0241a0003c0008t0003g0320 | 3 | HG02280.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1546-1487G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949429 | ||||||
chr1:177949429
|
C | CACACACA others(3): Show |
2 | a0003c0008t0003g0058a0003c0008t0003g0099 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1546-1488_1546-148 others(14): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949429 | ||||||
chr1:177949431
|
A | C | 2 | a0003c0003t0003g0237a0003c0003t0003g0282 | 2 | NA19079.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1546-1489T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949431 | ||||||
chr1:177949520
|
A | G | 9 | a0001c0007t0001g0044a0005c0011t0002g0010a0005c0011t0002g0011others(6): Show | 14 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1546-1578T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949520 | ||||||
chr1:177949524
|
T | TAGAG | 33 | a0001c0005t0001g0022a0001c0005t0001g0107a0001c0005t0001g0198others(30): Show | 39 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1546-1586_1546-158 others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949524 | ||||||
chr1:177949554
|
A | G | 3 | a0002c0001t0002g0154a0002c0001t0002g0265a0007c0014t0002g0086 | 3 | HG01168.hp2 HG03239.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1546-1612T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949554 | ||||||
chr1:177949632
|
T | C | 1 | a0001c0004t0001g0263 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1546-1690A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949632 | ||||||
chr1:177949686
|
A | G | 208 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(205): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1546-1744T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949686 | ||||||
chr1:177949709
|
C | T | 1 | a0001c0006t0001g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1546-1767G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949709 | ||||||
chr1:177949948
|
C | CA | 56 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(53): Show | 63 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1545+1965dupT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949948 | ||||||
chr1:177949948
|
C | CAA | 122 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(119): Show | 160 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1545+1964_1545+196 others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949948 | ||||||
chr1:177949948
|
C | CAAA | 33 | a0001c0005t0001g0022a0001c0005t0001g0107a0001c0006t0001g0006others(30): Show | 39 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1545+1963_1545+196 others(7): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949948 | ||||||
chr1:177949977
|
G | A | 1 | a0001c0004t0001g0264 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1545+1937C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949977 | ||||||
chr1:177949978
|
T | C | 1 | a0001c0004t0001g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1545+1936A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177949978 | ||||||
chr1:177950128
|
T | C | 1 | a0004c0002t0004g0161 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1545+1786A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950128 | ||||||
chr1:177950151
|
T | TA | 4 | a0001c0005t0001g0195a0004c0002t0001g0221a0004c0002t0004g0003others(1): Show | 8 | NA18942.hp1 NA18951.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1545+1762dupT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950151 | ||||||
chr1:177950151
|
TA | T | 190 | a0001c0004t0001g0057a0001c0004t0001g0105a0001c0004t0001g0280others(187): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1545+1762delT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950151 | ||||||
chr1:177950151
|
TAA | T | 27 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(24): Show | 29 | HG00609.hp2 HG00621.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1545+1761_1545+176 others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950151 | ||||||
chr1:177950163
|
A | T | 1 | a0003c0003t0003g0079 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1545+1751T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950163 | ||||||
chr1:177950166
|
A | G | 5 | a0001c0021t0001g0278a0001c0021t0001g0279a0001c0021t0001g0326others(2): Show | 5 | HG02818.hp2 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1545+1748T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950166 | ||||||
chr1:177950271
|
G | T | 2 | a0005c0016t0005g0138a0024c0038t0001g0254 | 2 | HG01346.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1545+1643C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950271 | ||||||
chr1:177950463
|
T | C | 17 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(14): Show | 19 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1545+1451A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950463 | ||||||
chr1:177950566
|
A | G | 1 | a0005c0016t0003g0252 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1545+1348T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950566 | ||||||
chr1:177950604
|
C | T | 1 | a0004c0002t0004g0037 | 2 | HG00408.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1545+1310G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950604 | ||||||
chr1:177950951
|
G | GGGAAGGA others(81): Show |
1 | a0001c0004t0001g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1545+962_1545+963i others(90): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177950951 | ||||||
chr1:177951131
|
G | A | 2 | a0018c0028t0005g0021a0027c0042t0005g0092 | 3 | HG02818.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1545+783C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951131 | ||||||
chr1:177951155
|
G | T | 2 | a0001c0063t0001g0132a0005c0054t0005g0124 | 2 | HG02055.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1545+759C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951155 | ||||||
chr1:177951256
|
A | C | 14 | a0001c0004t0001g0256a0004c0002t0004g0161a0004c0010t0002g0298others(11): Show | 15 | HG00423.hp2 HG00609.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1545+658T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951256 | ||||||
chr1:177951351
|
T | C | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1545+563A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951351 | ||||||
chr1:177951570
|
G | A | 1 | a0024c0038t0001g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1545+344C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951570 | ||||||
chr1:177951619
|
G | A | 115 | a0001c0004t0001g0057a0001c0004t0001g0105a0001c0004t0001g0280others(112): Show | 133 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1545+295C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951619 | ||||||
chr1:177951759
|
G | A | 1 | a0001c0052t0012g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1545+155C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 12/25 | chr1 | 177951759 | ||||||
chr1:177952018
|
C | T | 1 | a0002c0001t0002g0224 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1464-23G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952018 | ||||||
chr1:177952057
|
