geneid | 64744 |
---|---|
ensemblid | ENSG00000084070.12 |
hgncid | 25082 |
symbol | SMAP2 |
name | small ArfGAP2 |
refseq_nuc | NM_022733.3 |
refseq_prot | NP_073570.1 |
ensembl_nuc | ENST00000372718.8 |
ensembl_prot | ENSP00000361803.3 |
mane_status | MANE Select |
chr | chr1 |
start | 40373727 |
end | 40423322 |
strand | + |
ver | v1.2 |
region | chr1:40373727-40423322 |
region5000 | chr1:40368727-40428322 |
regionname0 | SMAP2_chr1_40373727_40423322 |
regionname5000 | SMAP2_chr1_40368727_40428322 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 429 | 394 | 88 | 60 | 188 | 16 | 40 | 146 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0002 | 0/0 | 429 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0003 | 0/0 | 429 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1290 | 363 | 79 | 53 | 183 | 12 | 35 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
c0002 | 1/0 | 1290 | 18 | 0 | 4 | 5 | 4 | 4 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
c0003 | 0/0 | 1290 | 10 | 8 | 2 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
c0004 | 0/0 | 1290 | 4 | 4 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
c0005 | 0/0 | 1290 | 3 | 1 | 1 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
c0006 | 0/0 | 1290 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1616 | 377 | 81 | 59 | 180 | 15 | 40 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
t0002 | 0/0 | 1616 | 7 | 0 | 1 | 6 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
t0003 | 0/0 | 1615 | 4 | 4 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
t0004 | 0/0 | 1618 | 4 | 4 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
t0005 | 0/0 | 1616 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
t0006 | 0/0 | 1616 | 3 | 3 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
t0007 | 0/0 | 1616 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
t0008 | 0/0 | 1616 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0002 | 0/1 | 8 | 0 | 3 | 1 | 2 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0003 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0004 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0006 | 0/0 | 5 | 2 | 1 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0008 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0009 | 0/0 | 5 | 3 | 1 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1290 | 363 | 79 | 53 | 183 | 12 | 35 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0002 | 1/0 | 1290 | 18 | 0 | 4 | 5 | 4 | 4 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0003 | 0/0 | 1290 | 10 | 8 | 2 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0005 | 0/0 | 1290 | 3 | 1 | 1 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0002c0004 | 0/0 | 1290 | 4 | 4 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0003c0006 | 0/0 | 1290 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2905 | 344 | 72 | 52 | 173 | 11 | 35 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0001t0002 | 0/0 | 2905 | 7 | 0 | 1 | 6 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0001t0003 | 0/0 | 2904 | 4 | 4 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0001t0005 | 0/0 | 2905 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0001t0006 | 0/0 | 2905 | 3 | 3 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0001t0007 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0001t0008 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0002t0001 | 1/0 | 2905 | 18 | 0 | 4 | 5 | 4 | 4 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0003t0001 | 0/0 | 2905 | 10 | 8 | 2 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0001c0005t0001 | 0/0 | 2905 | 3 | 1 | 1 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0002c0004t0004 | 0/0 | 2907 | 4 | 4 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
a0003c0006t0001 | 0/0 | 2905 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | copy fasta | chr1 | 40368727 | 40428322 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0002 | 0/1 | 7 | 0 | 3 | 0 | 2 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0006 | 0/0 | 5 | 2 | 1 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0009 | 0/0 | 5 | 3 | 1 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0005g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0006g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0001t0008g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0001c0005t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0002c0004t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0002c0004t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0002c0004t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0003c0006t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
a0003c0006t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0303 | EUR | GBR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0293 | EUR | FIN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00323 | hp2 | a0001 | c0001 | t0008 | g0302 | EUR | FIN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0105 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0106 | AMR | PUR | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01433 | hp1 | a0001 | c0005 | t0001 | g0101 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0042 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0042 | EUR | IBS | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0102 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01891 | hp1 | a0002 | c0004 | t0004 | g0025 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0296 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02145 | hp1 | a0001 | c0005 | t0001 | g0100 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CDX | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0103 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0107 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02622 | hp2 | a0002 | c0004 | t0004 | g0246 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0300 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0095 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03017 | hp1 | a0001 | c0005 | t0001 | g0099 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0093 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0277 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0235 | AFR | GWD | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03579 | hp1 | a0002 | c0004 | t0004 | g0247 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0294 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0094 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18940 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18997 | hp1 | a0003 | c0006 | t0001 | g0194 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19063 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19085 | hp1 | a0003 | c0006 | t0001 | g0193 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA19240 | hp2 | a0002 | c0004 | t0004 | g0025 | AFR | YRI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ASW | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ASW | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0278 | EUR | TSI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0279 | SAS | GIH | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | GIH | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0104 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | USA | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | USA | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | USA | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | USA | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0299 | REF | REF | SMAP2_chr1_40368727_40428322 | SMAP2 | chr1 | 40368727 | 40428322 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40416797
|
G | A | 1 | a0002 | 4 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.865G>A | p.Ala289Thr | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/10 | 1259/2905 | 865/1290 | 289/429 | chr1 | 40416797 | ||
chr1:40416951
|
T | C | 1 | a0003 | 2 | NA18997.hp1 NA19085.hp1 |
missense_variant | MODERATE | c.1019T>C | p.Met340Thr | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/10 | 1413/2905 | 1019/1290 | 340/429 | chr1 | 40416951 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40415369
|
C | G | 5 | a0001c0001a0001c0003a0001c0005others(2): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
synonymous_variant | LOW | c.669C>G | p.Ser223Ser | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/10 | 1063/2905 | 669/1290 | 223/429 | chr1 | 40415369 | ||
chr1:40417075
|
G | A | 1 | a0001c0005 | 3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
synonymous_variant | LOW | c.1143G>A | p.Gln381Gln | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/10 | 1537/2905 | 1143/1290 | 381/429 | chr1 | 40417075 | ||
chr1:40417081
|
A | G | 1 | a0001c0003 | 10 | HG01069.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
synonymous_variant | LOW | c.1149A>G | p.Gln383Gln | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/10 | 1543/2905 | 1149/1290 | 383/429 | chr1 | 40417081 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40373862
|
G | A | 1 | a0001c0001t0005 | 3 | HG00438.hp2 NA18940.hp2 NA18984.hp2 |
5_prime_UTR_variant | MODIFIER | c.-259G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/10 | 259 | chr1 | 40373862 | |||||
chr1:40374049
|
C | A | 1 | a0001c0001t0002 | 7 | HG00423.hp2 HG01928.hp1 NA18945.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-72C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/10 | 72 | chr1 | 40374049 | |||||
chr1:40422897
|
A | AGT | 1 | a0002c0004t0004 | 4 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*809_*810dupGT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 10/10 | 811 | INFO_REALIGN_3_PRIME | chr1 | 40422897 | ||||
chr1:40422926
|
C | T | 1 | a0001c0001t0006 | 3 | HG01884.hp2 HG02559.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*825C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 10/10 | 825 | chr1 | 40422926 | |||||
chr1:40422935
|
C | T | 1 | a0001c0001t0008 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*834C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 10/10 | 834 | chr1 | 40422935 | |||||
chr1:40423038
|
AT | A | 1 | a0001c0001t0003 | 4 | HG02630.hp2 HG02970.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*938delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 10/10 | 938 | chr1 | 40423038 | |||||
chr1:40423162
|
G | A | 2 | a0001c0001t0007a0002c0004t0004 | 5 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1061G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 10/10 | 1061 | chr1 | 40423162 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40374227
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01167.hp1 | splice_region_variant&intron_variant | LOW | c.103+4G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374227 | ||||||
chr1:40374392
|
G | T | 1 | a0001c0001t0001g0307 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.103+169G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374392 | ||||||
chr1:40374516
|
T | G | 1 | a0001c0001t0001g0046 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.103+293T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374516 | ||||||
chr1:40374556
|
C | G | 1 | a0001c0001t0001g0306 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.103+333C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374556 | ||||||
chr1:40374577
|
T | TTGCG | 55 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0034others(52): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.103+373_103+376dup others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374577 | |||||
chr1:40374596
|
C | CGTGCGT | 6 | a0001c0001t0001g0038a0001c0001t0001g0252a0001c0001t0001g0253others(3): Show | 7 | HG00642.hp1 HG01123.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.103+376_103+377ins others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374596 | |||||
chr1:40374596
|
CGT | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(54): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.103+401_103+402del others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374596 | |||||
