geneid | 9789 |
---|---|
ensemblid | ENSG00000118363.13 |
hgncid | 28962 |
symbol | SPCS2 |
name | signal peptidase complex subunit 2 |
refseq_nuc | NM_014752.3 |
refseq_prot | NP_055567.2 |
ensembl_nuc | ENST00000263672.11 |
ensembl_prot | ENSP00000263672.6 |
mane_status | MANE Select |
chr | chr11 |
start | 74949266 |
end | 74979033 |
strand | + |
ver | v1.2 |
region | chr11:74949266-74979033 |
region5000 | chr11:74944266-74984033 |
regionname0 | SPCS2_chr11_74949266_74979033 |
regionname5000 | SPCS2_chr11_74944266_74984033 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 226 | 378 | 98 | 60 | 158 | 18 | 42 | 126 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2011 | 219 | 61 | 28 | 101 | 10 | 18 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0002 | 0/0 | 2011 | 105 | 24 | 20 | 40 | 6 | 15 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0003 | 0/0 | 2011 | 11 | 0 | 6 | 0 | 1 | 4 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0004 | 0/0 | 2008 | 10 | 0 | 1 | 9 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0005 | 0/1 | 2011 | 9 | 0 | 4 | 0 | 1 | 3 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0006 | 0/0 | 2011 | 9 | 9 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0007 | 0/0 | 2012 | 4 | 0 | 0 | 4 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0008 | 0/0 | 2011 | 3 | 3 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0009 | 0/0 | 2011 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0010 | 0/0 | 2011 | 2 | 0 | 0 | 0 | 0 | 2 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0011 | 0/0 | 2011 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0012 | 0/0 | 2011 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0013 | 0/0 | 2011 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
t0014 | 0/0 | 2011 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 1 | 4 | 4 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0002 | 0/0 | 7 | 0 | 2 | 3 | 0 | 2 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0007 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0010 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0011 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0015 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0024 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0042 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 681 | 367 | 87 | 60 | 158 | 18 | 42 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0002 | 0/0 | 681 | 11 | 11 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2691 | 208 | 50 | 28 | 101 | 10 | 18 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0002 | 0/0 | 2691 | 105 | 24 | 20 | 40 | 6 | 15 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0003 | 0/0 | 2691 | 11 | 0 | 6 | 0 | 1 | 4 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0004 | 0/0 | 2688 | 10 | 0 | 1 | 9 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0005 | 0/1 | 2691 | 9 | 0 | 4 | 0 | 1 | 3 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0006 | 0/0 | 2691 | 9 | 9 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0007 | 0/0 | 2692 | 4 | 0 | 0 | 4 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0008 | 0/0 | 2691 | 3 | 3 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0009 | 0/0 | 2691 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0010 | 0/0 | 2691 | 2 | 0 | 0 | 0 | 0 | 2 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0011 | 0/0 | 2691 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0012 | 0/0 | 2691 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0013 | 0/0 | 2691 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0001t0014 | 0/0 | 2691 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
a0001c0002t0001 | 0/0 | 2691 | 11 | 11 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | copy fasta | chr11 | 74944266 | 74984033 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0018 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0042 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0005g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0005g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0005g0024 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0009g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0009g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0010g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0010g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0011g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0012g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0013g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0232 | EUR | GBR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0001 | EUR | GBR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0240 | EUR | GBR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0255 | EUR | FIN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0238 | EUR | FIN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00408 | hp1 | a0001 | c0001 | t0012 | g0034 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01071 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0221 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01884 | hp2 | a0001 | c0001 | t0014 | g0144 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0065 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CDX | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02155 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | CDX | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | CDX | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0284 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0064 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02683 | hp2 | a0001 | c0001 | t0010 | g0247 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0286 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0282 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0285 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0063 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03239 | hp2 | a0001 | c0001 | t0010 | g0250 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0179 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0002 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0027 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0074 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18965 | hp2 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18984 | hp1 | a0001 | c0001 | t0013 | g0213 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18993 | hp1 | a0001 | c0001 | t0007 | g0097 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19010 | hp1 | a0001 | c0001 | t0009 | g0083 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19064 | hp1 | a0001 | c0001 | t0009 | g0029 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19090 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | ASW | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ASW | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0099 | EUR | TSI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | GIH | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | GIH | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | USA | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | USA | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0024 | REF | REF | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0131 | REF | REF | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74976995
|
A | G | 1 | a0001c0002 | 11 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(8): Show |
synonymous_variant | LOW | c.633A>G | p.Glu211Glu | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 653/2691 | 633/681 | 211/226 | chr11 | 74976995 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74977098
|
G | C | 1 | a0001c0001t0009 | 2 | NA19010.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*55G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 55 | chr11 | 74977098 | |||||
chr11:74977590
|
A | G | 1 | a0001c0001t0014 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 547 | chr11 | 74977590 | |||||
chr11:74977658
|
A | G | 1 | a0001c0001t0013 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*615A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 615 | chr11 | 74977658 | |||||
chr11:74977888
|
CAAT | C | 1 | a0001c0001t0004 | 10 | HG02148.hp2 NA18945.hp1 NA18946.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*851_*853delTAA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 851 | INFO_REALIGN_3_PRIME | chr11 | 74977888 | ||||
chr11:74978013
|
A | C | 1 | a0001c0001t0006 | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*970A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 970 | chr11 | 74978013 | |||||
chr11:74978313
|
A | G | 1 | a0001c0001t0010 | 2 | HG02683.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1270A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1270 | chr11 | 74978313 | |||||
chr11:74978327
|
G | A | 5 | a0001c0001t0002a0001c0001t0006a0001c0001t0010others(2): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1284G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1284 | chr11 | 74978327 | |||||
chr11:74978376
|
T | C | 1 | a0001c0001t0011 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1333T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1333 | chr11 | 74978376 | |||||
chr11:74978485
|
T | TA | 1 | a0001c0001t0007 | 4 | HG02155.hp2 NA18965.hp2 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1443dupA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1444 | INFO_REALIGN_3_PRIME | chr11 | 74978485 | ||||
chr11:74978580
|
C | T | 1 | a0001c0001t0008 | 3 | HG02145.hp1 HG02615.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1537C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1537 | chr11 | 74978580 | |||||
chr11:74978605
|