C | T | 1 | a0003c0003t0003g0084 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1464-62G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952057 | ||||||
chr1:177952187
|
C | T | 1 | a0004c0002t0001g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1464-192G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952187 | ||||||
chr1:177952299
|
T | A | 266 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(263): Show | 323 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1464-304A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952299 | ||||||
chr1:177952400
|
C | A | 2 | a0002c0001t0002g0005a0029c0040t0001g0095 | 5 | HG02258.hp1 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1464-405G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952400 | ||||||
chr1:177952413
|
C | T | 1 | a0005c0011t0002g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1464-418G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952413 | ||||||
chr1:177952453
|
C | A | 1 | a0005c0011t0002g0010 | 3 | HG02257.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1464-458G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952453 | ||||||
chr1:177952490
|
C | T | 3 | a0005c0016t0002g0246a0005c0016t0003g0055a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1464-495G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952490 | ||||||
chr1:177952624
|
G | A | 1 | a0002c0001t0002g0140 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1464-629C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952624 | ||||||
chr1:177952911
|
T | A | 1 | a0024c0038t0001g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1464-916A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952911 | ||||||
chr1:177952912
|
C | T | 4 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062others(1): Show | 4 | HG01346.hp1 HG01884.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-917G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177952912 | ||||||
chr1:177953003
|
A | AT | 35 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0025others(32): Show | 41 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1464-1009dupA | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953003 | ||||||
chr1:177953003
|
A | ATT | 123 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(120): Show | 154 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.1464-1010_1464-100 others(6): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953003 | ||||||
chr1:177953003
|
A | ATTT | 7 | a0001c0052t0012g0052a0003c0003t0003g0237a0003c0003t0003g0238others(4): Show | 8 | HG02717.hp1 HG02818.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1464-1011_1464-100 others(7): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953003 | ||||||
chr1:177953003
|
AT | A | 66 | a0001c0006t0001g0006a0001c0006t0001g0007a0001c0006t0001g0053others(63): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1464-1009delA | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953003 | ||||||
chr1:177953108
|
C | T | 2 | a0001c0006t0007g0253a0005c0016t0003g0252 | 2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1464-1113G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953108 | ||||||
chr1:177953163
|
A | G | 232 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(229): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1463+1116T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953163 | ||||||
chr1:177953220
|
G | C | 1 | a0037c0056t0016g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1463+1059C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953220 | ||||||
chr1:177953336
|
C | A | 125 | a0001c0005t0001g0016a0001c0005t0001g0022a0001c0005t0001g0043others(122): Show | 155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1463+943G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953336 | ||||||
chr1:177953482
|
A | G | 125 | a0001c0005t0001g0016a0001c0005t0001g0022a0001c0005t0001g0043others(122): Show | 155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1463+797T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953482 | ||||||
chr1:177953562
|
A | C | 14 | a0004c0010t0002g0298a0007c0014t0002g0187a0007c0034t0002g0133others(11): Show | 15 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.1463+717T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953562 | ||||||
chr1:177953669
|
AT | A | 7 | a0001c0007t0001g0044a0005c0011t0002g0010a0005c0011t0002g0011others(4): Show | 12 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1463+609delA | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953669 | ||||||
chr1:177953718
|
T | G | 3 | a0001c0006t0001g0179a0001c0013t0001g0023a0001c0013t0001g0028 | 5 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463+561A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953718 | ||||||
chr1:177953838
|
G | A | 3 | a0005c0016t0002g0246a0005c0016t0003g0055a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1463+441C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953838 | ||||||
chr1:177953985
|
A | G | 1 | a0003c0018t0003g0232 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1463+294T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177953985 | ||||||
chr1:177954110
|
G | A | 1 | a0004c0027t0006g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1463+169C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177954110 | ||||||
chr1:177954189
|
G | A | 14 | a0004c0010t0002g0298a0007c0014t0002g0187a0007c0034t0002g0133others(11): Show | 15 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.1463+90C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 11/25 | chr1 | 177954189 | ||||||
chr1:177954396
|
A | G | 1 | a0001c0007t0001g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1366-20T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177954396 | ||||||
chr1:177954522
|
G | A | 2 | a0001c0006t0001g0089a0001c0006t0001g0244 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1366-146C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177954522 | ||||||
chr1:177954934
|
A | G | 1 | a0024c0038t0001g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1366-558T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177954934 | ||||||
chr1:177955011
|
C | A | 36 | a0001c0006t0001g0006a0001c0006t0001g0007a0001c0006t0001g0053others(33): Show | 44 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.1366-635G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955011 | ||||||
chr1:177955137
|
T | TAAAAAAT others(273): Show |
1 | a0024c0038t0001g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1366-762_1366-761i others(282): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955137 | ||||||
chr1:177955137
|
T | TAAAAAAT others(293): Show |
2 | a0001c0017t0001g0061a0019c0024t0010g0062 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1366-762_1366-761i others(302): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955137 | ||||||
chr1:177955137
|
T | TAAAAAAT others(294): Show |
1 | a0019c0024t0010g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1366-762_1366-761i others(303): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955137 | ||||||
chr1:177955146
|
