geneid | 732 |
---|---|
ensemblid | ENSG00000021852.14 |
hgncid | 1353 |
symbol | C8B |
name | complement C8 beta chain |
refseq_nuc | NM_000066.4 |
refseq_prot | NP_000057.3 |
ensembl_nuc | ENST00000371237.9 |
ensembl_prot | ENSP00000360281.4 |
mane_status | MANE Select |
chr | chr1 |
start | 56929207 |
end | 56966015 |
strand | - |
ver | v1.2 |
region | chr1:56929207-56966015 |
region5000 | chr1:56924207-56971015 |
regionname0 | C8B_chr1_56929207_56966015 |
regionname5000 | C8B_chr1_56924207_56971015 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 591 | 382 | 91 | 68 | 165 | 16 | 41 | 118 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0002 | 0/0 | 591 | 8 | 5 | 2 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0003 | 1/0 | 591 | 6 | 0 | 2 | 0 | 0 | 3 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0004 | 0/0 | 591 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0005 | 0/0 | 591 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0006 | 0/0 | 591 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0007 | 0/0 | 591 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0008 | 0/0 | 591 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0009 | 0/0 | 591 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1776 | 376 | 88 | 67 | 165 | 16 | 39 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
c0002 | 0/0 | 1776 | 8 | 5 | 2 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
c0003 | 1/0 | 1776 | 6 | 0 | 2 | 0 | 0 | 3 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
c0004 | 0/0 | 1776 | 4 | 3 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
c0005 | 0/0 | 1776 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
c0006 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
c0007 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
c0008 | 0/0 | 1776 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
c0009 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
c0010 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
c0011 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 265 | 265 | 85 | 49 | 96 | 10 | 24 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
t0002 | 0/1 | 265 | 133 | 15 | 23 | 69 | 5 | 20 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
t0003 | 0/0 | 265 | 2 | 0 | 0 | 1 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
t0004 | 0/0 | 265 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
t0005 | 0/0 | 265 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0003 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0009 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0030 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0052 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0053 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0054 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0055 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0057 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0061 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0062 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1776 | 376 | 88 | 67 | 165 | 16 | 39 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0001c0004 | 0/0 | 1776 | 4 | 3 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0001c0005 | 0/0 | 1776 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0002c0002 | 0/0 | 1776 | 8 | 5 | 2 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0003c0003 | 1/0 | 1776 | 6 | 0 | 2 | 0 | 0 | 3 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0004c0011 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0005c0010 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0006c0009 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0007c0007 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0008c0006 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0009c0008 | 0/0 | 1776 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2040 | 242 | 74 | 45 | 95 | 10 | 18 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0001c0001t0002 | 0/1 | 2040 | 130 | 14 | 22 | 69 | 5 | 19 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0001c0001t0003 | 0/0 | 2040 | 2 | 0 | 0 | 1 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0001c0001t0004 | 0/0 | 2040 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0001c0001t0005 | 0/0 | 2040 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0001c0004t0001 | 0/0 | 2040 | 4 | 3 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0001c0005t0001 | 0/0 | 2040 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0002c0002t0001 | 0/0 | 2040 | 7 | 5 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0002c0002t0002 | 0/0 | 2040 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0003c0003t0001 | 1/0 | 2040 | 5 | 0 | 1 | 0 | 0 | 3 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0003c0003t0002 | 0/0 | 2040 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0004c0011t0001 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0005c0010t0001 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0006c0009t0001 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0007c0007t0002 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0008c0006t0001 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
a0009c0008t0001 | 0/0 | 2040 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | copy fasta | chr1 | 56924207 | 56971015 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0009 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0030 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0061 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0062 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0003g0052 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0004t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0005t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0001c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0002c0002t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0002c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0003c0003t0001g0054 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0003c0003t0001g0055 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0003c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0004c0011t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0005c0010t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0006c0009t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0007c0007t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0008c0006t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
a0009c0008t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0127 | EUR | GBR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | GBR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0226 | EUR | GBR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | FIN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00621 | hp2 | a0005 | c0010 | t0001 | g0112 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00639 | hp1 | a0003 | c0003 | t0002 | g0247 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0304 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01074 | hp1 | a0003 | c0003 | t0001 | g0054 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01243 | hp1 | a0001 | c0004 | t0001 | g0239 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0205 | EUR | IBS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0052 | EUR | IBS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0204 | EUR | IBS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CDX | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CDX | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0246 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02683 | hp2 | a0009 | c0008 | t0001 | g0290 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0144 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02809 | hp1 | a0001 | c0004 | t0001 | g0160 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02976 | hp2 | a0006 | c0009 | t0001 | g0067 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03209 | hp1 | a0004 | c0011 | t0001 | g0070 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03239 | hp1 | a0003 | c0003 | t0001 | g0055 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03654 | hp2 | a0001 | c0005 | t0001 | g0142 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0305 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03710 | hp1 | a0003 | c0003 | t0001 | g0055 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03831 | hp1 | a0001 | c0005 | t0001 | g0143 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0303 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0287 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | CHB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | CHB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19043 | hp1 | a0008 | c0006 | t0001 | g0248 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ASW | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0301 | AFR | ASW | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | GIH | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0017 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0017 | AFR | USA | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | USA | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | USA | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | USA | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA21309 | hp1 | a0007 | c0007 | t0002 | g0188 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0030 | REF | REF | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0054 | REF | REF | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:56945851
|
C | T | 1 | a0008 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1075G>A | p.Val359Ile | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/12 | 1142/2040 | 1075/1776 | 359/591 | chr1 | 56945851 | ||
chr1:56945914
|
G | A | 1 | a0007 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1012C>T | p.Arg338Cys | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/12 | 1079/2040 | 1012/1776 | 338/591 | chr1 | 56945914 | ||
chr1:56946018
|
T | C | 1 | a0009 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.908A>G | p.His303Arg | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/12 | 975/2040 | 908/1776 | 303/591 | chr1 | 56946018 | ||
chr1:56949590
|
G | C | 1 | a0006 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.829C>G | p.His277Asp | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/12 | 896/2040 | 829/1776 | 277/591 | chr1 | 56949590 | ||
chr1:56949637
|
G | A | 1 | a0002 | 8 | HG01070.hp1 HG01192.hp1 HG01891.hp1 others(5): Show |
missense_variant | MODERATE | c.782C>T | p.Pro261Leu | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/12 | 849/2040 | 782/1776 | 261/591 | chr1 | 56949637 | ||
chr1:56952109
|
G | A | 1 | a0005 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.605C>T | p.Pro202Leu | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/12 | 672/2040 | 605/1776 | 202/591 | chr1 | 56952109 | ||
chr1:56956811
|
C | T | 8 | a0001a0002a0004others(5): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
missense_variant | MODERATE | c.349G>A | p.Gly117Arg | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/12 | 416/2040 | 349/1776 | 117/591 | chr1 | 56956811 | ||
chr1:56956838
|
C | T | 1 | a0002 | 8 | HG01070.hp1 HG01192.hp1 HG01891.hp1 others(5): Show |
missense_variant | MODERATE | c.322G>A | p.Glu108Lys | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/12 | 389/2040 | 322/1776 | 108/591 | chr1 | 56956838 | ||
chr1:56960137
|
G | C | 1 | a0004 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.132C>G | p.Asn44Lys | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/12 | 199/2040 | 132/1776 | 44/591 | chr1 | 56960137 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:56940960
|
T | G | 1 | a0001c0004 | 4 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.1287A>C | p.Gly429Gly | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/12 | 1354/2040 | 1287/1776 | 429/591 | chr1 | 56940960 | ||
chr1:56956884
|
G | A | 1 | a0001c0005 | 2 | HG03654.hp2 HG03831.hp1 |
synonymous_variant | LOW | c.276C>T | p.Pro92Pro | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/12 | 343/2040 | 276/1776 | 92/591 | chr1 | 56956884 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:56929239
|
T | A | 1 | a0001c0001t0004 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 12/12 | 165 | chr1 | 56929239 | |||||
chr1:56929318
|
G | T | 1 | a0001c0001t0003 | 2 | HG00423.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*86C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 12/12 | 86 | chr1 | 56929318 | |||||
chr1:56929320
|
T | G | 1 | a0001c0001t0003 | 2 | HG00423.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*84A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 12/12 | 84 | chr1 | 56929320 | |||||
chr1:56929347
|
A | G | 4 | a0001c0001t0002a0002c0002t0002a0003c0003t0002others(1): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*57T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 12/12 | 57 | chr1 | 56929347 | |||||
chr1:56966011
|