C | G | 1 | a0001c0001t0003 | 11 | HG01099.hp1 HG01106.hp1 HG01109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1562C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1562 | chr11 | 74978605 | |||||
chr11:74978936
|
T | C | 1 | a0001c0001t0005 | 9 | HG00099.hp2 HG00642.hp2 HG01167.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1893T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1893 | chr11 | 74978936 | |||||
chr11:74979011
|
A | G | 1 | a0001c0001t0012 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1968A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1968 | chr11 | 74979011 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74949459
|
A | C | 92 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(89): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.114+60A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949459 | ||||||
chr11:74949488
|
C | A | 1 | a0001c0001t0013g0213 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.114+89C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949488 | ||||||
chr11:74949505
|
G | C | 1 | a0001c0001t0002g0214 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.114+106G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949505 | ||||||
chr11:74949540
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.114+141C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949540 | ||||||
chr11:74949541
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.114+142G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949541 | ||||||
chr11:74949586
|
G | A | 73 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(70): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.114+187G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949586 | ||||||
chr11:74949622
|
T | A | 1 | a0001c0001t0001g0047 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.114+223T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949622 | ||||||
chr11:74949673
|
A | C | 5 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0288others(2): Show | 7 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+274A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949673 | ||||||
chr11:74949705
|
G | A | 12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0002t0001g0023others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+306G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949705 | ||||||
chr11:74949776
|
C | G | 37 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(34): Show | 46 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.114+377C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949776 | ||||||
chr11:74949806
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.114+407G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949806 | ||||||
chr11:74949973
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.114+574C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949973 | ||||||
chr11:74950039
|
T | G | 2 | a0001c0001t0002g0215a0001c0001t0002g0216 | 2 | HG01433.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.114+640T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950039 | ||||||
chr11:74950057
|
C | A | 1 | a0001c0001t0002g0217 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.114+658C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950057 | ||||||
chr11:74950065
|
T | A | 92 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(89): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.114+666T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950065 | ||||||
chr11:74950086
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114+687G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950086 | ||||||
chr11:74950190
|
C | T | 73 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(70): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.114+791C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950190 | ||||||
chr11:74950295
|
A | G | 7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0282others(4): Show | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+896A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950295 | ||||||
chr11:74950611
|
A | G | 3 | a0001c0001t0003g0177a0001c0001t0003g0178a0001c0001t0003g0179 | 3 | HG01109.hp1 HG01496.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.114+1212A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950611 | ||||||
chr11:74950641
|
A | G | 7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0282others(4): Show | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+1242A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950641 | ||||||
chr11:74950659
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.114+1260C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950659 | ||||||
chr11:74950667
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.114+1268G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950667 | ||||||
chr11:74950890
|
G | T | 81 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.114+1491G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950890 | ||||||
chr11:74950984
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.114+1585T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950984 | ||||||
chr11:74950993
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0176 | 3 | NA18974.hp2 NA18978.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.114+1594C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950993 | ||||||
chr11:74951000
|
G | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0175 | 4 | HG00639.hp2 HG01074.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1601G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951000 | ||||||
chr11:74951023
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.114+1624T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951023 | ||||||
chr11:74951063
|
G | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0172others(2): Show | 11 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+1664G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951063 | ||||||
chr11:74951099
|
G | T | 1 | a0001c0001t0002g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.114+1700G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951099 | ||||||
chr11:74951109
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.114+1710A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951109 | ||||||
chr11:74951146
|
G | A | 3 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0002g0278 | 3 | HG01884.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+1747G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951146 | ||||||
chr11:74951209
|
A | G | 8 | a0001c0001t0002g0004a0001c0001t0002g0021a0001c0001t0002g0217others(5): Show | 15 | HG00673.hp2 NA18941.hp2 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.114+1810A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951209 | ||||||
chr11:74951228
|
A | C | 2 | a0001c0001t0002g0268a0001c0001t0002g0269 | 2 | HG01106.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.114+1829A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951228 | ||||||
chr11:74951304
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0172others(2): Show | 11 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+1905A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951304 | ||||||
chr11:74951322
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.114+1923G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951322 | ||||||
chr11:74951446
|
G | A | 8 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0276others(5): Show | 9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+2047G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951446 | ||||||
chr11:74951475
|
A | G | 12 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0288others(9): Show | 16 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+2076A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951475 | ||||||
chr11:74951536
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.114+2137C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951536 | ||||||
chr11:74951703
|
G | A | 3 | a0001c0001t0008g0063a0001c0001t0008g0064a0001c0001t0008g0065 | 3 | HG02145.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.114+2304G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951703 | ||||||
chr11:74951759
|
G | A | 12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0002t0001g0023others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+2360G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951759 | ||||||
chr11:74951767
|
G | A | 3 | a0001c0001t0002g0016a0001c0001t0002g0219a0001c0001t0002g0220 | 5 | HG01168.hp2 HG01169.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+2368G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951767 | ||||||
chr11:74951773
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.114+2374G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951773 | ||||||
chr11:74951810
|
C | CA | 7 | a0001c0001t0001g0038a0001c0001t0001g0066a0001c0001t0001g0172others(4): Show | 8 | HG00639.hp2 HG02165.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2430dupA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | |||||
chr11:74951810
|
C | CAAAAAA | 8 | a0001c0001t0002g0022a0001c0001t0002g0220a0001c0001t0002g0265others(5): Show | 10 | HG01169.hp2 HG01255.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.114+2425_114+2430d others(8): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | |||||
chr11:74951810
|
C | CAAAAAAA | 60 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(57): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.114+2424_114+2430d others(9): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | |||||
chr11:74951810
|
C | CAAAAAAA others(1): Show |
14 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0222others(11): Show | 15 | HG00735.hp1 HG00735.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+2423_114+2430d others(10): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | |||||