T | C | 1 | a0001c0005t0001g0310 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1366-770A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955146 | ||||||
chr1:177955219
|
G | A | 53 | a0001c0006t0001g0006a0001c0006t0001g0053a0001c0006t0001g0070others(50): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1366-843C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955219 | ||||||
chr1:177955223
|
C | A | 7 | a0001c0063t0001g0132a0005c0016t0002g0246a0005c0016t0003g0055others(4): Show | 7 | HG01074.hp1 HG01109.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366-847G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955223 | ||||||
chr1:177955223
|
C | T | 1 | a0001c0006t0001g0173 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1366-847G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955223 | ||||||
chr1:177955339
|
A | T | 1 | a0004c0027t0006g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1366-963T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955339 | ||||||
chr1:177955394
|
T | C | 118 | a0001c0005t0001g0016a0001c0005t0001g0022a0001c0005t0001g0043others(115): Show | 148 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1366-1018A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955394 | ||||||
chr1:177955424
|
TGCAACCT others(11): Show |
T | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1066_1366-104 others(22): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955424 | ||||||
chr1:177955443
|
G | A | 53 | a0001c0006t0001g0006a0001c0006t0001g0053a0001c0006t0001g0070others(50): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1366-1067C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955443 | ||||||
chr1:177955444
|
T | G | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1068A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955444 | ||||||
chr1:177955446
|
T | G | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1070A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955446 | ||||||
chr1:177955448
|
A | G | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1072T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955448 | ||||||
chr1:177955449
|
G | C | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1073C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955449 | ||||||
chr1:177955454
|
T | G | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1078A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955454 | ||||||
chr1:177955455
|
C | A | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1079G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955455 | ||||||
chr1:177955463
|
T | A | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1087A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955463 | ||||||
chr1:177955465
|
A | T | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1089T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955465 | ||||||
chr1:177955468
|
C | A | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1092G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955468 | ||||||
chr1:177955469
|
T | C | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1093A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955469 | ||||||
chr1:177955470
|
C | T | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1094G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955470 | ||||||
chr1:177955478
|
G | A | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1366-1102C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955478 | ||||||
chr1:177955478
|
G | C | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1102C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955478 | ||||||
chr1:177955486
|
T | A | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1110A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955486 | ||||||
chr1:177955492
|
C | A | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1116G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955492 | ||||||
chr1:177955497
|
C | CTCTCCAA others(8): Show |
1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1122_1366-112 others(19): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955497 | ||||||
chr1:177955500
|
T | C | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1124A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955500 | ||||||
chr1:177955504
|
G | T | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1128C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955504 | ||||||
chr1:177955506
|
C | A | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1130G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955506 | ||||||
chr1:177955508
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1132C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955508 | ||||||
chr1:177955517
|
T | A | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1141A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955517 | ||||||
chr1:177955518
|
T | A | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1142A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955518 | ||||||
chr1:177955519
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1143C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955519 | ||||||
chr1:177955521
|
A | T | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1145T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955521 | ||||||
chr1:177955533
|
G | T | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1157C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955533 | ||||||
chr1:177955536
|
G | T | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1160C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955536 | ||||||
chr1:177955542
|
T | G | 1 | a0001c0004t0001g0071 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1366-1166A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955542 | ||||||
chr1:177955798
|
C | A | 1 | a0037c0056t0016g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1366-1422G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177955798 | ||||||
chr1:177956033
|
A | C | 1 | a0002c0001t0002g0042 | 2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1366-1657T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956033 | ||||||
chr1:177956128
|
T | A | 46 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(43): Show | 53 | HG00140.hp1 HG00280.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1366-1752A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956128 | ||||||
chr1:177956166
|
A | C | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1366-1790T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956166 | ||||||
chr1:177956225
|
A | C | 1 | a0024c0038t0001g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1366-1849T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956225 | ||||||
chr1:177956260
|
C | A | 36 | a0001c0006t0001g0006a0001c0006t0001g0053a0001c0006t0001g0070others(33): Show | 41 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1365+1872G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956260 | ||||||
chr1:177956389
|
T | A | 26 | a0001c0006t0001g0006a0001c0006t0001g0053a0001c0006t0001g0070others(23): Show | 31 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1365+1743A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956389 | ||||||
chr1:177956542
|