chr1:40374596
|
CGTGT | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 6 | HG02109.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+399_103+402del others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374596 | |||||
chr1:40374598
|
T | TGC | 97 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 121 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.103+376_103+377ins others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374598 | |||||
chr1:40374599
|
G | GCGTGTT | 18 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0257others(15): Show | 21 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.103+376_103+377ins others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374599 | ||||||
chr1:40374600
|
T | C | 32 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(29): Show | 37 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.103+377T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374600 | ||||||
chr1:40374602
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(53): Show | 78 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.103+379T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374602 | ||||||
chr1:40374604
|
T | C | 4 | a0001c0001t0001g0048a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 4 | HG02109.hp1 HG04184.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+381T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374604 | ||||||
chr1:40374620
|
T | TGA | 6 | a0001c0002t0001g0042a0001c0002t0001g0275a0001c0002t0001g0276others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.103+398_103+399ins others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374620 | |||||
chr1:40374622
|
T | A | 53 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(50): Show | 64 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.103+399T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374622 | ||||||
chr1:40374622
|
T | TGA | 1 | a0001c0001t0006g0018 | 3 | HG01884.hp2 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.103+400_103+401ins others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374622 | |||||
chr1:40374622
|
T | TGAGA | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.103+400_103+401ins others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374622 | |||||
chr1:40374622
|
TGTGA | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0096a0001c0001t0001g0280 | 4 | HG02165.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+401_103+404del others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374622 | |||||
chr1:40374624
|
T | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(183): Show | 240 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.103+401T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374624 | ||||||
chr1:40374624
|
T | TGA | 6 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0303others(3): Show | 11 | HG00099.hp2 HG00323.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.103+418_103+419dup others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374624 | |||||
chr1:40374624
|
T | TGAGA | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156 | 3 | HG01243.hp1 HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.103+416_103+419dup others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374624 | |||||
chr1:40374624
|
TGA | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0288others(4): Show | 15 | HG00544.hp2 HG00735.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.103+418_103+419del others(2): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40374624 | |||||
chr1:40374626
|
A | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0048a0001c0001t0001g0237others(1): Show | 5 | HG01175.hp2 HG02056.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+403A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374626 | ||||||
chr1:40374677
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.103+454G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374677 | ||||||
chr1:40374681
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 255 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.103+458A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374681 | ||||||
chr1:40374801
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103+578C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40374801 | ||||||
chr1:40375184
|
C | A | 19 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0240others(16): Show | 22 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.103+961C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375184 | ||||||
chr1:40375334
|
C | A | 4 | a0001c0001t0001g0031a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 5 | HG01175.hp2 HG02683.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+1111C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375334 | ||||||
chr1:40375377
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.103+1154T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375377 | ||||||
chr1:40375419
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103+1196C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375419 | ||||||
chr1:40375477
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+1254G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375477 | ||||||
chr1:40375567
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.103+1344T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375567 | ||||||
chr1:40375582
|
C | A | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1359C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375582 | ||||||
chr1:40375593
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1370A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375593 | ||||||
chr1:40375826
|
A | AC | 39 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0048others(36): Show | 41 | HG00408.hp1 HG00558.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.103+1614dupC | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40375826 | |||||
chr1:40375826
|
AC | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(100): Show | 133 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.103+1614delC | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40375826 | |||||
chr1:40375826
|
ACC | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.103+1613_103+1614d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40375826 | |||||
chr1:40375837
|
C | A | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1614C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375837 | ||||||
chr1:40375838
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1615A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375838 | ||||||
chr1:40375942
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1719A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375942 | ||||||
chr1:40375943
|
T | A | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+1720T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375943 | ||||||
chr1:40375982
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0207 | 2 | HG00323.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.103+1759G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40375982 | ||||||
chr1:40376010
|
G | A | 1 | a0001c0001t0002g0231 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.103+1787G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376010 | ||||||
chr1:40376019
|
C | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0240others(16): Show | 22 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.103+1796C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376019 | ||||||
chr1:40376099
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.103+1876C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376099 | ||||||
chr1:40376102
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0205 | 3 | HG00408.hp1 NA18967.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.103+1879C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376102 | ||||||
chr1:40376197
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.103+1974C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376197 | ||||||
chr1:40376238
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0131others(1): Show | 7 | HG02622.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+2015A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376238 | ||||||
chr1:40376242
|
T | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(51): Show | 70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.103+2019T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376242 | ||||||
chr1:40376261
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.103+2038G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376261 | ||||||
chr1:40376675
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+2452G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376675 | ||||||
chr1:40376692
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.103+2469A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376692 | ||||||
chr1:40376816
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103+2593G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376816 | ||||||
chr1:40376818
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+2595G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376818 | ||||||
chr1:40376827
|
C | A | 1 | a0001c0001t0001g0301 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.103+2604C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376827 | ||||||
chr1:40376828
|
A | T | 1 | a0001c0001t0001g0301 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.103+2605A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376828 | ||||||
chr1:40376860
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0239 | 2 | NA18975.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.103+2637A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376860 | ||||||
chr1:40376892
|
A | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.103+2669A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376892 | ||||||
chr1:40376928
|
T | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0163a0001c0001t0001g0188 | 9 | HG00741.hp1 HG01074.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.103+2705T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376928 | ||||||
chr1:40376942
|
T | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.103+2719T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376942 | ||||||
chr1:40376944
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.103+2721C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40376944 | ||||||
chr1:40377226
|
C | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.103+3003C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377226 | ||||||
chr1:40377227
|
G | A | 1 | a0001c0001t0001g0017 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+3004G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377227 | ||||||
chr1:40377253
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.103+3030G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377253 | ||||||
chr1:40377261
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0273others(7): Show | 18 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.103+3038G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377261 | ||||||
chr1:40377433
|
T | A | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+3210T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377433 | ||||||
chr1:40377599
|
G | T | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+3376G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377599 | ||||||
chr1:40377660
|
G | A | 1 | a0001c0001t0008g0302 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.103+3437G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40377660 | ||||||
chr1:40378087
|
A | T | 1 | a0001c0001t0001g0153 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.103+3864A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378087 | ||||||
chr1:40378134
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.103+3911T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378134 | ||||||