chr11:74951810
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0282others(4): Show | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+2422_114+2430d others(11): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | |||||
chr11:74951810
|
CA | C | 19 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(16): Show | 20 | HG00323.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+2430delA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | |||||
chr11:74951928
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.114+2529G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951928 | ||||||
chr11:74951984
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.114+2585A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951984 | ||||||
chr11:74952283
|
C | T | 3 | a0001c0001t0008g0063a0001c0001t0008g0064a0001c0001t0008g0065 | 3 | HG02145.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.114+2884C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952283 | ||||||
chr11:74952443
|
GT | G | 8 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0276others(5): Show | 9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+3050delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74952443 | |||||
chr11:74952499
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.114+3100T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952499 | ||||||
chr11:74952507
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.114+3108A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952507 | ||||||
chr11:74952534
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0164 | 3 | NA18981.hp1 NA18988.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.114+3135C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952534 | ||||||
chr11:74952892
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.114+3493T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952892 | ||||||
chr11:74952916
|
TGA | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+3518_114+3519d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952916 | ||||||
chr11:74952919
|
C | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+3520C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952919 | ||||||
chr11:74952921
|
T | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+3522T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952921 | ||||||
chr11:74952922
|
A | G | 3 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+3523A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952922 | ||||||
chr11:74952980
|
G | A | 93 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(90): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.114+3581G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952980 | ||||||
chr11:74953083
|
C | G | 1 | a0001c0001t0002g0264 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.114+3684C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953083 | ||||||
chr11:74953217
|
A | ATT | 5 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0284others(2): Show | 7 | HG02451.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.114+3832_114+3833d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74953217 | |||||
chr11:74953217
|
AT | A | 20 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0071others(17): Show | 21 | HG00408.hp2 HG01069.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.114+3833delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74953217 | |||||
chr11:74953256
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.114+3857A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953256 | ||||||
chr11:74953257
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.114+3858A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953257 | ||||||
chr11:74953274
|
C | T | 1 | a0001c0001t0013g0213 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.114+3875C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953274 | ||||||
chr11:74953287
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.114+3888G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953287 | ||||||
chr11:74953459
|
C | T | 9 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0155others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+4060C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953459 | ||||||
chr11:74953476
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.114+4077C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953476 | ||||||
chr11:74953681
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.114+4282T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953681 | ||||||
chr11:74953856
|
A | T | 2 | a0001c0001t0006g0282a0001c0001t0006g0283 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.114+4457A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953856 | ||||||
chr11:74953938
|
G | C | 2 | a0001c0001t0002g0222a0001c0001t0002g0228 | 2 | HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.114+4539G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953938 | ||||||
chr11:74954271
|
G | A | 12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0002t0001g0023others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+4872G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954271 | ||||||
chr11:74954397
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.114+4998G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954397 | ||||||
chr11:74954657
|
G | C | 1 | a0001c0001t0002g0215 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.114+5258G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954657 | ||||||
chr11:74954699
|
C | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+5300C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954699 | ||||||
chr11:74954700
|
G | A | 1 | a0001c0001t0003g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114+5301G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954700 | ||||||
chr11:74954704
|
C | T | 2 | a0001c0001t0002g0288a0001c0001t0002g0290 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.114+5305C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954704 | ||||||
chr11:74954895
|
T | A | 1 | a0001c0001t0002g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.114+5496T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954895 | ||||||
chr11:74954943
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.114+5544C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954943 | ||||||
chr11:74955047
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+5648A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955047 | ||||||
chr11:74955060
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.114+5661A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955060 | ||||||
chr11:74955387
|
C | T | 8 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0276others(5): Show | 9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+5988C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955387 | ||||||
chr11:74955440
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.114+6041G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955440 | ||||||
chr11:74955477
|
A | G | 3 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+6078A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955477 | ||||||
chr11:74955642
|
G | A | 8 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0276others(5): Show | 9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+6243G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955642 | ||||||
chr11:74955709
|
G | A | 8 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0276others(5): Show | 9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+6310G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955709 | ||||||
chr11:74955814
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.114+6415T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955814 | ||||||
chr11:74955851
|
A | AAT | 19 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(16): Show | 24 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.114+6487_114+6488d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATAT | 17 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0124others(14): Show | 17 | HG00408.hp2 HG00639.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.114+6485_114+6488d others(6): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATAT | 15 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+6483_114+6488d others(8): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(1): Show |
10 | a0001c0001t0001g0034a0001c0001t0001g0118a0001c0001t0001g0161others(7): Show | 10 | HG00408.hp1 HG01106.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+6481_114+6488d others(10): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(3): Show |
20 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0033others(17): Show | 25 | HG00140.hp1 HG00733.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.114+6479_114+6488d others(12): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(5): Show |
9 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(6): Show | 9 | HG00323.hp2 HG01243.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+6477_114+6488d others(14): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(7): Show |
5 | a0001c0001t0001g0012a0001c0001t0001g0041a0001c0001t0002g0234others(2): Show | 8 | HG00423.hp2 HG01069.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+6475_114+6488d others(16): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(9): Show |
5 | a0001c0001t0001g0031a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 6 | HG00140.hp2 HG01168.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+6473_114+6488d others(18): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(11): Show |