A | G | 18 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(15): Show | 20 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1365+1590T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956542 | ||||||
chr1:177956593
|
TTATC | T | 28 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(25): Show | 34 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1365+1535_1365+153 others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956593 | ||||||
chr1:177956596
|
T | C | 1 | a0024c0038t0001g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1365+1536A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177956596 | ||||||
chr1:177957080
|
A | G | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1365+1052T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957080 | ||||||
chr1:177957117
|
C | G | 1 | a0001c0004t0001g0258 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1365+1015G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957117 | ||||||
chr1:177957123
|
A | G | 1 | a0006c0009t0004g0141 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1365+1009T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957123 | ||||||
chr1:177957231
|
T | A | 1 | a0005c0016t0005g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1365+901A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957231 | ||||||
chr1:177957234
|
A | G | 1 | a0037c0056t0016g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1365+898T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957234 | ||||||
chr1:177957322
|
T | TTGTATAA others(328): Show |
1 | a0001c0036t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1365+809_1365+810i others(337): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957322 | ||||||
chr1:177957376
|
T | C | 1 | a0003c0003t0013g0211 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1365+756A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957376 | ||||||
chr1:177957440
|
C | G | 2 | a0004c0002t0004g0155a0004c0002t0004g0302 | 2 | NA18612.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1365+692G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957440 | ||||||
chr1:177957614
|
T | C | 28 | a0001c0004t0001g0057a0003c0008t0003g0058a0003c0008t0003g0065others(25): Show | 29 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1365+518A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957614 | ||||||
chr1:177957854
|
T | C | 1 | a0002c0001t0002g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1365+278A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957854 | ||||||
chr1:177957934
|
G | A | 1 | a0011c0025t0005g0251 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1365+198C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177957934 | ||||||
chr1:177958053
|
A | G | 25 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(22): Show | 27 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1365+79T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 10/25 | chr1 | 177958053 | ||||||
chr1:177958519
|
C | A | 74 | a0001c0004t0001g0057a0001c0004t0001g0105a0001c0004t0001g0280others(71): Show | 87 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1135-157G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 9/25 | chr1 | 177958519 | ||||||
chr1:177958593
|
C | A | 2 | a0002c0001t0002g0301a0002c0001t0002g0311 | 2 | NA18974.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1135-231G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 9/25 | chr1 | 177958593 | ||||||
chr1:177958661
|
C | G | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1134+179G>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 9/25 | chr1 | 177958661 | ||||||
chr1:177958723
|
C | T | 2 | a0003c0003t0003g0282a0003c0003t0003g0283 | 2 | NA19065.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1134+117G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 9/25 | chr1 | 177958723 | ||||||
chr1:177958778
|
A | G | 1 | a0001c0005t0017g0135 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1134+62T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 9/25 | chr1 | 177958778 | ||||||
chr1:177959001
|
A | T | 1 | a0012c0019t0001g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.999-26T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959001 | ||||||
chr1:177959032
|
G | A | 1 | a0006c0009t0004g0314 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.999-57C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959032 | ||||||
chr1:177959088
|
A | C | 4 | a0005c0016t0002g0246a0005c0016t0003g0055a0031c0051t0007g0056others(1): Show | 4 | HG01074.hp1 HG01109.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-113T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959088 | ||||||
chr1:177959130
|
G | A | 2 | a0001c0006t0001g0053a0032c0046t0001g0170 | 2 | HG01192.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.999-155C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959130 | ||||||
chr1:177959435
|
G | T | 1 | a0001c0004t0001g0139 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.999-460C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959435 | ||||||
chr1:177959478
|
G | T | 24 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(21): Show | 26 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.999-503C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959478 | ||||||
chr1:177959826
|
C | A | 26 | a0001c0006t0001g0006a0001c0006t0001g0070a0001c0006t0001g0089others(23): Show | 29 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.998+516G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959826 | ||||||
chr1:177959904
|
T | A | 1 | a0004c0002t0004g0180 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.998+438A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959904 | ||||||
chr1:177959939
|
G | T | 1 | a0001c0004t0001g0280 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.998+403C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959939 | ||||||
chr1:177959953
|
C | T | 1 | a0024c0038t0001g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.998+389G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177959953 | ||||||
chr1:177960102
|
T | C | 1 | a0001c0052t0012g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.998+240A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177960102 | ||||||
chr1:177960128
|
C | T | 1 | a0003c0003t0003g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.998+214G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177960128 | ||||||
chr1:177960160
|
TG | T | 17 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(14): Show | 19 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.998+181delC | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177960160 | ||||||
chr1:177960244
|
C | T | 58 | a0001c0004t0001g0057a0001c0004t0001g0105a0001c0004t0001g0280others(55): Show | 70 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.998+98G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177960244 | ||||||
chr1:177960333
|
G | A | 1 | a0004c0002t0004g0037 | 2 | HG00408.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.998+9C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 8/25 | chr1 | 177960333 | ||||||
chr1:177960419
|