G | A | 1 | a0001c0001t0005 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-63C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/12 | 63 | chr1 | 56966011 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:56929578
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1622-20A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929578 | ||||||
chr1:56929621
|
G | A | 1 | a0001c0001t0001g0025 | 2 | HG00323.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1622-63C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929621 | ||||||
chr1:56929648
|
C | T | 19 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0057others(16): Show | 22 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-90G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929648 | ||||||
chr1:56929748
|
C | G | 99 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(96): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1622-190G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929748 | ||||||
chr1:56929761
|
C | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 94 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1622-203G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929761 | ||||||
chr1:56929780
|
C | A | 1 | a0004c0011t0001g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1622-222G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929780 | ||||||
chr1:56929827
|
T | C | 2 | a0001c0001t0002g0127a0001c0001t0002g0237 | 2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1622-269A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929827 | ||||||
chr1:56929865
|
T | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0042others(13): Show | 23 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.1622-307A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929865 | ||||||
chr1:56929919
|
G | C | 100 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1622-361C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929919 | ||||||
chr1:56930012
|
T | G | 100 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1622-454A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930012 | ||||||
chr1:56930028
|
G | A | 100 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1622-470C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930028 | ||||||
chr1:56930032
|
C | A | 1 | a0002c0002t0001g0233 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1622-474G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930032 | ||||||
chr1:56930045
|
C | A | 1 | a0001c0001t0002g0287 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1622-487G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930045 | ||||||
chr1:56930077
|
G | C | 100 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1622-519C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930077 | ||||||
chr1:56930341
|
A | G | 100 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1622-783T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930341 | ||||||
chr1:56930603
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1622-1045G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930603 | ||||||
chr1:56930780
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0098a0001c0001t0001g0201others(3): Show | 10 | HG02071.hp2 NA18947.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1621+1030T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930780 | ||||||
chr1:56930869
|
C | T | 104 | a0001c0001t0001g0016a0001c0001t0001g0080a0001c0001t0001g0177others(101): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1621+941G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930869 | ||||||
chr1:56930894
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1621+916G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930894 | ||||||
chr1:56930896
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1621+914T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930896 | ||||||
chr1:56930977
|
G | A | 1 | a0001c0001t0002g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1621+833C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930977 | ||||||
chr1:56931020
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1621+790T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931020 | ||||||
chr1:56931366
|
A | G | 100 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1621+444T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931366 | ||||||
chr1:56931409
|
C | T | 99 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(96): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1621+401G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931409 | ||||||
chr1:56931410
|
G | T | 1 | a0001c0001t0002g0190 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1621+400C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931410 | ||||||
chr1:56931443
|
T | C | 1 | a0004c0011t0001g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1621+367A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931443 | ||||||
chr1:56931510
|
T | C | 100 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1621+300A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931510 | ||||||
chr1:56931628
|
G | A | 100 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1621+182C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931628 | ||||||
chr1:56931679
|
C | T | 1 | a0001c0001t0002g0274 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1621+131G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931679 | ||||||
chr1:56931771
|
C | A | 13 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0066others(10): Show | 15 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1621+39G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931771 | ||||||
chr1:56931900
|
AGT | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0203a0001c0001t0001g0210 | 3 | HG02071.hp2 NA18990.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1553-24_1553-23del others(2): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56931900 | ||||||
chr1:56931969
|
G | T | 10 | a0001c0001t0001g0072a0001c0001t0001g0179a0001c0001t0001g0186others(7): Show | 11 | HG01255.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1553-91C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56931969 | ||||||
chr1:56932014
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1553-136C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932014 | ||||||
chr1:56932060
|
C | T | 3 | a0001c0001t0001g0121a0001c0005t0001g0142a0001c0005t0001g0143 | 3 | HG02145.hp1 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1553-182G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932060 | ||||||
chr1:56932065
|
G | C | 100 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1553-187C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932065 | ||||||
chr1:56932153
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1553-275T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932153 | ||||||
chr1:56932174
|
A | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0185a0001c0001t0001g0296 | 3 | HG02145.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1553-296T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932174 | ||||||
chr1:56932259
|
C | A | 2 | a0001c0001t0002g0127a0001c0001t0002g0237 | 2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1553-381G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932259 | ||||||
chr1:56932594
|
C | T | 15 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0179others(12): Show | 17 | HG01243.hp1 HG01255.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1553-716G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932594 | ||||||
chr1:56932615
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1552+720A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932615 | ||||||
chr1:56932658
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1552+677G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932658 | ||||||
chr1:56932705
|
C | T | 102 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0002g0002others(99): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1552+630G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932705 | ||||||
chr1:56932768
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1552+567C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932768 | ||||||
chr1:56933000
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1552+335G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56933000 | ||||||
chr1:56933029
|
G | A | 1 | a0001c0001t0002g0036 | 2 | NA18950.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1552+306C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56933029 | ||||||
chr1:56933525
|
A | C | 1 | a0001c0001t0002g0190 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1399-37T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933525 | ||||||
chr1:56933562
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1399-74C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933562 | ||||||
chr1:56933577
|
C | T | 3 | a0001c0001t0001g0121a0001c0005t0001g0142a0001c0005t0001g0143 | 3 | HG02145.hp1 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1399-89G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933577 | ||||||
chr1:56933776
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1399-288C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933776 | ||||||
chr1:56933863
|
G | T | 100 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1399-375C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933863 | ||||||
chr1:56933949
|
T | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(266): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1399-461A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933949 | ||||||
chr1:56934140
|
CTTT | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1399-655_1399-653d others(5): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934140 | ||||||
chr1:56934142
|
T | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0185a0001c0001t0001g0296 | 3 | HG02145.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1399-654A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934142 | ||||||
chr1:56934164
|
C | CT | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1399-677dupA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934164 | ||||||
chr1:56934168
|
T | TA | 3 | a0001c0001t0001g0189a0002c0002t0001g0184a0002c0002t0001g0233 | 3 | HG01192.hp1 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1399-681_1399-680i others(3): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934168 | ||||||
chr1:56934214
|
A | G | 1 | a0003c0003t0002g0247 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1399-726T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934214 | ||||||
chr1:56934234
|
C | T | 13 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0066others(10): Show | 15 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1399-746G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934234 | ||||||
chr1:56934246
|
C | A | 1 | a0001c0001t0001g0264 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1399-758G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934246 | ||||||
chr1:56934253
|
T | A | 102 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0002g0002others(99): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1399-765A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934253 | ||||||
chr1:56934405
|
G | A | 19 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0057others(16): Show | 22 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.1399-917C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934405 | ||||||
chr1:56934462
|
A | G | 1 | a0004c0011t0001g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1399-974T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934462 | ||||||
chr1:56934564
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1399-1076G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934564 | ||||||
chr1:56934587
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0138a0001c0001t0001g0298 | 4 | HG02257.hp2 HG02280.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1399-1099G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934587 | ||||||
chr1:56934588
|
G | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0042others(13): Show | 23 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.1399-1100C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934588 | ||||||
chr1:56934629
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1399-1141C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934629 | ||||||
chr1:56934902
|
A | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1399-1414T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934902 | ||||||
chr1:56934997
|
G | A | 4 | a0001c0001t0001g0299a0001c0004t0001g0017a0001c0004t0001g0160others(1): Show | 5 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1399-1509C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934997 | ||||||
chr1:56935311
|
C | T | 23 | a0001c0001t0001g0024a0001c0001t0001g0085a0001c0001t0001g0087others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1399-1823G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935311 | ||||||
chr1:56935338
|
T | A | 1 | a0001c0001t0001g0295 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1399-1850A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935338 | ||||||