chr1:40378147
|
C | T | 70 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(67): Show | 88 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.103+3924C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378147 | ||||||
chr1:40378296
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.103+4073C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378296 | ||||||
chr1:40378344
|
T | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.103+4121T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378344 | ||||||
chr1:40378364
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 123 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.103+4141A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378364 | ||||||
chr1:40378407
|
A | C | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+4184A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378407 | ||||||
chr1:40378453
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0143a0001c0001t0001g0158others(3): Show | 8 | NA18941.hp2 NA18970.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+4230A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378453 | ||||||
chr1:40378727
|
C | G | 1 | a0001c0001t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.103+4504C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378727 | ||||||
chr1:40378730
|
T | G | 16 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0043others(13): Show | 31 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+4507T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378730 | ||||||
chr1:40378939
|
C | T | 1 | a0001c0005t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.103+4716C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40378939 | ||||||
chr1:40378962
|
ATTTCT | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(37): Show | 50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.103+4758_103+4762d others(7): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40378962 | |||||
chr1:40378981
|
CT | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(94): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.103+4773delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40378981 | |||||
chr1:40379030
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(51): Show | 70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.103+4807C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379030 | ||||||
chr1:40379098
|
G | C | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+4875G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379098 | ||||||
chr1:40379099
|
C | G | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.103+4876C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379099 | ||||||
chr1:40379449
|
T | C | 4 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101others(1): Show | 5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+5226T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379449 | ||||||
chr1:40379524
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.103+5301C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379524 | ||||||
chr1:40379555
|
C | CT | 55 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(52): Show | 70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.103+5356dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40379555 | |||||
chr1:40379555
|
C | CTT | 6 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0127others(3): Show | 7 | HG00639.hp2 HG01433.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+5355_103+5356d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40379555 | |||||
chr1:40379555
|
CT | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(106): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.103+5356delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40379555 | |||||
chr1:40379555
|
CTT | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 11 | HG00597.hp1 HG01069.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.103+5355_103+5356d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40379555 | |||||
chr1:40379675
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.103+5452C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379675 | ||||||
chr1:40379707
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.103+5484T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379707 | ||||||
chr1:40379713
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.103+5490G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40379713 | ||||||
chr1:40380309
|
T | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(51): Show | 70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.103+6086T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380309 | ||||||
chr1:40380320
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.103+6097C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380320 | ||||||
chr1:40380457
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.103+6234A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380457 | ||||||
chr1:40380529
|
C | CT | 101 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.103+6317dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40380529 | |||||
chr1:40380529
|
C | CTTTTTT | 47 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0037others(44): Show | 66 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.103+6312_103+6317d others(8): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40380529 | |||||
chr1:40380529
|
C | CTTTTTTT | 148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(145): Show | 190 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.103+6311_103+6317d others(9): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40380529 | |||||
chr1:40380560
|
C | T | 5 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG00558.hp1 NA18942.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+6337C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380560 | ||||||
chr1:40380572
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.103+6349C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380572 | ||||||
chr1:40380693
|
C | A | 8 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0136others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+6470C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380693 | ||||||
chr1:40380750
|
G | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(45): Show | 63 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.103+6527G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380750 | ||||||
chr1:40380813
|
G | A | 8 | a0001c0001t0001g0039a0001c0001t0001g0258a0001c0001t0001g0259others(5): Show | 9 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.103+6590G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380813 | ||||||
chr1:40380934
|
T | C | 1 | a0001c0001t0001g0017 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+6711T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380934 | ||||||
chr1:40380985
|
G | A | 27 | a0001c0001t0001g0029a0001c0001t0001g0133a0001c0001t0001g0134others(24): Show | 31 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+6762G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40380985 | ||||||
chr1:40381142
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.103+6919A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381142 | ||||||
chr1:40381162
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.103+6939G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381162 | ||||||
chr1:40381175
|
C | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.103+6952C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381175 | ||||||
chr1:40381383
|
T | C | 2 | a0001c0003t0001g0102a0001c0003t0001g0107 | 2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.103+7160T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381383 | ||||||
chr1:40381559
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.103+7336G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381559 | ||||||
chr1:40381740
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.103+7517A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381740 | ||||||
chr1:40381819
|
A | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 123 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.103+7596A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40381819 | ||||||
chr1:40381940
|
CT | C | 27 | a0001c0001t0001g0029a0001c0001t0001g0133a0001c0001t0001g0134others(24): Show | 31 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+7719delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40381940 | |||||
chr1:40382150
|
T | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0273others(7): Show | 18 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.103+7927T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40382150 | ||||||
chr1:40382197
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.103+7974C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40382197 | ||||||
chr1:40382762
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.103+8539T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40382762 | ||||||
chr1:40382769
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103+8546T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40382769 | ||||||
chr1:40382914
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.103+8691G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40382914 | ||||||
chr1:40383149
|
G | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.103+8926G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383149 | ||||||
chr1:40383158
|
T | A | 70 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(67): Show | 88 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.103+8935T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383158 | ||||||
chr1:40383276
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.103+9053G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383276 | ||||||
chr1:40383319
|
G | GCTC | 4 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101others(1): Show | 5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+9099_103+9101d others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40383319 | |||||
chr1:40383531
|
G | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0273others(7): Show | 18 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.103+9308G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383531 | ||||||
chr1:40383703
|
G | A | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.103+9480G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383703 | ||||||
chr1:40383759
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.103+9536A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40383759 | ||||||
chr1:40384007
|
A | G | 1 | a0001c0001t0001g0017 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+9784A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384007 | ||||||
chr1:40384105
|
C | T | 1 | a0001c0005t0001g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.103+9882C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384105 | ||||||
chr1:40384339
|
A | T | 26 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(23): Show | 31 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+10116A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384339 | ||||||
chr1:40384484
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0075 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.103+10261T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384484 | ||||||
chr1:40384534
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02615.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.103+10311A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384534 | ||||||
chr1:40384559
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0092 | 2 | NA18977.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.103+10336T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384559 | ||||||
chr1:40384615
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.103+10392G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384615 | ||||||
chr1:40384914