C | T | 159 | a0001c0005t0001g0016a0001c0005t0001g0022a0001c0005t0001g0043others(156): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.937-16G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960419 | ||||||
chr1:177960471
|
A | G | 3 | a0003c0008t0003g0065a0003c0008t0003g0066a0003c0008t0003g0067 | 3 | HG02559.hp2 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.937-68T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960471 | ||||||
chr1:177960493
|
G | A | 24 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(21): Show | 26 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.937-90C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960493 | ||||||
chr1:177960632
|
T | C | 11 | a0009c0015t0002g0039a0009c0015t0002g0215a0009c0015t0002g0216others(8): Show | 12 | HG00423.hp2 HG00609.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.936+159A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960632 | ||||||
chr1:177960701
|
C | T | 24 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(21): Show | 26 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.936+90G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960701 | ||||||
chr1:177960780
|
G | C | 6 | a0001c0021t0001g0278a0001c0021t0001g0279a0001c0021t0001g0326others(3): Show | 6 | HG02717.hp1 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+11C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 7/25 | chr1 | 177960780 | ||||||
chr1:177960961
|
T | C | 80 | a0001c0005t0001g0022a0001c0005t0001g0107a0001c0005t0001g0312others(77): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.788-22A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177960961 | ||||||
chr1:177961100
|
C | T | 1 | a0004c0010t0008g0284 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.788-161G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961100 | ||||||
chr1:177961143
|
G | A | 16 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(13): Show | 17 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.788-204C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961143 | ||||||
chr1:177961143
|
G | T | 1 | a0004c0027t0019g0327 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.788-204C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961143 | ||||||
chr1:177961182
|
C | T | 4 | a0004c0002t0001g0221a0004c0002t0004g0003a0004c0002t0004g0159others(1): Show | 8 | NA18942.hp1 NA18951.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.788-243G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961182 | ||||||
chr1:177961184
|
C | T | 78 | a0001c0005t0001g0022a0001c0005t0001g0107a0001c0005t0001g0312others(75): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.788-245G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961184 | ||||||
chr1:177961373
|
AG | A | 15 | a0004c0002t0004g0027a0004c0002t0004g0116a0004c0002t0004g0183others(12): Show | 17 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.787+216delC | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961373 | ||||||
chr1:177961507
|
G | A | 144 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(141): Show | 174 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.787+83C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 6/25 | chr1 | 177961507 | ||||||
chr1:177961759
|
C | T | 258 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(255): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.643-25G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177961759 | ||||||
chr1:177961794
|
G | A | 1 | a0005c0016t0005g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.643-60C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177961794 | ||||||
chr1:177961820
|
C | T | 3 | a0005c0016t0002g0246a0005c0016t0003g0055a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.643-86G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177961820 | ||||||
chr1:177961951
|
C | T | 147 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(144): Show | 180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.643-217G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177961951 | ||||||
chr1:177961987
|
G | A | 89 | a0001c0005t0001g0016a0001c0005t0001g0022a0001c0005t0001g0043others(86): Show | 109 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.643-253C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177961987 | ||||||
chr1:177962176
|
C | T | 1 | a0004c0010t0009g0196 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.643-442G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962176 | ||||||
chr1:177962177
|
G | T | 1 | a0003c0008t0003g0080 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.643-443C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962177 | ||||||
chr1:177962221
|
G | A | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.643-487C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962221 | ||||||
chr1:177962352
|
G | C | 5 | a0001c0021t0001g0278a0001c0021t0001g0279a0001c0021t0001g0326others(2): Show | 5 | HG02818.hp2 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-618C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962352 | ||||||
chr1:177962373
|
C | A | 150 | a0001c0004t0001g0057a0001c0004t0001g0105a0001c0004t0001g0280others(147): Show | 183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.643-639G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962373 | ||||||
chr1:177962397
|
C | A | 71 | a0001c0006t0001g0006a0001c0006t0001g0007a0001c0006t0001g0053others(68): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.643-663G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962397 | ||||||
chr1:177962546
|
T | C | 3 | a0005c0016t0002g0246a0005c0016t0003g0055a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.643-812A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962546 | ||||||
chr1:177962758
|
T | G | 1 | a0002c0001t0002g0140 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.643-1024A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962758 | ||||||
chr1:177962789
|
G | T | 4 | a0001c0004t0001g0057a0001c0017t0001g0061a0019c0024t0010g0054others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-1055C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962789 | ||||||
chr1:177962861
|
C | T | 16 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(13): Show | 18 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.643-1127G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962861 | ||||||
chr1:177962864
|
T | G | 4 | a0001c0004t0001g0057a0001c0017t0001g0061a0019c0024t0010g0054others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-1130A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962864 | ||||||
chr1:177962876
|
G | A | 4 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-1142C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962876 | ||||||
chr1:177962907
|
GACCAGCC others(489): Show |
G | 12 | a0001c0004t0001g0158a0002c0001t0002g0008a0002c0001t0002g0041others(9): Show | 16 | HG00597.hp2 HG01192.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.642+768_643-1174de others(1): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962907 | ||||||
chr1:177962965
|
G | A | 1 | a0001c0004t0001g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.642+1206C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962965 | ||||||