chr1:56935348
|
C | T | 19 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0083others(16): Show | 20 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1399-1860G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935348 | ||||||
chr1:56935375
|
C | T | 3 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0154 | 3 | HG00639.hp2 HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1399-1887G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935375 | ||||||
chr1:56935437
|
C | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0042others(13): Show | 23 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.1399-1949G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935437 | ||||||
chr1:56935442
|
C | G | 3 | a0001c0001t0001g0057a0001c0001t0001g0073a0009c0008t0001g0290 | 4 | HG02683.hp2 HG02735.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-1954G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935442 | ||||||
chr1:56936058
|
G | T | 1 | a0001c0001t0001g0299 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1399-2570C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936058 | ||||||
chr1:56936096
|
A | C | 1 | a0001c0001t0001g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1399-2608T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936096 | ||||||
chr1:56936245
|
A | G | 6 | a0001c0001t0001g0057a0001c0001t0001g0073a0001c0001t0001g0121others(3): Show | 7 | HG02145.hp1 HG02683.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-2757T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936245 | ||||||
chr1:56936306
|
A | T | 2 | a0001c0001t0002g0127a0001c0001t0002g0237 | 2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1399-2818T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936306 | ||||||
chr1:56936309
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1399-2821A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936309 | ||||||
chr1:56936319
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1399-2831A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936319 | ||||||
chr1:56936511
|
TA | T | 83 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(80): Show | 116 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1399-3024delT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936511 | ||||||
chr1:56936513
|
AAT | A | 7 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0002g0076others(4): Show | 7 | HG01515.hp2 HG03098.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1399-3027_1399-302 others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936513 | ||||||
chr1:56936514
|
A | T | 10 | a0001c0001t0002g0063a0001c0001t0002g0078a0001c0001t0002g0093others(7): Show | 10 | HG00099.hp2 HG01106.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1399-3026T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936514 | ||||||
chr1:56936514
|
AT | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(100): Show | 139 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1399-3027delA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936514 | ||||||
chr1:56936514
|
ATT | A | 33 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 41 | HG01109.hp1 HG01109.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.1399-3028_1399-302 others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936514 | ||||||
chr1:56936601
|
C | CT | 25 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0096others(22): Show | 29 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.1399-3114dupA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936601 | ||||||
chr1:56936605
|
T | A | 1 | a0002c0002t0001g0184 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1399-3117A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936605 | ||||||
chr1:56936697
|
C | T | 4 | a0001c0001t0001g0299a0001c0004t0001g0017a0001c0004t0001g0160others(1): Show | 5 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1399-3209G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936697 | ||||||
chr1:56936974
|
T | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0185a0001c0001t0001g0296 | 3 | HG02145.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1399-3486A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936974 | ||||||
chr1:56937126
|
G | C | 1 | a0001c0001t0002g0129 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1399-3638C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937126 | ||||||
chr1:56937223
|
C | T | 2 | a0001c0001t0002g0099a0001c0001t0002g0123 | 2 | NA18948.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1398+3626G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937223 | ||||||
chr1:56937289
|
C | T | 1 | a0007c0007t0002g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1398+3560G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937289 | ||||||
chr1:56937488
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0059a0001c0001t0001g0092 | 5 | NA18945.hp2 NA18946.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1398+3361A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937488 | ||||||
chr1:56937674
|
ATT | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0179a0001c0001t0001g0186others(7): Show | 11 | HG01255.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1398+3173_1398+317 others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937674 | ||||||
chr1:56937677
|
T | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0179a0001c0001t0001g0186others(7): Show | 11 | HG01255.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1398+3172A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937677 | ||||||
chr1:56937763
|
AT | A | 32 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0029others(29): Show | 40 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.1398+3085delA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937763 | ||||||
chr1:56937981
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1398+2868A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937981 | ||||||
chr1:56938130
|
C | G | 101 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0002g0002others(98): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1398+2719G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938130 | ||||||
chr1:56938137
|
T | C | 1 | a0001c0001t0001g0019 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1398+2712A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938137 | ||||||
chr1:56938226
|
A | G | 1 | a0001c0001t0001g0058 | 2 | HG02155.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1398+2623T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938226 | ||||||
chr1:56938254
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1398+2595A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938254 | ||||||
chr1:56938322
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1398+2527A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938322 | ||||||
chr1:56938428
|
A | C | 2 | a0001c0001t0003g0052a0002c0002t0001g0304 | 3 | HG00423.hp2 HG01070.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1398+2421T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938428 | ||||||
chr1:56938716
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1398+2133A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938716 | ||||||
chr1:56938828
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1398+2021A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938828 | ||||||
chr1:56938891
|
G | GA | 100 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0002g0002others(97): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1398+1957dupT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938891 | ||||||
chr1:56939066
|
C | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1398+1783G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939066 | ||||||
chr1:56939222
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02895.hp2 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1398+1627G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939222 | ||||||
chr1:56939232
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1398+1617A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939232 | ||||||
chr1:56939285
|
G | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1398+1564C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939285 | ||||||
chr1:56939422
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1398+1427T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939422 | ||||||
chr1:56939550
|
A | T | 99 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(96): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1398+1299T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939550 | ||||||
chr1:56939583
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1398+1266T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939583 | ||||||
chr1:56939631
|
C | T | 1 | a0007c0007t0002g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1398+1218G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939631 | ||||||
chr1:56939676
|
T | C | 6 | a0001c0001t0001g0057a0001c0001t0001g0073a0001c0001t0001g0121others(3): Show | 7 | HG02145.hp1 HG02683.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+1173A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939676 | ||||||
chr1:56939952
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1398+897C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939952 | ||||||
chr1:56940015
|
CGT | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1398+832_1398+833d others(4): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940015 | ||||||
chr1:56940030
|
G | C | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1398+819C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940030 | ||||||
chr1:56940048
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1398+801G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940048 | ||||||
chr1:56940111
|
G | A | 1 | a0001c0001t0002g0061 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1398+738C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940111 | ||||||
chr1:56940132
|
T | G | 4 | a0001c0001t0002g0122a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 4 | HG03239.hp2 HG04184.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398+717A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940132 | ||||||
chr1:56940399
|
TA | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(9): Show | 14 | HG00639.hp2 HG01257.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1398+449delT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940399 | ||||||
chr1:56940500
|
T | A | 1 | a0004c0011t0001g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1398+349A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940500 | ||||||
chr1:56940536
|
C | T | 1 | a0001c0004t0001g0017 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1398+313G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940536 | ||||||
chr1:56940537
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265 | 3 | HG02559.hp2 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1398+312G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940537 | ||||||
chr1:56940538
|
C | A | 13 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 14 | HG02622.hp1 HG02647.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1398+311G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940538 | ||||||
chr1:56940541
|
A | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0066others(11): Show | 16 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1398+308T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940541 | ||||||
chr1:56940574
|
A | AAAG | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1398+272_1398+274d others(5): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940574 | ||||||
chr1:56940719
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1398+130A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940719 | ||||||
chr1:56940840
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0231 | 2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1398+9C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940840 | ||||||
chr1:56941157
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1235-145T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941157 | ||||||
chr1:56941193
|
C | T | 3 | a0001c0001t0001g0121a0001c0005t0001g0142a0001c0005t0001g0143 | 3 | HG02145.hp1 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1235-181G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941193 | ||||||
chr1:56941254
|
T | C | 99 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(96): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1235-242A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941254 | ||||||
chr1:56941308
|
A | T | 1 | a0001c0001t0002g0090 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1235-296T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941308 | ||||||
chr1:56941494
|
GTAGA | G | 10 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0045others(7): Show | 14 | HG01109.hp1 HG01109.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1235-486_1235-483d others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | ||||||