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0157 | 4 | HG02723.hp1 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+10691T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384914 | ||||||
chr1:40384941
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.103+10718G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40384941 | ||||||
chr1:40385041
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+10818C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40385041 | ||||||
chr1:40385079
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0157 | 4 | HG02723.hp1 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+10856C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40385079 | ||||||
chr1:40385421
|
T | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0184 | 3 | HG01496.hp2 HG02074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.103+11198T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40385421 | ||||||
chr1:40385455
|
G | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+11232G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40385455 | ||||||
chr1:40385697
|
C | T | 4 | a0001c0001t0001g0191a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG00733.hp1 HG01099.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+11474C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40385697 | ||||||
chr1:40385874
|
A | AT | 27 | a0001c0001t0001g0029a0001c0001t0001g0133a0001c0001t0001g0134others(24): Show | 31 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+11652dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40385874 | |||||
chr1:40386030
|
G | A | 27 | a0001c0001t0001g0029a0001c0001t0001g0133a0001c0001t0001g0134others(24): Show | 31 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+11807G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386030 | ||||||
chr1:40386042
|
G | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+11819G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386042 | ||||||
chr1:40386190
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.103+11967C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386190 | ||||||
chr1:40386269
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0269 | 2 | HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.103+12046A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386269 | ||||||
chr1:40386435
|
A | G | 1 | a0001c0001t0001g0034 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.103+12212A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386435 | ||||||
chr1:40386462
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.103+12239T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386462 | ||||||
chr1:40386660
|
GTTT | G | 26 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(23): Show | 31 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+12439_103+1244 others(7): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40386660 | |||||
chr1:40386665
|
C | G | 26 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(23): Show | 31 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+12442C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386665 | ||||||
chr1:40386668
|
T | A | 26 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(23): Show | 31 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+12445T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386668 | ||||||
chr1:40386669
|
C | T | 26 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(23): Show | 31 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+12446C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386669 | ||||||
chr1:40386676
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103+12453G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386676 | ||||||
chr1:40386691
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.103+12468G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386691 | ||||||
chr1:40386710
|
T | G | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(37): Show | 50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.103+12487T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386710 | ||||||
chr1:40386716
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.103+12493T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386716 | ||||||
chr1:40386740
|
G | GT | 4 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0131others(1): Show | 7 | HG02622.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+12525dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40386740 | |||||
chr1:40386750
|
AAAC | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 255 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.103+12537_103+1253 others(7): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40386750 | |||||
chr1:40386841
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0211a0001c0001t0001g0212 | 4 | HG03491.hp2 HG03492.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+12618T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386841 | ||||||
chr1:40386853
|
C | CT | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(111): Show | 151 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.103+12648dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40386853 | |||||
chr1:40386853
|
C | CTT | 7 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0091others(4): Show | 12 | HG00099.hp2 HG01106.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.103+12647_103+1264 others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40386853 | |||||
chr1:40386886
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0252 | 3 | HG01123.hp1 HG01256.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.103+12663T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386886 | ||||||
chr1:40386892
|
C | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0240others(16): Show | 22 | HG02055.hp1 HG02280.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.103+12669C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386892 | ||||||
chr1:40386977
|
A | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | NA18943.hp2 NA18947.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.103+12754A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40386977 | ||||||
chr1:40387131
|
G | A | 1 | a0001c0001t0001g0017 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+12908G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387131 | ||||||
chr1:40387143
|
A | T | 4 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101others(1): Show | 5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+12920A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387143 | ||||||
chr1:40387149
|
G | A | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.103+12926G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387149 | ||||||
chr1:40387172
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.103+12949T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387172 | ||||||
chr1:40387240
|
A | C | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.103+13017A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387240 | ||||||
chr1:40387264
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.103+13041G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387264 | ||||||
chr1:40387399
|
T | G | 2 | a0001c0005t0001g0099a0001c0005t0001g0101 | 2 | HG01433.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.103+13176T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387399 | ||||||
chr1:40387411
|
G | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | NA18967.hp2 NA18968.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.103+13188G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387411 | ||||||
chr1:40387418
|
G | C | 1 | a0001c0001t0001g0170 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.103+13195G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387418 | ||||||
chr1:40387522
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.103+13299A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387522 | ||||||
chr1:40387611
|
A | AG | 80 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(77): Show | 98 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.103+13391dupG | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40387611 | |||||
chr1:40387659
|
G | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(77): Show | 98 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.103+13436G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387659 | ||||||
chr1:40387696
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0130 | 2 | NA18951.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.103+13473C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387696 | ||||||
chr1:40387709
|
C | T | 1 | a0001c0001t0001g0031 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.103+13486C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387709 | ||||||
chr1:40387713
|
C | T | 1 | a0001c0003t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103+13490C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387713 | ||||||
chr1:40387753
|
G | A | 1 | a0001c0001t0001g0017 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+13530G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387753 | ||||||
chr1:40387817
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.103+13594C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387817 | ||||||
chr1:40387910
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.103+13687C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387910 | ||||||
chr1:40387920
|
T | TG | 16 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0043others(13): Show | 31 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+13700dupG | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40387920 | |||||
chr1:40387951
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.103+13728C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40387951 | ||||||
chr1:40388037
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.103+13814C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388037 | ||||||
chr1:40388054
|
G | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.103+13831G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388054 | ||||||
chr1:40388068
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.103+13845C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388068 | ||||||
chr1:40388089
|
C | T | 2 | a0001c0001t0001g0139a0001c0003t0001g0235 | 2 | HG03540.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.103+13866C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388089 | ||||||
chr1:40388137
|
A | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.103+13914A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388137 | ||||||
chr1:40388220
|
A | G | 4 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101others(1): Show | 5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+13997A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388220 | ||||||
chr1:40388288
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103+14065T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388288 | ||||||
chr1:40388371
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.103+14148C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388371 | ||||||
chr1:40388458
|
CGACACTC others(43): Show |
C | 1 | a0001c0001t0001g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.103+14259_103+1430 others(54): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40388458 | |||||
chr1:40388562
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103+14339C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388562 | ||||||
chr1:40388612
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.103+14389G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388612 | ||||||
chr1:40388663
|
C | G | 1 | a0001c0001t0001g0198 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.103+14440C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40388663 | ||||||
chr1:40389059
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.103+14836G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389059 | ||||||
chr1:40389070
|
C | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.103+14847C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389070 | ||||||