chr1:177962969
|
A | G | 261 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(258): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.642+1202T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177962969 | ||||||
chr1:177963167
|
T | C | 12 | a0004c0067t0008g0213a0009c0015t0002g0039a0009c0015t0002g0215others(9): Show | 13 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.642+1004A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963167 | ||||||
chr1:177963228
|
T | C | 146 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(143): Show | 179 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.642+943A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963228 | ||||||
chr1:177963249
|
G | T | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.642+922C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963249 | ||||||
chr1:177963276
|
G | A | 3 | a0001c0021t0001g0326a0001c0036t0001g0121a0001c0036t0001g0122 | 3 | HG02976.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+895C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963276 | ||||||
chr1:177963318
|
T | G | 3 | a0005c0016t0002g0246a0005c0016t0003g0055a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.642+853A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963318 | ||||||
chr1:177963327
|
G | A | 1 | a0001c0063t0001g0132 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.642+844C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963327 | ||||||
chr1:177963343
|
G | C | 46 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(43): Show | 58 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.642+828C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963343 | ||||||
chr1:177963464
|
A | G | 269 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(266): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.642+707T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963464 | ||||||
chr1:177963683
|
TA | T | 4 | a0001c0004t0001g0057a0001c0017t0001g0061a0019c0024t0010g0054others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+487delT | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963683 | ||||||
chr1:177963764
|
A | G | 3 | a0005c0016t0002g0246a0005c0016t0003g0055a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.642+407T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963764 | ||||||
chr1:177963791
|
G | A | 3 | a0005c0016t0002g0246a0005c0016t0003g0055a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.642+380C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963791 | ||||||
chr1:177963925
|
C | T | 1 | a0004c0027t0006g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.642+246G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177963925 | ||||||
chr1:177964007
|
A | G | 3 | a0001c0017t0001g0061a0019c0024t0010g0054a0019c0024t0010g0062 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.642+164T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177964007 | ||||||
chr1:177964145
|
C | T | 1 | a0003c0003t0003g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.642+26G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177964145 | ||||||
chr1:177964155
|
C | A | 1 | a0001c0006t0001g0184 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.642+16G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177964155 | ||||||
chr1:177964155
|
C | T | 1 | a0004c0010t0008g0284 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.642+16G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 5/25 | chr1 | 177964155 | ||||||
chr1:177964308
|
G | A | 143 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(140): Show | 176 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.534-29C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964308 | ||||||
chr1:177964348
|
C | T | 1 | a0037c0056t0016g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.534-69G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964348 | ||||||
chr1:177964370
|
C | T | 85 | a0001c0005t0001g0016a0001c0005t0001g0022a0001c0005t0001g0043others(82): Show | 105 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.534-91G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964370 | ||||||
chr1:177964402
|
T | C | 4 | a0001c0004t0001g0057a0001c0017t0001g0061a0019c0024t0010g0054others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-123A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964402 | ||||||
chr1:177964538
|
A | G | 2 | a0003c0003t0003g0282a0003c0003t0003g0283 | 2 | NA19065.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.534-259T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964538 | ||||||
chr1:177964548
|
G | A | 4 | a0007c0014t0002g0186a0011c0025t0005g0185a0011c0025t0005g0251others(1): Show | 4 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-269C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964548 | ||||||
chr1:177964670
|
A | T | 4 | a0001c0004t0001g0057a0001c0017t0001g0061a0019c0024t0010g0054others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+377T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964670 | ||||||
chr1:177964686
|
A | G | 1 | a0001c0004t0001g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.533+361T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964686 | ||||||
chr1:177964694
|
A | C | 180 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(177): Show | 215 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.533+353T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964694 | ||||||
chr1:177964697
|
G | A | 1 | a0008c0041t0007g0156 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.533+350C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964697 | ||||||
chr1:177964779
|
C | T | 1 | a0001c0005t0001g0022 | 2 | NA18952.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.533+268G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964779 | ||||||
chr1:177964809
|
C | T | 1 | a0037c0056t0016g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.533+238G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964809 | ||||||
chr1:177964892
|
A | C | 2 | a0001c0052t0012g0052a0039c0037t0003g0239 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.533+155T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964892 | ||||||
chr1:177964909
|
T | C | 149 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(146): Show | 182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.533+138A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964909 | ||||||
chr1:177964987
|
G | T | 16 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(13): Show | 18 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.533+60C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 4/25 | chr1 | 177964987 | ||||||
chr1:177965216
|
G | T | 83 | a0001c0005t0001g0016a0001c0005t0001g0022a0001c0005t0001g0043others(80): Show | 103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.413-49C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965216 | ||||||
chr1:177965324
|
A | G | 2 | a0001c0007t0001g0044a0005c0011t0002g0010 | 5 | HG02257.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-157T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965324 | ||||||
chr1:177965332
|