chr1:56941494
|
GTAGATAG others(9): Show |
G | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 108 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1235-498_1235-483d others(18): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | ||||||
chr1:56941494
|
GTAGATAG others(13): Show |
G | 20 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0109others(17): Show | 23 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1235-502_1235-483d others(22): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | ||||||
chr1:56941494
|
GTAGATAG others(17): Show |
G | 15 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0042others(12): Show | 22 | HG00323.hp1 HG00408.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1235-506_1235-483d others(26): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | ||||||
chr1:56941494
|
GTAGATAG others(21): Show |
G | 4 | a0001c0001t0001g0121a0001c0001t0001g0194a0001c0005t0001g0142others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-510_1235-483d others(30): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | ||||||
chr1:56941494
|
GTAGATAG others(25): Show |
G | 1 | a0001c0001t0001g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1235-514_1235-483d others(34): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | ||||||
chr1:56941497
|
GATAGATA others(5): Show |
G | 15 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0064others(12): Show | 18 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1235-497_1235-486d others(14): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941497 | ||||||
chr1:56941501
|
GATAGATA others(1): Show |
G | 3 | a0001c0001t0001g0029a0001c0001t0001g0103a0001c0001t0001g0285 | 4 | HG02451.hp1 HG02647.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-497_1235-490d others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941501 | ||||||
chr1:56941505
|
G | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0187 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1235-493C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941505 | ||||||
chr1:56941509
|
C | CATAG | 31 | a0001c0001t0001g0231a0001c0001t0001g0293a0001c0001t0002g0011others(28): Show | 39 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.1235-501_1235-498d others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | ||||||
chr1:56941509
|
C | CATAGATA others(1): Show |
9 | a0001c0001t0001g0149a0001c0001t0001g0221a0001c0001t0001g0254others(6): Show | 11 | HG00544.hp2 HG00639.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1235-505_1235-498d others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | ||||||
chr1:56941509
|
C | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0187 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1235-497G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | ||||||
chr1:56941509
|
CATAG | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0053others(30): Show | 48 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.1235-501_1235-498d others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | ||||||
chr1:56941509
|
CATAGATA others(1): Show |
C | 6 | a0001c0001t0001g0108a0001c0001t0001g0115a0001c0001t0001g0209others(3): Show | 6 | HG00639.hp2 HG00642.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1235-505_1235-498d others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | ||||||
chr1:56941509
|
CATAGATA others(13): Show |
C | 16 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0179others(13): Show | 18 | HG01243.hp1 HG01255.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1235-517_1235-498d others(22): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | ||||||
chr1:56941513
|
G | C | 1 | a0001c0001t0001g0029 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1235-501C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941513 | ||||||
chr1:56941548
|
A | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0200 | 5 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1235-536T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941548 | ||||||
chr1:56941725
|
A | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0066others(11): Show | 16 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1235-713T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941725 | ||||||
chr1:56941811
|
C | T | 99 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(96): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1235-799G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941811 | ||||||
chr1:56941814
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1235-802T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941814 | ||||||
chr1:56941963
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1235-951T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941963 | ||||||
chr1:56942219
|
T | C | 1 | a0004c0011t0001g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1235-1207A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942219 | ||||||
chr1:56942261
|
CTAAG | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1235-1253_1235-125 others(8): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942261 | ||||||
chr1:56942422
|
C | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 14 | HG02622.hp1 HG02647.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1234+1274G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942422 | ||||||
chr1:56942448
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1234+1248A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942448 | ||||||
chr1:56942501
|
G | A | 2 | a0001c0001t0001g0189a0002c0002t0001g0184 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1234+1195C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942501 | ||||||
chr1:56942507
|
G | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1234+1189C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942507 | ||||||
chr1:56942519
|
A | G | 20 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0057others(17): Show | 23 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1234+1177T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942519 | ||||||
chr1:56942551
|
A | G | 20 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0057others(17): Show | 23 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1234+1145T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942551 | ||||||
chr1:56942566
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1234+1130C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942566 | ||||||
chr1:56942605
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1234+1091C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942605 | ||||||
chr1:56942634
|
G | C | 1 | a0001c0001t0001g0299 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1234+1062C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942634 | ||||||
chr1:56942656
|
G | A | 1 | a0007c0007t0002g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1234+1040C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942656 | ||||||
chr1:56942668
|
C | T | 2 | a0001c0001t0002g0275a0001c0001t0002g0276 | 2 | NA18612.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1234+1028G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942668 | ||||||
chr1:56942750
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1234+946G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942750 | ||||||
chr1:56942806
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1234+890T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942806 | ||||||
chr1:56942838
|
A | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265 | 3 | HG02559.hp2 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1234+858T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942838 | ||||||
chr1:56942964
|
C | T | 1 | a0004c0011t0001g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1234+732G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942964 | ||||||
chr1:56943052
|
C | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0230 | 2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1234+644G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943052 | ||||||
chr1:56943361
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1234+335G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943361 | ||||||
chr1:56943403
|
A | G | 14 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0119others(11): Show | 15 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.1234+293T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943403 | ||||||
chr1:56943421
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1234+275T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943421 | ||||||
chr1:56943485
|
T | C | 7 | a0001c0001t0001g0086a0001c0001t0001g0213a0001c0001t0001g0216others(4): Show | 7 | HG02572.hp1 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1234+211A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943485 | ||||||
chr1:56943531
|
G | A | 1 | a0001c0001t0001g0013 | 3 | HG00733.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1234+165C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943531 | ||||||
chr1:56943536
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0203a0001c0001t0001g0210 | 3 | HG02071.hp2 NA18990.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1234+160G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943536 | ||||||
chr1:56943654
|
T | C | 12 | a0001c0001t0001g0024a0001c0001t0001g0085a0001c0001t0001g0087others(9): Show | 13 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1234+42A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943654 | ||||||
chr1:56943656
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0155others(1): Show | 5 | HG00323.hp1 HG01168.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234+40T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943656 | ||||||
chr1:56943691
|
C | G | 1 | a0001c0001t0002g0062 | 2 | HG01256.hp1 HG01258.hp2 |
splice_region_variant&intron_variant | LOW | c.1234+5G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943691 | ||||||
chr1:56943911
|
T | A | 6 | a0001c0001t0001g0089a0001c0001t0001g0183a0001c0001t0001g0232others(3): Show | 6 | HG01361.hp1 HG02572.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106-87A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56943911 | ||||||
chr1:56943932
|
G | A | 6 | a0001c0001t0001g0089a0001c0001t0001g0183a0001c0001t0001g0232others(3): Show | 6 | HG01361.hp1 HG02572.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106-108C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56943932 | ||||||
chr1:56943989
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265 | 3 | HG02559.hp2 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1106-165G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56943989 | ||||||
chr1:56944055
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1106-231C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944055 | ||||||
chr1:56944071
|
T | C | 32 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0060others(29): Show | 37 | HG00597.hp1 HG00639.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1106-247A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944071 | ||||||
chr1:56944141
|
C | G | 1 | a0001c0001t0002g0165 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1106-317G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944141 | ||||||
chr1:56944287
|
G | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265 | 3 | HG02559.hp2 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1106-463C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944287 | ||||||
chr1:56944340
|
C | T | 10 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0060others(7): Show | 13 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1106-516G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944340 | ||||||
chr1:56944369
|
C | G | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0064others(5): Show | 10 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1106-545G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944369 | ||||||
chr1:56944398
|
T | TA | 4 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-575dupT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944398 | ||||||
chr1:56944472
|
A | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1106-648T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944472 | ||||||
chr1:56944598
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1106-774T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944598 | ||||||
chr1:56944628
|
C | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | NA18988.hp1 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1106-804G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944628 | ||||||
chr1:56945024
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1105+797A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945024 | ||||||
chr1:56945077
|
C | A | 4 | a0001c0001t0002g0252a0001c0001t0002g0261a0001c0001t0002g0288others(1): Show | 4 | HG00597.hp2 HG00621.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105+744G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945077 | ||||||
chr1:56945097
|