8 | a0001c0001t0001g0030a0001c0001t0001g0062a0001c0001t0001g0105others(5): Show | 9 | HG00323.hp1 HG01256.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+6471_114+6488d others(20): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(13): Show |
10 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0104others(7): Show | 11 | HG00099.hp1 HG00609.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+6469_114+6488d others(22): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(15): Show |
16 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(13): Show | 25 | HG00423.hp1 HG00733.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.114+6467_114+6488d others(24): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(17): Show |
17 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0039others(14): Show | 29 | HG00099.hp2 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.114+6465_114+6488d others(26): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(19): Show |
17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(14): Show | 24 | HG00609.hp1 HG01081.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.114+6463_114+6488d others(28): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(21): Show |
15 | a0001c0001t0001g0026a0001c0001t0001g0059a0001c0001t0001g0060others(12): Show | 18 | HG00280.hp2 HG01099.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.114+6461_114+6488d others(30): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(23): Show |
15 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0081others(12): Show | 18 | HG00642.hp2 HG01109.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.114+6459_114+6488d others(32): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(25): Show |
7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG00558.hp1 HG01081.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.114+6457_114+6488d others(34): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(27): Show |
2 | a0001c0001t0001g0075a0001c0001t0003g0074 | 2 | HG04184.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.114+6455_114+6488d others(36): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | AATATATA others(37): Show |
1 | a0001c0001t0001g0073 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.114+6488_114+6489i others(46): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0275 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.114+6452_114+6453i others(15): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | ||||||
chr11:74955851
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0002g0263 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.114+6452_114+6453i others(17): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | ||||||
chr11:74955851
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0184 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.114+6452_114+6453i others(21): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | ||||||
chr11:74955851
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0151 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.114+6452_114+6453i others(23): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | ||||||
chr11:74955851
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01952.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.114+6452_114+6453i others(25): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | ||||||
chr11:74955851
|
A | ATATATAT others(18): Show |
3 | a0001c0001t0001g0211a0001c0001t0006g0286a0001c0002t0001g0055 | 3 | HG01891.hp1 HG02723.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.114+6452_114+6453i others(27): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | ||||||
chr11:74955851
|
A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0148a0001c0001t0004g0147 | 2 | NA18975.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.114+6452_114+6453i others(29): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | ||||||
chr11:74955851
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0146 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.114+6452_114+6453i others(31): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | ||||||
chr11:74955851
|
A | T | 1 | a0001c0001t0001g0152 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.114+6452A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | ||||||
chr11:74955851
|
AAT | A | 6 | a0001c0001t0001g0067a0001c0001t0002g0020a0001c0001t0003g0179others(3): Show | 8 | HG02145.hp1 HG02615.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+6487_114+6488d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
AATAT | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0134a0001c0001t0002g0262others(1): Show | 4 | HG01243.hp2 HG03098.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+6485_114+6488d others(6): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
AATATAT | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 6 | HG02818.hp1 NA18966.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+6483_114+6488d others(8): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
AATATATA others(1): Show |
A | 9 | a0001c0001t0001g0137a0001c0001t0001g0209a0001c0001t0002g0004others(6): Show | 14 | HG00673.hp2 HG01981.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+6481_114+6488d others(10): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
AATATATA others(3): Show |
A | 3 | a0001c0001t0001g0138a0001c0001t0001g0172a0001c0001t0001g0210 | 3 | HG02080.hp1 HG02451.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.114+6479_114+6488d others(12): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
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AATATATA others(5): Show |
A | 5 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0139others(2): Show | 11 | HG02040.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+6477_114+6488d others(14): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
AATATATA others(7): Show |
A | 9 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0276others(6): Show | 10 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+6475_114+6488d others(16): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
AATATATA others(9): Show |
A | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.114+6473_114+6488d others(18): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
AATATATA others(11): Show |
A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0014g0144 | 3 | HG00544.hp1 HG01884.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.114+6471_114+6488d others(20): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
AATATATA others(13): Show |
A | 1 | a0001c0001t0001g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.114+6469_114+6488d others(22): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
AATATATA others(15): Show |
A | 6 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289others(3): Show | 8 | HG02258.hp1 HG02486.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+6467_114+6488d others(24): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955851
|
AATATATA others(21): Show |
A | 2 | a0001c0001t0002g0288a0001c0001t0002g0290 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.114+6461_114+6488d others(30): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | |||||
chr11:74955884
|
A | ATATATAT others(23): Show |
1 | a0001c0002t0001g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.114+6488_114+6489i others(32): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955884 | |||||
chr11:74955884
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0095 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.114+6488_114+6489i others(30): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955884 | |||||
chr11:74955884
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0101 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.114+6488_114+6489i others(28): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955884 | |||||
chr11:74955887
|
T | TATATATA others(21): Show |
1 | a0001c0001t0003g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.114+6488_114+6489i others(30): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955887 | ||||||
chr11:74955925
|
C | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+6526C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955925 | ||||||
chr11:74955965
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.114+6566A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955965 | ||||||
chr11:74956057
|
A | G | 3 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0002g0278 | 3 | HG01884.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+6658A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956057 | ||||||
chr11:74956221
|
A | G | 2 | a0001c0001t0002g0230a0001c0001t0002g0233 | 2 | HG01361.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.114+6822A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956221 | ||||||
chr11:74956536
|
A | AT | 24 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0057others(21): Show | 27 | HG00639.hp2 HG01074.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.114+7141dupT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74956536 | |||||
chr11:74956836
|
C | A | 8 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0276others(5): Show | 9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+7437C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956836 | ||||||
chr11:74956858
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.114+7459G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956858 | ||||||
chr11:74956950
|
A | G | 12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0002t0001g0023others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+7551A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956950 | ||||||
chr11:74956968
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.114+7569C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956968 | ||||||
chr11:74957028