T | C | 146 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(143): Show | 179 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.413-165A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965332 | ||||||
chr1:177965400
|
G | GGTGTGTG others(1): Show |
14 | a0001c0063t0001g0132a0004c0067t0008g0213a0009c0015t0002g0039others(11): Show | 15 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.413-241_413-234dup others(8): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | ||||||
chr1:177965400
|
G | GGTGTGTG others(3): Show |
82 | a0001c0005t0001g0016a0001c0005t0001g0022a0001c0005t0001g0043others(79): Show | 102 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.413-243_413-234dup others(10): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | ||||||
chr1:177965400
|
G | GGTGTGTG others(5): Show |
38 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(35): Show | 45 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.413-245_413-234dup others(12): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | ||||||
chr1:177965400
|
G | GGTGTGTG others(7): Show |
13 | a0001c0007t0001g0044a0003c0008t0003g0065a0003c0008t0003g0066others(10): Show | 18 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.413-247_413-234dup others(14): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | ||||||
chr1:177965400
|
G | GGTGTGTG others(9): Show |
1 | a0012c0019t0006g0048 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.413-249_413-234dup others(16): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | ||||||
chr1:177965400
|
G | GGTGTGTG others(13): Show |
6 | a0001c0052t0012g0052a0003c0008t0003g0240a0003c0008t0003g0241others(3): Show | 6 | HG01243.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-234_413-233ins others(20): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | ||||||
chr1:177965400
|
G | GGTGTGTG others(15): Show |
16 | a0001c0004t0001g0045a0001c0004t0001g0071a0001c0004t0001g0091others(13): Show | 17 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.413-234_413-233ins others(22): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | ||||||
chr1:177965400
|
G | GGTGTGTG others(17): Show |
7 | a0001c0004t0001g0256a0001c0004t0001g0257a0001c0017t0001g0061others(4): Show | 8 | HG01884.hp1 HG02258.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.413-234_413-233ins others(24): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | ||||||
chr1:177965400
|
G | GGTGTGTG others(19): Show |
1 | a0001c0004t0001g0255 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.413-234_413-233ins others(26): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | ||||||
chr1:177965400
|
G | GGTGTGTG others(21): Show |
1 | a0001c0004t0001g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.413-234_413-233ins others(28): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965400 | ||||||
chr1:177965456
|
T | C | 149 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(146): Show | 182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.413-289A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965456 | ||||||
chr1:177965472
|
C | T | 3 | a0005c0016t0002g0246a0005c0016t0003g0055a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.413-305G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965472 | ||||||
chr1:177965477
|
T | C | 5 | a0007c0014t0002g0186a0011c0025t0005g0185a0011c0025t0005g0251others(2): Show | 5 | HG01099.hp1 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-310A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965477 | ||||||
chr1:177965491
|
T | C | 1 | a0031c0051t0007g0056 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.413-324A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965491 | ||||||
chr1:177965611
|
A | G | 14 | a0001c0021t0001g0278a0001c0021t0001g0279a0001c0021t0001g0326others(11): Show | 14 | HG01243.hp2 HG02145.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.412+282T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965611 | ||||||
chr1:177965832
|
G | C | 4 | a0007c0014t0002g0186a0011c0025t0005g0185a0011c0025t0005g0251others(1): Show | 4 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+61C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 3/25 | chr1 | 177965832 | ||||||
chr1:177966017
|
C | A | 4 | a0007c0014t0002g0186a0011c0025t0005g0185a0011c0025t0005g0251others(1): Show | 4 | HG01099.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-12G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966017 | ||||||
chr1:177966027
|
T | A | 1 | a0003c0026t0003g0235 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.300-22A>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966027 | ||||||
chr1:177966031
|
C | T | 1 | a0001c0063t0001g0132 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.300-26G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966031 | ||||||
chr1:177966068
|
A | G | 146 | a0001c0004t0001g0057a0001c0004t0001g0105a0001c0004t0001g0280others(143): Show | 179 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.300-63T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966068 | ||||||
chr1:177966140
|
A | G | 268 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(265): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.300-135T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966140 | ||||||
chr1:177966209
|
T | C | 5 | a0001c0006t0001g0190a0001c0006t0018g0189a0001c0048t0001g0129others(2): Show | 5 | HG00140.hp1 HG01070.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-204A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966209 | ||||||
chr1:177966295
|
C | A | 2 | a0003c0003t0003g0084a0003c0003t0003g0085 | 2 | NA18959.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.300-290G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966295 | ||||||
chr1:177966308
|
C | T | 142 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(139): Show | 175 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.300-303G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966308 | ||||||
chr1:177966392
|
C | A | 1 | a0005c0016t0002g0246 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.300-387G>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966392 | ||||||
chr1:177966530
|
G | A | 45 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(42): Show | 57 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.300-525C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966530 | ||||||
chr1:177966572
|
ATT | A | 141 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(138): Show | 174 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.300-569_300-568del others(2): Show |
SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966572 | ||||||
chr1:177966678
|
G | A | 1 | a0001c0004t0001g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.300-673C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966678 | ||||||
chr1:177966795
|
G | A | 142 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(139): Show | 175 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.300-790C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966795 | ||||||
chr1:177966836
|
A | T | 1 | a0002c0001t0020g0328 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.300-831T>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966836 | ||||||