chr1:40389096
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103+14873A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389096 | ||||||
chr1:40389180
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.103+14957A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389180 | ||||||
chr1:40389309
|
AT | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 399 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.103+15096delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40389309 | |||||
chr1:40389473
|
G | GT | 81 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(78): Show | 99 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.103+15256dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40389473 | |||||
chr1:40389506
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.103+15283A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389506 | ||||||
chr1:40389730
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.103+15507T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389730 | ||||||
chr1:40389756
|
G | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0096 | 3 | HG02258.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103+15533G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389756 | ||||||
chr1:40389918
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(78): Show | 99 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.103+15695C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389918 | ||||||
chr1:40389924
|
C | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 5 | NA18943.hp2 NA18947.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+15701C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389924 | ||||||
chr1:40389932
|
C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(52): Show | 71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.103+15709C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389932 | ||||||
chr1:40389983
|
G | C | 1 | a0001c0001t0001g0307 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.103+15760G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40389983 | ||||||
chr1:40390019
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 389 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(386): Show |
intron_variant | MODIFIER | c.103+15796A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40390019 | ||||||
chr1:40390419
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.103+16196T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40390419 | ||||||
chr1:40390974
|
GA | G | 27 | a0001c0001t0001g0029a0001c0001t0001g0133a0001c0001t0001g0134others(24): Show | 31 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.104-15761delA | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40390974 | ||||||
chr1:40391023
|
G | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.104-15713G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391023 | ||||||
chr1:40391038
|
T | C | 2 | a0002c0004t0004g0246a0002c0004t0004g0247 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.104-15698T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391038 | ||||||
chr1:40391104
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(78): Show | 99 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.104-15632C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391104 | ||||||
chr1:40391235
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.104-15501A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391235 | ||||||
chr1:40391252
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 389 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(386): Show |
intron_variant | MODIFIER | c.104-15484A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391252 | ||||||
chr1:40391293
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.104-15443A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391293 | ||||||
chr1:40391308
|
T | C | 2 | a0002c0004t0004g0246a0002c0004t0004g0247 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.104-15428T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391308 | ||||||
chr1:40391691
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104-15045T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391691 | ||||||
chr1:40391858
|
A | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.104-14878A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391858 | ||||||
chr1:40391998
|
A | G | 8 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0136others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-14738A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40391998 | ||||||
chr1:40392026
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.104-14710T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392026 | ||||||
chr1:40392080
|
A | G | 4 | a0001c0001t0001g0068a0001c0001t0001g0098a0001c0001t0001g0197others(1): Show | 4 | NA18747.hp1 NA18995.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-14656A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392080 | ||||||
chr1:40392390
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.104-14346C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392390 | ||||||
chr1:40392447
|
C | A | 2 | a0001c0002t0001g0275a0001c0002t0001g0276 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.104-14289C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392447 | ||||||
chr1:40392609
|
AGCAGGGT others(202): Show |
A | 1 | a0001c0001t0001g0227 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.104-14124_104-1391 others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40392609 | |||||
chr1:40392772
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0059 | 2 | HG02155.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.104-13964A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392772 | ||||||
chr1:40392836
|
A | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0181others(1): Show | 4 | NA18941.hp1 NA18956.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-13900A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392836 | ||||||
chr1:40392873
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0232 | 3 | NA18747.hp2 NA18957.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.104-13863G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392873 | ||||||
chr1:40392884
|
G | C | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.104-13852G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392884 | ||||||
chr1:40392898
|
G | C | 83 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(80): Show | 101 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.104-13838G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40392898 | ||||||
chr1:40393011
|
G | A | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.104-13725G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393011 | ||||||
chr1:40393101
|
C | CA | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 320 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.104-13622dupA | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393101 | |||||
chr1:40393101
|
C | CAA | 42 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017others(39): Show | 54 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.104-13623_104-1362 others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393101 | |||||
chr1:40393204
|
T | TAGTC | 83 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(80): Show | 101 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.104-13531_104-1352 others(8): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393204 | |||||
chr1:40393315
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104-13421A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393315 | ||||||
chr1:40393380
|
C | T | 2 | a0002c0004t0004g0246a0002c0004t0004g0247 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.104-13356C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393380 | ||||||
chr1:40393407
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.104-13329A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393407 | ||||||
chr1:40393541
|
C | CT | 7 | a0001c0001t0001g0017a0001c0001t0001g0286a0001c0002t0001g0019others(4): Show | 11 | HG01943.hp2 HG02145.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.104-13173dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393541 | |||||
chr1:40393541
|
CT | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(156): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.104-13173delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393541 | |||||
chr1:40393541
|
CTT | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(101): Show | 136 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.104-13174_104-1317 others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40393541 | |||||
chr1:40393563
|
T | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(37): Show | 50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.104-13173T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393563 | ||||||
chr1:40393864
|
A | C | 4 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101others(1): Show | 5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-12872A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393864 | ||||||
chr1:40393865
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0156 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.104-12871G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40393865 | ||||||
chr1:40394052
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104-12684C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394052 | ||||||
chr1:40394110
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG00408.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.104-12626G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394110 | ||||||
chr1:40394516
|
C | G | 1 | a0001c0001t0001g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.104-12220C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394516 | ||||||
chr1:40394685
|
C | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.104-12051C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394685 | ||||||
chr1:40394747
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104-11989G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394747 | ||||||
chr1:40394758
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.104-11978C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394758 | ||||||
chr1:40394794
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.104-11942G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394794 | ||||||
chr1:40394975
|
C | T | 1 | a0001c0005t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.104-11761C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40394975 | ||||||
chr1:40395044
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.104-11692G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395044 | ||||||
chr1:40395049
|
A | G | 1 | a0001c0001t0001g0017 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.104-11687A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395049 | ||||||
chr1:40395082
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.104-11654T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395082 | ||||||
chr1:40395317
|
G | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0184 | 3 | HG01496.hp2 HG02074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.104-11419G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395317 | ||||||
chr1:40395437
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0157 | 4 | HG02723.hp1 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-11299T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395437 | ||||||
chr1:40395468
|
G | A | 1 | a0001c0001t0001g0010 | 3 | NA18939.hp2 NA18980.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.104-11268G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395468 | ||||||
chr1:40395520
|
A | AAAT | 48 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017others(45): Show | 62 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.104-11195_104-1119 others(7): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40395520 | |||||