C | A | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1105+724G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945097 | ||||||
chr1:56945105
|
T | C | 4 | a0001c0001t0001g0182a0001c0001t0001g0225a0001c0001t0001g0296others(1): Show | 4 | NA18940.hp1 NA19060.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105+716A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945105 | ||||||
chr1:56945229
|
C | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(47): Show | 62 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1105+592G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945229 | ||||||
chr1:56945452
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1105+369G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945452 | ||||||
chr1:56945527
|
GCAGGAAG others(16): Show |
G | 2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1105+271_1105+293d others(25): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945527 | ||||||
chr1:56945742
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1105+79C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945742 | ||||||
chr1:56946106
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0002g0035a0001c0001t0002g0172 | 4 | HG01515.hp1 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.865-45C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946106 | ||||||
chr1:56946456
|
G | A | 1 | a0002c0002t0001g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.865-395C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946456 | ||||||
chr1:56946523
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.865-462T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946523 | ||||||
chr1:56946587
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(71): Show | 111 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.865-526G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946587 | ||||||
chr1:56946795
|
T | C | 3 | a0001c0001t0001g0269a0001c0001t0002g0002a0001c0001t0002g0302 | 8 | HG01081.hp1 HG01884.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.865-734A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946795 | ||||||
chr1:56946816
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.865-755T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946816 | ||||||
chr1:56947069
|
T | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.865-1008A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947069 | ||||||
chr1:56947175
|
G | T | 110 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(107): Show | 145 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.865-1114C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947175 | ||||||
chr1:56947274
|
T | C | 49 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(46): Show | 61 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.865-1213A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947274 | ||||||
chr1:56947298
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.865-1237A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947298 | ||||||
chr1:56947522
|
C | G | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.865-1461G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947522 | ||||||
chr1:56947660
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.865-1599C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947660 | ||||||
chr1:56947775
|
C | CA | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0064others(23): Show | 30 | HG00597.hp1 HG00639.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.865-1715dupT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947775 | ||||||
chr1:56947869
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.864+1686A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947869 | ||||||
chr1:56947919
|
A | G | 13 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.864+1636T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947919 | ||||||
chr1:56947951
|
CA | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(47): Show | 62 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.864+1603delT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947951 | ||||||
chr1:56947952
|
A | AAAAC | 144 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(141): Show | 184 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.864+1599_864+1602d others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947952 | ||||||
chr1:56948039
|
A | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG01175.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.864+1516T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948039 | ||||||
chr1:56948095
|
G | A | 194 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(191): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.864+1460C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948095 | ||||||
chr1:56948175
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.864+1380C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948175 | ||||||
chr1:56948258
|
CTATT | C | 4 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+1293_864+1296d others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948258 | ||||||
chr1:56948569
|
T | C | 2 | a0001c0005t0001g0142a0001c0005t0001g0143 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.864+986A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948569 | ||||||
chr1:56948641
|
G | A | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.864+914C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948641 | ||||||
chr1:56948763
|
A | G | 4 | a0001c0001t0001g0182a0001c0001t0001g0225a0001c0001t0001g0296others(1): Show | 4 | NA18940.hp1 NA19060.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+792T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948763 | ||||||
chr1:56948880
|
A | G | 4 | a0001c0001t0001g0182a0001c0001t0001g0225a0001c0001t0001g0296others(1): Show | 4 | NA18940.hp1 NA19060.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+675T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948880 | ||||||
chr1:56949008
|
A | AT | 93 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(90): Show | 126 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.864+546dupA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949008 | ||||||
chr1:56949008
|
AT | A | 23 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(20): Show | 27 | HG00639.hp2 HG01070.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.864+546delA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949008 | ||||||
chr1:56949073
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.864+482G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949073 | ||||||
chr1:56949152
|
A | G | 1 | a0001c0001t0002g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.864+403T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949152 | ||||||
chr1:56949341
|
T | G | 1 | a0001c0001t0002g0102 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.864+214A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949341 | ||||||
chr1:56949527
|
C | T | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0064others(23): Show | 30 | HG00597.hp1 HG00639.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.864+28G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949527 | ||||||
chr1:56949778
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.667-26A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56949778 | ||||||
chr1:56949920
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0210 | 2 | NA18990.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.667-168G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56949920 | ||||||
chr1:56949921
|
A | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(191): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.667-169T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56949921 | ||||||
chr1:56949922
|
G | T | 25 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0064others(22): Show | 29 | HG00597.hp1 HG00639.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.667-170C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56949922 | ||||||
chr1:56950050
|
G | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(70): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.667-298C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950050 | ||||||
chr1:56950066
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0210 | 2 | NA18990.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.667-314C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950066 | ||||||
chr1:56950293
|
A | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(191): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.667-541T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950293 | ||||||
chr1:56950472
|
A | G | 2 | a0002c0002t0001g0051a0002c0002t0001g0233 | 3 | HG01192.hp1 HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.667-720T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950472 | ||||||
chr1:56950529
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.667-777C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950529 | ||||||
chr1:56950579
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.667-827G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950579 | ||||||
chr1:56950652
|
A | T | 1 | a0001c0001t0001g0300 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.667-900T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950652 | ||||||
chr1:56950662
|
G | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(88): Show | 124 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.667-910C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950662 | ||||||
chr1:56950774
|
C | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.667-1022G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950774 | ||||||
chr1:56950856
|
G | A | 13 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.667-1104C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950856 | ||||||
chr1:56950927
|
A | G | 110 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(107): Show | 145 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.666+1121T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950927 | ||||||
chr1:56950960
|
C | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(74): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.666+1088G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950960 | ||||||
chr1:56950978
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.666+1070T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950978 | ||||||
chr1:56951335
|
A | C | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.666+713T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951335 | ||||||
chr1:56951411
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.666+637G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951411 | ||||||
chr1:56951419
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.666+629T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951419 | ||||||
chr1:56951435
|
T | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(191): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.666+613A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951435 | ||||||
chr1:56951685
|
G | A | 13 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.666+363C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951685 | ||||||
chr1:56951711
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0001g0225a0001c0001t0001g0297 | 3 | NA18940.hp1 NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.666+337A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951711 | ||||||
chr1:56951919
|
C | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(48): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.666+129G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951919 | ||||||
chr1:56951960
|
G | GGGATGTG others(14): Show |
194 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(191): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.666+87_666+88insTG others(19): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951960 | ||||||
chr1:56952219
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.534-39A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952219 | ||||||
chr1:56952257
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.534-77G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952257 | ||||||
chr1:56952383
|
G | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0155others(2): Show | 6 | HG00323.hp1 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.534-203C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952383 | ||||||
chr1:56952512
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.534-332A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952512 | ||||||
chr1:56952593
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.534-413G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952593 | ||||||
chr1:56952687
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.534-507C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952687 | ||||||
chr1:56952711
|
C | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.534-531G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952711 | ||||||
chr1:56952740