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.114+7629C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957028 | ||||||
chr11:74957036
|
G | C | 93 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(90): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.114+7637G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957036 | ||||||
chr11:74957054
|
G | A | 9 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0155others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+7655G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957054 | ||||||
chr11:74957089
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.114+7690A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957089 | ||||||
chr11:74957611
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.115-7423A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957611 | ||||||
chr11:74957968
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.115-7066A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957968 | ||||||
chr11:74958015
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0210 | 2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.115-7019T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958015 | ||||||
chr11:74958129
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.115-6905C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958129 | ||||||
chr11:74958224
|
A | G | 4 | a0001c0001t0003g0088a0001c0001t0003g0100a0001c0001t0003g0119others(1): Show | 4 | HG01099.hp1 HG01106.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-6810A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958224 | ||||||
chr11:74958349
|
T | G | 73 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(70): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.115-6685T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958349 | ||||||
chr11:74958454
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0172others(2): Show | 11 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-6580G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958454 | ||||||
chr11:74958509
|
T | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0141 | 2 | HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-6525T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958509 | ||||||
chr11:74958605
|
A | G | 2 | a0001c0001t0002g0236a0001c0001t0002g0246 | 2 | HG01261.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.115-6429A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958605 | ||||||
chr11:74958981
|
T | G | 2 | a0001c0001t0002g0288a0001c0001t0002g0290 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.115-6053T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958981 | ||||||
chr11:74959084
|
C | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0067a0001c0001t0001g0068others(6): Show | 11 | HG00639.hp2 HG01074.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-5950C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959084 | ||||||
chr11:74959285
|
C | G | 1 | a0001c0001t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115-5749C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959285 | ||||||
chr11:74959366
|
G | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-5668G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959366 | ||||||
chr11:74959429
|
A | G | 7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0282others(4): Show | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-5605A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959429 | ||||||
chr11:74959457
|
A | G | 5 | a0001c0001t0001g0079a0001c0001t0001g0093a0001c0001t0001g0104others(2): Show | 5 | HG01884.hp2 NA18974.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-5577A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959457 | ||||||
chr11:74959461
|
C | T | 9 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0155others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-5573C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959461 | ||||||
chr11:74959640
|
C | T | 2 | a0001c0001t0006g0282a0001c0001t0006g0283 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.115-5394C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959640 | ||||||
chr11:74959741
|
G | A | 12 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0288others(9): Show | 16 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.115-5293G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959741 | ||||||
chr11:74959766
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.115-5268G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959766 | ||||||
chr11:74959814
|
A | G | 12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0002t0001g0023others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.115-5220A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959814 | ||||||
chr11:74960055
|
T | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(77): Show | 101 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.115-4979T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960055 | ||||||
chr11:74960289
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.115-4745G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960289 | ||||||
chr11:74960312
|
C | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0075a0001c0001t0001g0092others(2): Show | 6 | NA18612.hp1 NA18954.hp2 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-4722C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960312 | ||||||
chr11:74960313
|
A | G | 1 | a0001c0001t0002g0239 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-4721A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960313 | ||||||
chr11:74960440
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.115-4594G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960440 | ||||||
chr11:74960440
|
G | C | 1 | a0001c0001t0001g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.115-4594G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960440 | ||||||
chr11:74960441
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.115-4593G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960441 | ||||||
chr11:74960502
|
C | CT | 81 | a0001c0001t0001g0102a0001c0001t0002g0004a0001c0001t0002g0008others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.115-4518dupT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74960502 | |||||
chr11:74960523
|
TTA | T | 8 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0276others(5): Show | 9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-4510_115-4509d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960523 | ||||||
chr11:74960601
|
G | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0098a0001c0001t0001g0122others(2): Show | 6 | HG01981.hp2 NA18970.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-4433G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960601 | ||||||
chr11:74960604
|
C | CT | 93 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(90): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.115-4427dupT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74960604 | |||||
chr11:74960677
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0172 | 3 | HG02258.hp2 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.115-4357A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960677 | ||||||
chr11:74960868
|
T | A | 12 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0288others(9): Show | 16 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.115-4166T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960868 | ||||||
chr11:74960891
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115-4143T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960891 | ||||||
chr11:74961035
|
TA | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0112others(8): Show | 17 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.115-3985delA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74961035 | |||||
chr11:74961079
|
C | G | 1 | a0001c0001t0002g0226 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.115-3955C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961079 | ||||||
chr11:74961123
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.115-3911A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961123 | ||||||
chr11:74961240
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0289 | 4 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-3794G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961240 | ||||||
chr11:74961494
|
G | A | 7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0282others(4): Show | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-3540G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961494 | ||||||
chr11:74961517
|
T | G | 1 | a0001c0001t0001g0193 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.115-3517T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961517 | ||||||
chr11:74961517
|
TTTG | T | 11 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0155others(8): Show | 12 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.115-3502_115-3500d others(5): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74961517 | |||||
chr11:74961529
|
GTTGT | G | 4 | a0001c0001t0001g0057a0001c0001t0001g0189a0001c0001t0002g0288others(1): Show | 4 | HG00558.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-3482_115-3479d others(6): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74961529 | |||||
chr11:74961574
|
TCTGTTCA others(42): Show |
T | 1 | a0001c0001t0002g0221 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.115-3457_115-3409d others(51): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74961574 | |||||
chr11:74961593
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.115-3441G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961593 | ||||||
chr11:74961726
|
C | T | 1 | a0001c0001t0002g0271 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.115-3308C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961726 | ||||||