chr1:40395577
|
T | TACTAAAA others(14): Show |
293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.104-11157_104-1115 others(25): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40395577 | |||||
chr1:40395733
|
G | T | 1 | a0002c0004t0004g0025 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.104-11003G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395733 | ||||||
chr1:40395760
|
A | C | 1 | a0001c0001t0001g0273 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.104-10976A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395760 | ||||||
chr1:40395970
|
G | C | 1 | a0001c0001t0001g0303 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.104-10766G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40395970 | ||||||
chr1:40396077
|
G | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0036others(42): Show | 65 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.104-10659G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396077 | ||||||
chr1:40396117
|
T | TCTTTCCG others(5): Show |
1 | a0001c0001t0001g0220 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10617_104-1061 others(16): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40396117 | |||||
chr1:40396121
|
C | G | 1 | a0001c0001t0001g0220 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10615C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396121 | ||||||
chr1:40396127
|
T | G | 1 | a0001c0001t0001g0220 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10609T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396127 | ||||||
chr1:40396128
|
C | A | 1 | a0001c0001t0001g0220 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10608C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396128 | ||||||
chr1:40396139
|
C | A | 1 | a0001c0001t0001g0220 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10597C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396139 | ||||||
chr1:40396142
|
C | G | 1 | a0001c0001t0001g0220 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.104-10594C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396142 | ||||||
chr1:40396168
|
A | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-10568A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396168 | ||||||
chr1:40396192
|
G | A | 1 | a0001c0001t0006g0018 | 3 | HG01884.hp2 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.104-10544G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396192 | ||||||
chr1:40396229
|
A | G | 17 | a0001c0001t0001g0029a0001c0001t0001g0144a0001c0001t0001g0145others(14): Show | 21 | HG00423.hp2 HG00438.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.104-10507A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396229 | ||||||
chr1:40396467
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.104-10269T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396467 | ||||||
chr1:40396589
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104-10147A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396589 | ||||||
chr1:40396825
|
G | A | 5 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0181others(2): Show | 5 | HG02056.hp2 NA18941.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-9911G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396825 | ||||||
chr1:40396897
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.104-9839G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396897 | ||||||
chr1:40396986
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0157 | 4 | HG02723.hp1 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-9750C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40396986 | ||||||
chr1:40397057
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104-9679C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397057 | ||||||
chr1:40397104
|
G | A | 1 | a0001c0002t0001g0293 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.104-9632G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397104 | ||||||
chr1:40397159
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(85): Show | 121 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.104-9577G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397159 | ||||||
chr1:40397229
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104-9507A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397229 | ||||||
chr1:40397680
|
CATTGCCT others(4): Show |
C | 1 | a0002c0004t0004g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.104-9055_104-9045d others(13): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397680 | ||||||
chr1:40397692
|
G | T | 1 | a0002c0004t0004g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.104-9044G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397692 | ||||||
chr1:40397725
|
G | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-9011G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397725 | ||||||
chr1:40397913
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104-8823G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40397913 | ||||||
chr1:40398094
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104-8642A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398094 | ||||||
chr1:40398095
|
T | A | 1 | a0001c0005t0001g0099 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.104-8641T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398095 | ||||||
chr1:40398332
|
C | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-8404C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398332 | ||||||
chr1:40398342
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.104-8394G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398342 | ||||||
chr1:40398342
|
G | GC | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.104-8393dupC | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40398342 | |||||
chr1:40398412
|
A | AC | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 122 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.104-8324_104-8323i others(3): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398412 | ||||||
chr1:40398420
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.104-8316G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398420 | ||||||
chr1:40398517
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104-8219G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398517 | ||||||
chr1:40398596
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.104-8140T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398596 | ||||||
chr1:40398624
|
G | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-8112G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398624 | ||||||
chr1:40398837
|
G | T | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.104-7899G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398837 | ||||||
chr1:40398862
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.104-7874A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398862 | ||||||
chr1:40398872
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.104-7864G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398872 | ||||||
chr1:40398986
|
T | C | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.104-7750T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40398986 | ||||||
chr1:40399184
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.104-7552G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399184 | ||||||
chr1:40399205
|
T | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.104-7531T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399205 | ||||||
chr1:40399310
|
A | AT | 7 | a0001c0002t0001g0042a0001c0002t0001g0276a0001c0002t0001g0278others(4): Show | 8 | HG00735.hp1 HG01169.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-7405dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | |||||
chr1:40399310
|
A | ATT | 5 | a0001c0001t0001g0017a0001c0005t0001g0099a0001c0005t0001g0100others(2): Show | 8 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-7406_104-7405d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | |||||
chr1:40399310
|
A | ATTT | 22 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0027others(19): Show | 37 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.104-7407_104-7405d others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | |||||
chr1:40399310
|
A | ATTTT | 127 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 158 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.104-7408_104-7405d others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | |||||
chr1:40399310
|
A | ATTTTT | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 96 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.104-7409_104-7405d others(7): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | |||||
chr1:40399310
|
A | ATTTTTT | 22 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0051others(19): Show | 25 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.104-7410_104-7405d others(8): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399310 | |||||
chr1:40399319
|
T | TTTA | 5 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0072others(2): Show | 8 | HG02080.hp2 HG02155.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-7415_104-7414i others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399319 | |||||
chr1:40399320
|
T | TTA | 30 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 44 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.104-7415_104-7414i others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399320 | |||||
chr1:40399325
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104-7411T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399325 | ||||||
chr1:40399326
|
T | A | 1 | a0001c0001t0001g0081 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.104-7410T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399326 | ||||||
chr1:40399332
|
G | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-7404G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399332 | ||||||
chr1:40399400
|
T | C | 1 | a0001c0002t0001g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.104-7336T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399400 | ||||||
chr1:40399450
|
G | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0087a0001c0001t0001g0089 | 3 | HG01891.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.104-7286G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399450 | ||||||
chr1:40399498
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.104-7238T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399498 | ||||||
chr1:40399629
|
C | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 52 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.104-7107C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399629 | ||||||
chr1:40399656
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104-7080C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399656 | ||||||
chr1:40399701
|
CA | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(168): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.104-7022delA | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399701 | |||||
chr1:40399709
|
AAAAAAG | A | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(79): Show | 100 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.104-7022_104-7017d others(8): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399709 | |||||
chr1:40399772
|
T | TA | 37 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(34): Show | 54 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.104-6955dupA | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40399772 | |||||
chr1:40399796
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.104-6940G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399796 | ||||||
chr1:40399940
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0126 | 2 | NA18940.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.104-6796G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399940 | ||||||
chr1:40399961
|
G | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0036others(42): Show | 65 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.104-6775G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40399961 | ||||||