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(48): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.534-560C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952740 | ||||||
chr1:56952876
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0238a0001c0004t0001g0239 | 3 | HG01109.hp2 HG01243.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.534-696G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952876 | ||||||
chr1:56952881
|
T | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-701A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952881 | ||||||
chr1:56952891
|
T | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0189 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.534-711A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952891 | ||||||
chr1:56952984
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.534-804C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952984 | ||||||
chr1:56953053
|
G | A | 2 | a0002c0002t0001g0304a0002c0002t0002g0303 | 2 | HG01070.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.534-873C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953053 | ||||||
chr1:56953096
|
C | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-916G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953096 | ||||||
chr1:56953103
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.534-923A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953103 | ||||||
chr1:56953384
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.534-1204C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953384 | ||||||
chr1:56953553
|
C | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(188): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.533+1133G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953553 | ||||||
chr1:56953614
|
G | A | 157 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(154): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.533+1072C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953614 | ||||||
chr1:56953709
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.533+977C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953709 | ||||||
chr1:56953858
|
G | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 12 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.533+828C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953858 | ||||||
chr1:56953884
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.533+802A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953884 | ||||||
chr1:56953934
|
T | C | 195 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(192): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.533+752A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953934 | ||||||
chr1:56953997
|
T | A | 1 | a0001c0001t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.533+689A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953997 | ||||||
chr1:56954131
|
G | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG01175.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.533+555C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954131 | ||||||
chr1:56954209
|
A | G | 13 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.533+477T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954209 | ||||||
chr1:56954274
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG01175.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.533+412G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954274 | ||||||
chr1:56954334
|
A | C | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.533+352T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954334 | ||||||
chr1:56954370
|
T | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(154): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.533+316A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954370 | ||||||
chr1:56954403
|
C | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG01175.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.533+283G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954403 | ||||||
chr1:56954429
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0257 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.533+257C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954429 | ||||||
chr1:56954486
|
A | G | 1 | a0001c0001t0002g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.533+200T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954486 | ||||||
chr1:56954513
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.533+173T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954513 | ||||||
chr1:56954625
|
C | A | 2 | a0001c0005t0001g0142a0001c0005t0001g0143 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.533+61G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954625 | ||||||
chr1:56954625
|
C | T | 2 | a0001c0001t0002g0090a0001c0001t0002g0117 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.533+61G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954625 | ||||||
chr1:56954663
|
G | A | 3 | a0001c0001t0001g0291a0001c0005t0001g0142a0001c0005t0001g0143 | 3 | HG02083.hp2 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.533+23C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954663 | ||||||
chr1:56954856
|
G | A | 2 | a0001c0001t0002g0267a0001c0001t0002g0292 | 2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.392-29C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56954856 | ||||||
chr1:56954954
|
A | G | 7 | a0002c0002t0001g0051a0002c0002t0001g0184a0002c0002t0001g0233others(4): Show | 8 | HG01070.hp1 HG01192.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.392-127T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56954954 | ||||||
chr1:56955094
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.392-267C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955094 | ||||||
chr1:56955220
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.392-393C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955220 | ||||||
chr1:56955265
|
C | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0177 | 4 | NA18943.hp1 NA18992.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-438G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955265 | ||||||
chr1:56955284
|
A | G | 157 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(154): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.392-457T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955284 | ||||||
chr1:56955414
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.392-587T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955414 | ||||||
chr1:56955436
|
C | T | 4 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-609G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955436 | ||||||
chr1:56955493
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(154): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.392-666G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955493 | ||||||
chr1:56955648
|
A | T | 1 | a0001c0001t0001g0019 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.392-821T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955648 | ||||||
chr1:56955664
|
A | G | 195 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(192): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.392-837T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955664 | ||||||
chr1:56955718
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.392-891G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955718 | ||||||
chr1:56955838
|
A | G | 11 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 12 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.391+931T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955838 | ||||||
chr1:56956083
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.391+686G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956083 | ||||||
chr1:56956102
|
A | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(185): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.391+667T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956102 | ||||||
chr1:56956102
|
A | T | 7 | a0002c0002t0001g0051a0002c0002t0001g0184a0002c0002t0001g0233others(4): Show | 8 | HG01070.hp1 HG01192.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+667T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956102 | ||||||
chr1:56956111
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.391+658A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956111 | ||||||
chr1:56956314
|
C | T | 195 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(192): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.391+455G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956314 | ||||||
chr1:56956318
|
A | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(48): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.391+451T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956318 | ||||||
chr1:56956405
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.391+364T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956405 | ||||||
chr1:56956448
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+321C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956448 | ||||||
chr1:56956543
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.391+226G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956543 | ||||||
chr1:56956545
|
T | C | 195 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(192): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.391+224A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956545 | ||||||
chr1:56956745
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.391+24A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956745 | ||||||
chr1:56956930
|
G | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.250-20C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56956930 | ||||||
chr1:56956966
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.250-56C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56956966 | ||||||
chr1:56957123
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.250-213T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957123 | ||||||
chr1:56957258
|
T | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(88): Show | 124 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.250-348A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957258 | ||||||
chr1:56957271
|
CCAGTTCA others(30): Show |
C | 1 | a0001c0001t0001g0259 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.250-398_250-362del others(37): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957271 | ||||||
chr1:56957834
|
C | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.250-924G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957834 | ||||||
chr1:56957940
|
TCTGACAG others(10): Show |
T | 1 | a0001c0001t0001g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.250-1047_250-1031d others(19): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957940 | ||||||
chr1:56957962
|
C | G | 191 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(188): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.250-1052G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957962 | ||||||
chr1:56957992
|
T | G | 1 | a0001c0004t0001g0160 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.250-1082A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957992 | ||||||
chr1:56958068
|
T | C | 4 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-1158A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958068 | ||||||
chr1:56958110
|
T | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(48): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.250-1200A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958110 | ||||||
chr1:56958495
|
G | GA | 5 | a0001c0001t0001g0016a0001c0001t0001g0163a0001c0001t0001g0164others(2): Show | 7 | HG01891.hp2 HG02965.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+1524dupT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958495 | ||||||
chr1:56958510
|
A | G | 4 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+1510T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958510 | ||||||
chr1:56958551
|
G | T | 4 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+1469C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958551 | ||||||
chr1:56958595
|
GC | G | 12 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(9): Show | 14 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+1424delG | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958595 | ||||||
chr1:56958597
|
T | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(9): Show | 14 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+1423A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958597 | ||||||
chr1:56958623
|
T | G | 3 | a0001c0001t0001g0071a0001c0004t0001g0017a0004c0011t0001g0070 | 4 | HG02055.hp1 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+1397A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958623 | ||||||
chr1:56959046
|
A | G | 26 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0064others(23): Show | 30 | HG00597.hp1 HG01256.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.249+974T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959046 | ||||||
chr1:56959062
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.249+958A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959062 | ||||||