chr11:74961734
|
G | A | 9 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0155others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-3300G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961734 | ||||||
chr11:74961765
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(205): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.115-3269T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961765 | ||||||
chr11:74962131
|
T | C | 1 | a0001c0001t0010g0247 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.115-2903T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962131 | ||||||
chr11:74962225
|
A | G | 81 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.115-2809A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962225 | ||||||
chr11:74962395
|
C | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0001g0136 | 3 | HG02818.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.115-2639C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962395 | ||||||
chr11:74962396
|
T | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0001g0136 | 3 | HG02818.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.115-2638T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962396 | ||||||
chr11:74962548
|
CA | C | 79 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0061others(76): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.115-2472delA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74962548 | |||||
chr11:74962579
|
C | G | 1 | a0001c0001t0002g0232 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.115-2455C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962579 | ||||||
chr11:74962582
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.115-2452G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962582 | ||||||
chr11:74962710
|
T | C | 1 | a0001c0001t0002g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-2324T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962710 | ||||||
chr11:74963253
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00544.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.115-1781A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963253 | ||||||
chr11:74963544
|
ATTGT | A | 4 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289others(1): Show | 6 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-1467_115-1464d others(6): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74963544 | |||||
chr11:74963567
|
G | A | 7 | a0001c0002t0001g0023a0001c0002t0001g0048a0001c0002t0001g0049others(4): Show | 8 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-1467G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963567 | ||||||
chr11:74963567
|
GTTTA | G | 33 | a0001c0001t0001g0046a0001c0001t0001g0082a0001c0001t0001g0098others(30): Show | 36 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.115-1447_115-1444d others(6): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74963567 | |||||
chr11:74963571
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(140): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.115-1463A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963571 | ||||||
chr11:74963575
|
A | G | 11 | a0001c0001t0001g0111a0001c0001t0002g0043a0001c0001t0002g0181others(8): Show | 12 | HG01099.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.115-1459A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963575 | ||||||
chr11:74963610
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.115-1424A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963610 | ||||||
chr11:74963907
|
A | G | 1 | a0001c0001t0002g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-1127A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963907 | ||||||
chr11:74964037
|
G | A | 1 | a0001c0001t0003g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.115-997G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74964037 | ||||||
chr11:74964787
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.115-247G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74964787 | ||||||
chr11:74964822
|
T | G | 8 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0276others(5): Show | 9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-212T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74964822 | ||||||
chr11:74964851
|
T | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(77): Show | 101 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.115-183T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74964851 | ||||||
chr11:74964986
|
G | A | 3 | a0001c0001t0008g0063a0001c0001t0008g0064a0001c0001t0008g0065 | 3 | HG02145.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.115-48G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74964986 | ||||||
chr11:74965306
|
A | G | 9 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0155others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.198+189A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965306 | ||||||
chr11:74965358
|
A | G | 1 | a0001c0001t0014g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.198+241A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965358 | ||||||
chr11:74965374
|
A | C | 81 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.198+257A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965374 | ||||||
chr11:74965467
|
G | T | 93 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(90): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.199-296G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965467 | ||||||
chr11:74965503
|
T | C | 1 | a0001c0001t0014g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.199-260T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965503 | ||||||
chr11:74965749
|
G | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.199-14G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965749 | ||||||
chr11:74965962
|
A | G | 1 | a0001c0001t0003g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.359+39A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74965962 | ||||||
chr11:74966191
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.359+268G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966191 | ||||||
chr11:74966203
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.359+280G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966203 | ||||||
chr11:74966394
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.359+471T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966394 | ||||||
chr11:74966415
|
T | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.359+492T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966415 | ||||||
chr11:74966495
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.359+572G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966495 | ||||||
chr11:74966773
|
C | CG | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.359+850_359+851ins others(1): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966773 | ||||||
chr11:74966773
|
C | CGT | 5 | a0001c0001t0001g0071a0001c0001t0001g0079a0001c0001t0001g0164others(2): Show | 5 | NA18946.hp2 NA18949.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.359+850_359+851ins others(2): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966773 | ||||||
chr11:74966846
|
G | A | 4 | a0001c0001t0002g0248a0001c0001t0002g0254a0001c0001t0002g0259others(1): Show | 4 | HG00544.hp2 HG02027.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+923G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966846 | ||||||
chr11:74966957
|
G | A | 7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0282others(4): Show | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.359+1034G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966957 | ||||||
chr11:74967044
|
A | T | 1 | a0001c0001t0002g0281 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.359+1121A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967044 | ||||||
chr11:74967134
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.359+1211G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967134 | ||||||
chr11:74967157
|
T | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.359+1234T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967157 | ||||||
chr11:74967158
|
T | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.359+1235T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967158 | ||||||
chr11:74967189
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.359+1266C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967189 | ||||||
chr11:74967437
|
T | TA | 93 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(90): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.359+1514_359+1515i others(3): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967437 | ||||||
chr11:74967479
|
G | A | 2 | a0001c0001t0002g0288a0001c0001t0002g0290 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.359+1556G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967479 | ||||||
chr11:74967529
|
C | T | 12 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0067others(9): Show | 14 | HG00639.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.359+1606C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967529 | ||||||
chr11:74967530
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.359+1607A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967530 | ||||||
chr11:74967592
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.359+1669T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967592 | ||||||
chr11:74967679
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.359+1756G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967679 | ||||||
chr11:74967680
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.359+1757C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967680 | ||||||
chr11:74967747