chr1:40400034
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.104-6702G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400034 | ||||||
chr1:40400036
|
G | A | 1 | a0001c0001t0001g0017 | 3 | HG02723.hp1 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.104-6700G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400036 | ||||||
chr1:40400129
|
G | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0043others(13): Show | 31 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.104-6607G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400129 | ||||||
chr1:40400296
|
A | G | 1 | a0001c0002t0001g0298 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.104-6440A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400296 | ||||||
chr1:40400379
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104-6357A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400379 | ||||||
chr1:40400616
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0029others(76): Show | 104 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.104-6120C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400616 | ||||||
chr1:40400649
|
TGAA | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0280others(5): Show | 16 | HG00544.hp2 HG00735.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.104-6083_104-6081d others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40400649 | |||||
chr1:40400818
|
CTGG | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 378 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(375): Show |
intron_variant | MODIFIER | c.104-5911_104-5909d others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40400818 | |||||
chr1:40400862
|
C | T | 6 | a0001c0002t0001g0042a0001c0002t0001g0275a0001c0002t0001g0276others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-5874C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40400862 | ||||||
chr1:40401127
|
A | G | 23 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(20): Show | 36 | HG00408.hp1 HG00639.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.104-5609A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401127 | ||||||
chr1:40401129
|
C | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(20): Show | 36 | HG00408.hp1 HG00639.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.104-5607C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401129 | ||||||
chr1:40401130
|
G | A | 1 | a0001c0003t0001g0104 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.104-5606G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401130 | ||||||
chr1:40401146
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 264 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.104-5590T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401146 | ||||||
chr1:40401179
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 262 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.104-5557C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401179 | ||||||
chr1:40401186
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(329): Show |
intron_variant | MODIFIER | c.104-5550T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401186 | ||||||
chr1:40401254
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0252 | 3 | HG01123.hp1 HG01256.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.104-5482T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401254 | ||||||
chr1:40401273
|
A | G | 4 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101others(1): Show | 5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-5463A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401273 | ||||||
chr1:40401365
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.104-5371A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401365 | ||||||
chr1:40401490
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.104-5246C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40401490 | ||||||
chr1:40402129
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(50): Show | 69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.104-4607A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402129 | ||||||
chr1:40402301
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.104-4435G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402301 | ||||||
chr1:40402460
|
T | G | 1 | a0001c0001t0001g0056 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.104-4276T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402460 | ||||||
chr1:40402461
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.104-4275T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402461 | ||||||
chr1:40402613
|
C | T | 1 | a0001c0002t0001g0042 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.104-4123C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402613 | ||||||
chr1:40402669
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104-4067A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402669 | ||||||
chr1:40402744
|
G | A | 4 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101others(1): Show | 5 | HG01433.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-3992G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402744 | ||||||
chr1:40402870
|
C | G | 1 | a0001c0001t0001g0121 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.104-3866C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40402870 | ||||||
chr1:40403229
|
A | C | 1 | a0001c0001t0001g0217 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.104-3507A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403229 | ||||||
chr1:40403276
|
C | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0043others(13): Show | 31 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.104-3460C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403276 | ||||||
chr1:40403282
|
C | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.104-3454C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403282 | ||||||
chr1:40403373
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.104-3363C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403373 | ||||||
chr1:40403412
|
C | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.104-3324C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403412 | ||||||
chr1:40403454
|
A | C | 2 | a0002c0004t0004g0246a0002c0004t0004g0247 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.104-3282A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403454 | ||||||
chr1:40403461
|
C | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0113a0001c0001t0001g0124 | 3 | HG02602.hp2 NA18985.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.104-3275C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403461 | ||||||
chr1:40403600
|
A | G | 19 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0043others(16): Show | 34 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.104-3136A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403600 | ||||||
chr1:40403713
|
G | A | 3 | a0001c0003t0001g0102a0001c0003t0001g0104a0001c0003t0001g0107 | 3 | HG01884.hp1 HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.104-3023G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403713 | ||||||
chr1:40403884
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.104-2852A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403884 | ||||||
chr1:40403916
|
T | C | 8 | a0001c0001t0001g0039a0001c0001t0001g0258a0001c0001t0001g0259others(5): Show | 9 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-2820T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40403916 | ||||||
chr1:40404046
|
C | CTTGCCTT others(9): Show |
1 | a0001c0001t0001g0119 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.104-2690_104-2689i others(18): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404046 | ||||||
chr1:40404047
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.104-2689A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404047 | ||||||
chr1:40404088
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0257others(2): Show | 8 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-2648A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404088 | ||||||
chr1:40404473
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0082a0001c0001t0001g0091 | 3 | NA18984.hp1 NA19002.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.104-2263T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404473 | ||||||
chr1:40404791
|
CAT | C | 3 | a0002c0004t0004g0025a0002c0004t0004g0246a0002c0004t0004g0247 | 4 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-1944_104-1943d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404791 | ||||||
chr1:40404873
|
C | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(39): Show | 52 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.104-1863C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40404873 | ||||||
chr1:40405102
|
TAC | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(79): Show | 100 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.104-1632_104-1631d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 40405102 | |||||
chr1:40405573
|
C | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(37): Show | 50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.104-1163C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40405573 | ||||||
chr1:40405631
|
A | G | 27 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0133others(24): Show | 32 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.104-1105A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40405631 | ||||||
chr1:40405745
|
A | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.104-991A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40405745 | ||||||
chr1:40405825
|
A | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.104-911A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40405825 | ||||||
chr1:40406449
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.104-287G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40406449 | ||||||
chr1:40406523
|
G | A | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.104-213G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40406523 | ||||||
chr1:40406684
|
G | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0036others(38): Show | 60 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.104-52G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 1/9 | chr1 | 40406684 | ||||||
chr1:40406937
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0250 | 2 | NA18955.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.237+68A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40406937 | ||||||
chr1:40406951
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(111): Show | 158 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.237+82C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40406951 | ||||||
chr1:40406968
|
G | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0181a0001c0001t0001g0203 | 3 | NA18956.hp1 NA19000.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.237+99G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40406968 | ||||||
chr1:40407034
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.237+165A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407034 | ||||||
chr1:40407067
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.237+198C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407067 | ||||||
chr1:40407092
|
C | T | 3 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101 | 3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.237+223C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407092 | ||||||
chr1:40407319
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.237+450C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407319 | ||||||
chr1:40407521
|
A | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0266a0001c0001t0001g0269 | 3 | HG03195.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.237+652A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407521 | ||||||
chr1:40407538
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.237+669A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407538 | ||||||