chr1:177966892
|
T | C | 145 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(142): Show | 178 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.299+791A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177966892 | ||||||
chr1:177967109
|
G | A | 2 | a0001c0021t0001g0278a0001c0021t0001g0279 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.299+574C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967109 | ||||||
chr1:177967268
|
G | A | 6 | a0003c0008t0003g0240a0003c0008t0003g0241a0005c0011t0002g0060others(3): Show | 6 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.299+415C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967268 | ||||||
chr1:177967346
|
A | C | 268 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(265): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.299+337T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967346 | ||||||
chr1:177967390
|
A | G | 30 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(27): Show | 36 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.299+293T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967390 | ||||||
chr1:177967401
|
T | G | 116 | a0001c0004t0001g0158a0001c0006t0001g0006a0001c0006t0001g0007others(113): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.299+282A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967401 | ||||||
chr1:177967464
|
T | G | 134 | a0001c0004t0001g0105a0001c0004t0001g0280a0001c0004t0004g0024others(131): Show | 161 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.299+219A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967464 | ||||||
chr1:177967556
|
C | T | 3 | a0005c0016t0002g0246a0005c0016t0003g0055a0031c0051t0007g0056 | 3 | HG01074.hp1 HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.299+127G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967556 | ||||||
chr1:177967671
|
C | T | 1 | a0005c0016t0005g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299+12G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 2/25 | chr1 | 177967671 | ||||||
chr1:177968143
|
A | C | 3 | a0001c0006t0001g0070a0004c0027t0019g0327a0020c0068t0002g0088 | 3 | HG02145.hp2 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-58-104T>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968143 | ||||||
chr1:177968163
|
T | C | 1 | a0003c0003t0003g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-58-124A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968163 | ||||||
chr1:177968241
|
C | T | 2 | a0001c0036t0001g0121a0001c0036t0001g0122 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-58-202G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968241 | ||||||
chr1:177968306
|
A | G | 169 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(166): Show | 215 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-58-267T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968306 | ||||||
chr1:177968396
|
C | T | 1 | a0001c0006t0001g0120 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-58-357G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968396 | ||||||
chr1:177968419
|
C | T | 1 | a0003c0003t0003g0119 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-58-380G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968419 | ||||||
chr1:177968430
|
T | C | 2 | a0001c0005t0001g0312a0001c0005t0001g0313 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-58-391A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968430 | ||||||
chr1:177968577
|
C | T | 1 | a0011c0025t0005g0251 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-58-538G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968577 | ||||||
chr1:177968585
|
G | A | 1 | a0002c0001t0002g0220 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-58-546C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968585 | ||||||
chr1:177968603
|
T | C | 169 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(166): Show | 212 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.-58-564A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968603 | ||||||
chr1:177968620
|
A | G | 176 | a0001c0004t0001g0045a0001c0004t0001g0057a0001c0004t0001g0071others(173): Show | 219 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(216): Show |
intron_variant | MODIFIER | c.-58-581T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968620 | ||||||
chr1:177968829
|
A | G | 33 | a0001c0004t0001g0057a0001c0006t0001g0089a0001c0006t0001g0244others(30): Show | 39 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-58-790T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968829 | ||||||
chr1:177968922
|
G | A | 19 | a0001c0005t0002g0236a0002c0001t0002g0008a0002c0001t0002g0040others(16): Show | 24 | HG00741.hp1 HG01192.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-58-883C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968922 | ||||||
chr1:177968995
|
C | T | 29 | a0001c0004t0001g0057a0001c0005t0001g0043a0001c0006t0001g0244others(26): Show | 37 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-59+889G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177968995 | ||||||
chr1:177969099
|
T | G | 3 | a0001c0006t0001g0053a0001c0052t0012g0052a0019c0024t0010g0054 | 3 | HG01192.hp1 HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-59+785A>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969099 | ||||||
chr1:177969108
|
T | C | 6 | a0001c0004t0004g0321a0001c0007t0001g0322a0001c0017t0001g0319others(3): Show | 6 | HG01255.hp2 HG02280.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.-59+776A>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969108 | ||||||
chr1:177969302
|
G | A | 102 | a0001c0004t0001g0045a0001c0004t0001g0255a0001c0004t0001g0256others(99): Show | 123 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-59+582C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969302 | ||||||
chr1:177969463
|
G | A | 1 | a0001c0021t0001g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-59+421C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969463 | ||||||
chr1:177969577
|
A | G | 41 | a0001c0004t0001g0057a0001c0004t0001g0071a0001c0005t0001g0022others(38): Show | 54 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.-59+307T>C | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969577 | ||||||
chr1:177969611
|
G | A | 1 | a0002c0001t0002g0325 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-59+273C>T | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969611 | ||||||
chr1:177969837
|
C | T | 40 | a0001c0004t0001g0057a0001c0004t0001g0071a0001c0005t0001g0022others(37): Show | 53 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.-59+47G>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969837 | ||||||
chr1:177969838
|
G | T | 4 | a0001c0006t0001g0053a0001c0052t0012g0052a0013c0031t0001g0051others(1): Show | 4 | HG01192.hp1 HG01884.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-59+46C>A | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969838 | ||||||
chr1:177969854
|
G | C | 1 | a0001c0021t0001g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-59+30C>G | SEC16B | ENSG00000120341.19 | transcript | ENST00000308284.11 | protein_coding | 1/25 | chr1 | 177969854 |