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.360-1818C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967747 | ||||||
chr11:74968010
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.360-1555T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968010 | ||||||
chr11:74968033
|
G | A | 2 | a0001c0001t0008g0063a0001c0001t0008g0065 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.360-1532G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968033 | ||||||
chr11:74968138
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0075a0001c0001t0001g0092others(2): Show | 6 | NA18612.hp1 NA18954.hp2 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.360-1427C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968138 | ||||||
chr11:74968258
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.360-1307T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968258 | ||||||
chr11:74968276
|
G | A | 67 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(64): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.360-1289G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968276 | ||||||
chr11:74968385
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.360-1180G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968385 | ||||||
chr11:74968435
|
C | G | 12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0002t0001g0023others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.360-1130C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968435 | ||||||
chr11:74968446
|
C | G | 1 | a0001c0001t0006g0283 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.360-1119C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968446 | ||||||
chr11:74968518
|
G | GT | 24 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0068others(21): Show | 25 | HG00544.hp2 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.360-1032dupT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 74968518 | |||||
chr11:74968518
|
GT | G | 23 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0022others(20): Show | 27 | HG01099.hp2 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.360-1032delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 74968518 | |||||
chr11:74968523
|
T | G | 2 | a0001c0002t0001g0048a0001c0002t0001g0049 | 2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.360-1042T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968523 | ||||||
chr11:74968578
|
C | T | 81 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.360-987C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968578 | ||||||
chr11:74968714
|
G | C | 2 | a0001c0001t0006g0282a0001c0001t0006g0283 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.360-851G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968714 | ||||||
chr11:74968816
|
C | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.360-749C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968816 | ||||||
chr11:74969137
|
A | G | 1 | a0001c0001t0007g0097 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.360-428A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74969137 | ||||||
chr11:74969755
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.494+56T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74969755 | ||||||
chr11:74969836
|
T | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0176 | 3 | NA18974.hp2 NA18978.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.494+137T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74969836 | ||||||
chr11:74969945
|
A | G | 7 | a0001c0002t0001g0023a0001c0002t0001g0048a0001c0002t0001g0049others(4): Show | 8 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.494+246A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74969945 | ||||||
chr11:74970061
|
A | G | 35 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 44 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.494+362A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970061 | ||||||
chr11:74970226
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494+527C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970226 | ||||||
chr11:74970345
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.494+646A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970345 | ||||||
chr11:74970364
|
A | G | 81 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.494+665A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970364 | ||||||
chr11:74970645
|
C | T | 9 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0155others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.494+946C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970645 | ||||||
chr11:74970802
|
C | T | 8 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0276others(5): Show | 9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.494+1103C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970802 | ||||||
chr11:74970873
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0001g0136 | 3 | HG02818.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.494+1174A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970873 | ||||||
chr11:74970908
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.494+1209A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970908 | ||||||
chr11:74970984
|
A | T | 1 | a0001c0001t0002g0238 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.494+1285A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970984 | ||||||
chr11:74971085
|
T | G | 6 | a0001c0001t0002g0215a0001c0001t0002g0216a0001c0001t0002g0234others(3): Show | 6 | HG00323.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.494+1386T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971085 | ||||||
chr11:74971159
|
G | A | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(298): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.494+1460G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971159 | ||||||
chr11:74971200
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.494+1501A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971200 | ||||||
chr11:74971441
|
C | A | 9 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0155others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.494+1742C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971441 | ||||||
chr11:74971583
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.494+1884C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971583 | ||||||
chr11:74971617
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.494+1918A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971617 | ||||||
chr11:74971749
|
A | G | 5 | a0001c0001t0002g0239a0001c0001t0002g0242a0001c0001t0002g0251others(2): Show | 5 | HG02615.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+2050A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971749 | ||||||
chr11:74971749
|
AT | A | 5 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0288others(2): Show | 7 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.494+2054delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74971749 | |||||
chr11:74971801
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.494+2102T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971801 | ||||||
chr11:74972113
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0117 | 2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.494+2414C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972113 | ||||||
chr11:74972119
|
C | T | 2 | a0001c0001t0002g0019a0001c0001t0002g0245 | 4 | NA18942.hp2 NA18949.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+2420C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972119 | ||||||
chr11:74972127
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.494+2428C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972127 | ||||||
chr11:74972158
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.494+2459C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972158 | ||||||
chr11:74972185
|
C | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0289 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+2486C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972185 | ||||||
chr11:74972197
|
C | A | 81 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.494+2498C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972197 | ||||||
chr11:74972200
|
G | C | 81 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.494+2501G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972200 | ||||||
chr11:74972570
|
C | T | 7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0282others(4): Show | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.494+2871C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972570 | ||||||
chr11:74972720
|
CT | C | 8 | a0001c0001t0001g0116a0001c0001t0001g0148a0001c0001t0001g0157others(5): Show | 8 | HG00609.hp2 HG02976.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+3035delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74972720 | |||||
chr11:74972738
|
C | T | 81 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.494+3039C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972738 | ||||||
chr11:74972878
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.494+3179T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972878 | ||||||
chr11:74972878
|
T | TTA | 5 | a0001c0001t0001g0113a0001c0001t0001g0157a0001c0001t0001g0161others(2): Show | 5 | HG01516.hp2 HG01517.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+3195_494+3196d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74972878 | |||||
chr11:74972878
|
TTA | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0067a0001c0001t0001g0069others(7): Show | 12 | HG00639.hp2 HG01074.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.494+3195_494+3196d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74972878 | |||||
chr11:74972893
|