chr1:56959145
|
T | C | 1 | a0001c0001t0002g0030 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.249+875A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959145 | ||||||
chr1:56959365
|
G | A | 3 | a0001c0001t0001g0173a0001c0001t0001g0217a0001c0001t0002g0036 | 4 | NA18950.hp1 NA18966.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+655C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959365 | ||||||
chr1:56959471
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+549C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959471 | ||||||
chr1:56959552
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.249+468C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959552 | ||||||
chr1:56959567
|
A | G | 1 | a0001c0001t0002g0267 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.249+453T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959567 | ||||||
chr1:56959587
|
T | G | 1 | a0001c0001t0002g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.249+433A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959587 | ||||||
chr1:56959616
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.249+404G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959616 | ||||||
chr1:56959648
|
G | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(9): Show | 14 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+372C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959648 | ||||||
chr1:56959745
|
T | C | 6 | a0001c0001t0001g0182a0001c0001t0001g0225a0001c0001t0001g0296others(3): Show | 7 | HG02738.hp1 HG03491.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+275A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959745 | ||||||
chr1:56959801
|
A | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(87): Show | 122 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.249+219T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959801 | ||||||
chr1:56959881
|
G | A | 1 | a0001c0001t0001g0044 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.249+139C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959881 | ||||||
chr1:56960206
|
C | T | 16 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(13): Show | 18 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.93-30G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960206 | ||||||
chr1:56960215
|
AG | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0042others(29): Show | 41 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.93-40delC | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960215 | ||||||
chr1:56960225
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.93-49C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960225 | ||||||
chr1:56960344
|
T | TA | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG01175.hp2 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-169dupT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960344 | ||||||
chr1:56960409
|
T | C | 1 | a0004c0011t0001g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.93-233A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960409 | ||||||
chr1:56960434
|
A | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0266 | 3 | HG02056.hp1 NA18612.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.93-258T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960434 | ||||||
chr1:56960471
|
A | G | 19 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(16): Show | 21 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.93-295T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960471 | ||||||
chr1:56960492
|
C | T | 2 | a0001c0005t0001g0142a0001c0005t0001g0143 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-316G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960492 | ||||||
chr1:56960585
|
G | C | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.93-409C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960585 | ||||||
chr1:56960624
|
G | C | 1 | a0001c0001t0002g0030 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.93-448C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960624 | ||||||
chr1:56960720
|
A | T | 1 | a0001c0004t0001g0160 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.93-544T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960720 | ||||||
chr1:56960781
|
T | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(85): Show | 120 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.93-605A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960781 | ||||||
chr1:56960849
|
G | C | 2 | a0001c0005t0001g0142a0001c0005t0001g0143 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-673C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960849 | ||||||
chr1:56960856
|
G | A | 2 | a0001c0005t0001g0142a0001c0005t0001g0143 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-680C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960856 | ||||||
chr1:56960897
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0298a0001c0001t0001g0299 | 4 | HG02257.hp2 HG02280.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-721C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960897 | ||||||
chr1:56961029
|
G | T | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.93-853C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961029 | ||||||
chr1:56961120
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.93-944C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961120 | ||||||
chr1:56961208
|
A | T | 2 | a0001c0005t0001g0142a0001c0005t0001g0143 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-1032T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961208 | ||||||
chr1:56961224
|
T | G | 6 | a0001c0001t0001g0179a0001c0001t0001g0214a0001c0001t0001g0265others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-1048A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961224 | ||||||
chr1:56961277
|
T | C | 7 | a0002c0002t0001g0051a0002c0002t0001g0184a0002c0002t0001g0233others(4): Show | 8 | HG01070.hp1 HG01192.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.93-1101A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961277 | ||||||
chr1:56961298
|
G | A | 2 | a0001c0005t0001g0142a0001c0005t0001g0143 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-1122C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961298 | ||||||
chr1:56961412
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.93-1236G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961412 | ||||||
chr1:56961438
|
C | T | 9 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0064others(6): Show | 11 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-1262G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961438 | ||||||
chr1:56961450
|
G | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(16): Show | 21 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.93-1274C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961450 | ||||||
chr1:56961462
|
G | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(16): Show | 21 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.93-1286C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961462 | ||||||
chr1:56961547
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0092 | 3 | NA18946.hp2 NA18955.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.93-1371G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961547 | ||||||
chr1:56961573
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.93-1397G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961573 | ||||||
chr1:56961578
|
C | A | 30 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0064others(27): Show | 34 | HG00597.hp1 HG00639.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.93-1402G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961578 | ||||||
chr1:56961591
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.93-1415A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961591 | ||||||
chr1:56961628
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0139 | 5 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.93-1452A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961628 | ||||||
chr1:56961663
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.93-1487G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961663 | ||||||
chr1:56961768
|
G | A | 13 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-1592C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961768 | ||||||
chr1:56961788
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.93-1612G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961788 | ||||||
chr1:56961793
|
A | C | 19 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(16): Show | 21 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.93-1617T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961793 | ||||||
chr1:56961830
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(49): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.93-1654C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961830 | ||||||
chr1:56961885
|
G | A | 13 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-1709C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961885 | ||||||
chr1:56961971
|
T | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(9): Show | 14 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.93-1795A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961971 | ||||||
chr1:56962060
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.93-1884T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962060 | ||||||
chr1:56962174
|
T | G | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.93-1998A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962174 | ||||||
chr1:56962186
|
A | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 12 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.93-2010T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962186 | ||||||
chr1:56962187
|
G | T | 4 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077others(1): Show | 4 | HG02027.hp2 NA18939.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-2011C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962187 | ||||||
chr1:56962496
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.93-2320G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962496 | ||||||
chr1:56962708
|
A | G | 97 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(94): Show | 129 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.93-2532T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962708 | ||||||
chr1:56962730
|
G | A | 2 | a0001c0005t0001g0142a0001c0005t0001g0143 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-2554C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962730 | ||||||
chr1:56962759
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0002g0154 | 2 | HG00639.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.93-2583C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962759 | ||||||
chr1:56962916
|
T | C | 90 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(87): Show | 120 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.93-2740A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962916 | ||||||
chr1:56963007
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(119): Show | 166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.93-2831A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963007 | ||||||
chr1:56963047
|
T | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.92+2810A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963047 | ||||||
chr1:56963193
|
C | T | 92 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(89): Show | 123 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.92+2664G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963193 | ||||||
chr1:56963214
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(52): Show | 68 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.92+2643C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963214 | ||||||
chr1:56963221
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.92+2636T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963221 | ||||||
chr1:56963299
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.92+2558C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963299 | ||||||
chr1:56963449
|
A | G | 1 | a0001c0001t0002g0261 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.92+2408T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963449 | ||||||
chr1:56963466
|
C | G | 1 | a0001c0001t0001g0260 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.92+2391G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963466 | ||||||
chr1:56963466
|
C | T | 1 | a0001c0001t0002g0050 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.92+2391G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963466 | ||||||
chr1:56963467
|
G | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(53): Show | 69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.92+2390C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963467 | ||||||
chr1:56963499
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(52): Show | 68 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.92+2358G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963499 | ||||||