TA | T | 76 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0046others(73): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.494+3195delA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972893 | ||||||
chr11:74972894
|
A | T | 4 | a0001c0001t0001g0123a0001c0001t0001g0145a0001c0001t0002g0260others(1): Show | 4 | HG02109.hp2 HG03041.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+3195A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972894 | ||||||
chr11:74972894
|
AT | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(103): Show | 129 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.494+3206delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74972894 | |||||
chr11:74972894
|
ATT | A | 8 | a0001c0001t0002g0290a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 10 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.494+3205_494+3206d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74972894 | |||||
chr11:74972896
|
T | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(50): Show | 65 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.494+3197T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972896 | ||||||
chr11:74972897
|
T | A | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.494+3198T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972897 | ||||||
chr11:74972898
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.494+3199T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972898 | ||||||
chr11:74972948
|
C | A | 93 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(90): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+3249C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972948 | ||||||
chr11:74972951
|
A | G | 2 | a0001c0001t0002g0288a0001c0001t0002g0290 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.494+3252A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972951 | ||||||
chr11:74973083
|
A | G | 3 | a0001c0001t0002g0241a0001c0001t0002g0258a0001c0001t0002g0265 | 3 | HG00642.hp1 HG00733.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.494+3384A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973083 | ||||||
chr11:74973246
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.494+3547T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973246 | ||||||
chr11:74973274
|
G | A | 2 | a0001c0001t0006g0282a0001c0001t0006g0283 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.494+3575G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973274 | ||||||
chr11:74973517
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.495-3340A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973517 | ||||||
chr11:74973596
|
A | G | 5 | a0001c0001t0001g0163a0001c0001t0008g0063a0001c0001t0008g0064others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.495-3261A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973596 | ||||||
chr11:74973691
|
T | G | 12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0002t0001g0023others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.495-3166T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973691 | ||||||
chr11:74973846
|
C | T | 1 | a0001c0001t0002g0215 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.495-3011C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973846 | ||||||
chr11:74974024
|
T | C | 73 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(70): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.495-2833T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974024 | ||||||
chr11:74974111
|
C | CT | 181 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0013others(178): Show | 225 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.495-2735dupT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74974111 | |||||
chr11:74974228
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.495-2629A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974228 | ||||||
chr11:74974276
|
T | A | 9 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0155others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.495-2581T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974276 | ||||||
chr11:74974307
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C | T | 3 | a0001c0001t0002g0043a0001c0001t0002g0181a0001c0001t0002g0279 | 4 | HG01099.hp2 HG02809.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-2550C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974307 | ||||||
chr11:74974314
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C | G | 1 | a0001c0001t0002g0226 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.495-2543C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974314 | ||||||
chr11:74974367
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G | A | 7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0282others(4): Show | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.495-2490G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974367 | ||||||
chr11:74974383
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C | T | 4 | a0001c0001t0002g0042a0001c0001t0002g0255a0001c0001t0002g0268others(1): Show | 5 | HG00280.hp1 HG01106.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.495-2474C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974383 | ||||||
chr11:74974516
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C | T | 6 | a0001c0001t0002g0215a0001c0001t0002g0216a0001c0001t0002g0234others(3): Show | 6 | HG00323.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-2341C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974516 | ||||||
chr11:74974563
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C | T | 1 | a0001c0001t0003g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.495-2294C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974563 | ||||||
chr11:74974689
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G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0001g0136 | 3 | HG02818.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.495-2168G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974689 | ||||||
chr11:74974743
|
T | G | 1 | a0001c0001t0001g0211 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.495-2114T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974743 | ||||||
chr11:74974763
|
A | T | 93 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0016others(90): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.495-2094A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974763 | ||||||
chr11:74974835
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G | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0090a0001c0001t0001g0115others(3): Show | 6 | NA18951.hp2 NA18989.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-2022G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974835 | ||||||
chr11:74974965
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C | G | 9 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0155others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.495-1892C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974965 | ||||||
chr11:74974988
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G | A | 1 | a0001c0001t0001g0091 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.495-1869G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974988 | ||||||
chr11:74975070
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G | A | 1 | a0001c0001t0002g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495-1787G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975070 | ||||||
chr11:74975149
|
C | G | 12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0002t0001g0023others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.495-1708C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975149 | ||||||
chr11:74975379
|
C | T | 1 | a0001c0001t0003g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.495-1478C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975379 | ||||||
chr11:74975401
|
C | T | 1 | a0001c0001t0003g0119 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.495-1456C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975401 | ||||||
chr11:74975487
|
T | C | 7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0282others(4): Show | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.495-1370T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975487 | ||||||
chr11:74975878
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0096 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.495-979C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975878 | ||||||
chr11:74976013
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.495-844C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976013 | ||||||
chr11:74976180
|
C | T | 12 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0288others(9): Show | 16 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-677C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976180 | ||||||
chr11:74976211
|
C | A | 12 | a0001c0001t0002g0022a0001c0001t0002g0287a0001c0001t0002g0288others(9): Show | 16 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-646C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976211 | ||||||
chr11:74976220
|
C | T | 2 | a0001c0001t0002g0237a0001c0001t0002g0238 | 2 | HG00323.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.495-637C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976220 | ||||||
chr11:74976296
|
A | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(203): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.495-561A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976296 | ||||||
chr11:74976394
|
G | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.495-463G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976394 | ||||||
chr11:74976434
|
C | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG02896.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.495-423C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976434 |