chr1:56963531
|
T | C | 35 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0042others(32): Show | 44 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.92+2326A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963531 | ||||||
chr1:56963562
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.92+2295T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963562 | ||||||
chr1:56963575
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.92+2282T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963575 | ||||||
chr1:56963589
|
TG | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(94): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.92+2267delC | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963589 | ||||||
chr1:56963590
|
G | GGGGGTCA others(29): Show |
1 | a0001c0001t0001g0259 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.92+2266_92+2267ins others(36): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963590 | ||||||
chr1:56963596
|
T | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(137): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.92+2261A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963596 | ||||||
chr1:56963597
|
G | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(79): Show | 112 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.92+2260C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963597 | ||||||
chr1:56963651
|
A | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(142): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.92+2206T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963651 | ||||||
chr1:56963780
|
G | C | 1 | a0001c0001t0001g0229 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.92+2077C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963780 | ||||||
chr1:56963817
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.92+2040G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963817 | ||||||
chr1:56964274
|
A | T | 6 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(3): Show | 6 | HG01175.hp2 HG01255.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+1583T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964274 | ||||||
chr1:56964280
|
T | C | 1 | a0001c0001t0001g0007 | 4 | NA18942.hp1 NA18951.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+1577A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964280 | ||||||
chr1:56964286
|
C | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0096others(4): Show | 9 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.92+1571G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964286 | ||||||
chr1:56964365
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.92+1492G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964365 | ||||||
chr1:56964495
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92+1362G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964495 | ||||||
chr1:56964554
|
G | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0065others(8): Show | 13 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.92+1303C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964554 | ||||||
chr1:56964567
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 8 | HG02145.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.92+1290C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964567 | ||||||
chr1:56964629
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.92+1228A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964629 | ||||||
chr1:56964668
|
C | CT | 12 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0065others(9): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+1188_92+1189ins others(1): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964668 | ||||||
chr1:56964668
|
C | T | 1 | a0001c0001t0002g0252 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.92+1189G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964668 | ||||||
chr1:56964727
|
G | A | 1 | a0004c0011t0001g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.92+1130C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964727 | ||||||
chr1:56964869
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.92+988G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964869 | ||||||
chr1:56964885
|
G | C | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92+972C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964885 | ||||||
chr1:56964910
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0228 | 4 | HG01069.hp2 HG01071.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+947G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964910 | ||||||
chr1:56964973
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.92+884A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964973 | ||||||
chr1:56965132
|
C | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(80): Show | 121 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.92+725G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965132 | ||||||
chr1:56965162
|
C | G | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92+695G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965162 | ||||||
chr1:56965175
|
A | T | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92+682T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965175 | ||||||
chr1:56965213
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(96): Show | 139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.92+644G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965213 | ||||||
chr1:56965222
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.92+635G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965222 | ||||||
chr1:56965311
|
G | A | 27 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0065others(24): Show | 30 | HG00597.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.92+546C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965311 | ||||||
chr1:56965332
|
T | C | 1 | a0001c0001t0002g0251 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.92+525A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965332 | ||||||
chr1:56965378
|
T | TGAGA | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(60): Show | 95 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.92+475_92+478dupTC others(2): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965378 | ||||||
chr1:56965392
|
A | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0098others(6): Show | 14 | HG01069.hp1 HG01978.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+465T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965392 | ||||||
chr1:56965394
|
A | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0098others(6): Show | 14 | HG01069.hp1 HG01978.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+463T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965394 | ||||||
chr1:56965396
|
A | AGT | 7 | a0001c0001t0001g0159a0001c0001t0002g0061a0001c0001t0002g0062others(4): Show | 9 | HG01070.hp1 HG01109.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+460_92+461insAC | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965396 | ||||||
chr1:56965396
|
A | AGTGTGTG others(1): Show |
2 | a0001c0001t0001g0019a0001c0001t0002g0090 | 3 | HG02896.hp1 HG02897.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.92+460_92+461insAC others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965396 | ||||||
chr1:56965396
|
A | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0098others(6): Show | 14 | HG01069.hp1 HG01978.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+461T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965396 | ||||||
chr1:56965398
|
A | AGAGAGT | 8 | a0001c0001t0001g0048a0001c0001t0001g0218a0001c0001t0001g0220others(5): Show | 11 | HG00280.hp1 HG00438.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(4): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGAGTG others(1): Show |
2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 4 | HG01346.hp1 HG01978.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGAGTG others(3): Show |
2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02630.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.92+458_92+459insAC others(8): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGAGTG others(5): Show |
1 | a0001c0001t0001g0156 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.92+458_92+459insAC others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGAGTG others(7): Show |
2 | a0001c0001t0001g0097a0001c0001t0002g0020 | 3 | HG00738.hp2 HG01261.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.92+458_92+459insAC others(12): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGAGTG others(9): Show |
1 | a0001c0001t0001g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.92+458_92+459insAC others(14): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGAGTG others(11): Show |
7 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0085others(4): Show | 7 | HG00597.hp1 HG00735.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(16): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGAGTG others(13): Show |
2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | HG02027.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.92+458_92+459insAC others(18): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGAGTG others(15): Show |
2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | NA18939.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.92+458_92+459insAC others(20): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGT | 6 | a0001c0001t0001g0045a0001c0001t0001g0071a0001c0001t0001g0214others(3): Show | 7 | HG01109.hp1 HG01346.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(2): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGTGT | 11 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0065others(8): Show | 13 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(4): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGTGTG others(3): Show |
7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0151others(4): Show | 9 | HG00639.hp2 HG02300.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(8): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGTGTG others(5): Show |
1 | a0001c0001t0001g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92+458_92+459insAC others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGAGTGTG others(7): Show |
1 | a0001c0001t0001g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.92+458_92+459insAC others(12): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGT | 40 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0042others(37): Show | 49 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.92+457_92+458dupAC | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGTGT | 22 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0167others(19): Show | 30 | HG00544.hp1 HG00673.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.92+455_92+458dupAC others(2): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGTGTGTG others(1): Show |
62 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0024others(59): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.92+451_92+458dupAC others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGTGTGTG others(3): Show |
5 | a0001c0001t0001g0092a0001c0001t0002g0091a0001c0001t0002g0093others(2): Show | 5 | HG01884.hp1 HG01934.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+449_92+458dupAC others(8): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | AGTGTGTG others(5): Show |
2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG02970.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.92+447_92+458dupAC others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965398
|
A | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0022others(15): Show | 26 | HG01069.hp1 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.92+459T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | ||||||
chr1:56965400
|
T | A | 2 | a0001c0001t0002g0302a0002c0002t0001g0301 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.92+457A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965400 | ||||||
chr1:56965512
|
TTCATGAA others(12): Show |
T | 11 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0065others(8): Show | 13 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.92+326_92+344delCA others(17): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965512 | ||||||
chr1:56965578
|
G | A | 4 | a0001c0001t0002g0061a0001c0001t0002g0062a0002c0002t0001g0304others(1): Show | 6 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+279C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965578 | ||||||
chr1:56965589
|
G | T | 1 | a0001c0001t0002g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.92+268C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965589 | ||||||
chr1:56965702
|
A | G | 12 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0065others(9): Show | 14 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+155T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965702 | ||||||
chr1:56965805
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.92+52G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965805 |