chr1:40407749
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.237+880G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407749 | ||||||
chr1:40407788
|
TATC | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02615.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-861_238-859del others(3): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 40407788 | |||||
chr1:40407993
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0257others(2): Show | 8 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-660G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40407993 | ||||||
chr1:40408126
|
A | G | 1 | a0001c0001t0006g0018 | 3 | HG01884.hp2 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.238-527A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40408126 | ||||||
chr1:40408337
|
T | A | 1 | a0001c0001t0001g0215 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.238-316T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 2/9 | chr1 | 40408337 | ||||||
chr1:40408916
|
G | A | 1 | a0001c0002t0001g0296 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.323+178G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40408916 | ||||||
chr1:40409017
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.323+279A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409017 | ||||||
chr1:40409076
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.323+338C>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409076 | ||||||
chr1:40409272
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0143a0001c0001t0001g0158others(3): Show | 8 | NA18941.hp2 NA18970.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.324-485T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409272 | ||||||
chr1:40409312
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.324-445T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409312 | ||||||
chr1:40409382
|
A | T | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.324-375A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409382 | ||||||
chr1:40409550
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.324-207A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 3/9 | chr1 | 40409550 | ||||||
chr1:40410072
|
A | G | 3 | a0001c0001t0001g0139a0001c0001t0001g0175a0001c0001t0001g0196 | 3 | HG00558.hp2 NA18612.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.402+237A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410072 | ||||||
chr1:40410109
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0239 | 2 | NA18975.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.402+274G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410109 | ||||||
chr1:40410152
|
C | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.402+317C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410152 | ||||||
chr1:40410162
|
C | T | 3 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101 | 3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.402+327C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410162 | ||||||
chr1:40410441
|
A | G | 76 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0022others(73): Show | 101 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.402+606A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410441 | ||||||
chr1:40410612
|
C | G | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(37): Show | 50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.402+777C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410612 | ||||||
chr1:40410682
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.402+847A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410682 | ||||||
chr1:40410783
|
C | G | 33 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 49 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.402+948C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410783 | ||||||
chr1:40410829
|
T | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.402+994T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40410829 | ||||||
chr1:40411329
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.402+1494G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411329 | ||||||
chr1:40411368
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(19): Show | 38 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.402+1533C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411368 | ||||||
chr1:40411439
|
GC | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0073 | 4 | NA18960.hp1 NA18974.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-1576delC | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411439 | ||||||
chr1:40411442
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.403-1574A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411442 | ||||||
chr1:40411446
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.403-1570G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411446 | ||||||
chr1:40411514
|
T | G | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.403-1502T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411514 | ||||||
chr1:40411540
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.403-1476G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411540 | ||||||
chr1:40411599
|
G | A | 72 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(69): Show | 90 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.403-1417G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411599 | ||||||
chr1:40411764
|
TGTC | T | 4 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | HG03704.hp2 HG03831.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-1249_403-1247d others(5): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 40411764 | |||||
chr1:40411794
|
G | A | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.403-1222G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411794 | ||||||
chr1:40411809
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.403-1207G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411809 | ||||||
chr1:40411911
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0098a0001c0001t0001g0197 | 3 | NA18995.hp1 NA19058.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.403-1105C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411911 | ||||||
chr1:40411972
|
G | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(31): Show | 50 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.403-1044G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40411972 | ||||||
chr1:40412192
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.403-824G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40412192 | ||||||
chr1:40412224
|
G | A | 6 | a0001c0002t0001g0042a0001c0002t0001g0275a0001c0002t0001g0276others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.403-792G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40412224 | ||||||
chr1:40412820
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.403-196C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40412820 | ||||||
chr1:40412836
|
C | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.403-180C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 4/9 | chr1 | 40412836 | ||||||
chr1:40413137
|
C | T | 27 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0133others(24): Show | 32 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.489+35C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413137 | ||||||
chr1:40413239
|
C | G | 1 | a0001c0003t0001g0235 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.489+137C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413239 | ||||||
chr1:40413265
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.489+163G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413265 | ||||||
chr1:40413265
|
GT | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+165delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 40413265 | |||||
chr1:40413278
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.489+176G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413278 | ||||||
chr1:40413303
|
C | T | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0135others(4): Show | 9 | HG00639.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+201C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413303 | ||||||
chr1:40413325
|
T | G | 1 | a0001c0001t0001g0199 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.489+223T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413325 | ||||||
chr1:40413582
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.489+480G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413582 | ||||||
chr1:40413843
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-316C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413843 | ||||||
chr1:40413890
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.490-269G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413890 | ||||||
chr1:40413962
|
C | G | 1 | a0001c0001t0001g0013 | 3 | NA18941.hp2 NA18970.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.490-197C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413962 | ||||||
chr1:40413964
|
T | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.490-195T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40413964 | ||||||
chr1:40414108
|
A | G | 4 | a0001c0001t0001g0191a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG00733.hp1 HG01099.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-51A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40414108 | ||||||
chr1:40414136
|
G | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(37): Show | 50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.490-23G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40414136 | ||||||
chr1:40414136
|
G | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.490-23G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 5/9 | chr1 | 40414136 | ||||||
chr1:40414280
|
T | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(111): Show | 158 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.571+40T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414280 | ||||||
chr1:40414404
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.571+164G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414404 | ||||||
chr1:40414434
|
G | A | 3 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101 | 3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.571+194G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414434 | ||||||
chr1:40414528
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.571+288C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414528 | ||||||
chr1:40414840
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.572-432T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414840 | ||||||
chr1:40414887
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.572-385G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414887 | ||||||
chr1:40414985
|
A | G | 22 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(19): Show | 26 | HG00639.hp2 HG02055.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.572-287A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414985 | ||||||
chr1:40414990
|
C | T | 2 | a0001c0003t0001g0105a0001c0003t0001g0106 | 2 | HG01069.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.572-282C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40414990 | ||||||
chr1:40415013
|
C | T | 72 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(69): Show | 90 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.572-259C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40415013 | ||||||
chr1:40415076
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.572-196T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40415076 | ||||||
chr1:40415132
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(39): Show | 57 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.572-140C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 6/9 | chr1 | 40415132 | ||||||
chr1:40415517
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.681+136A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415517 | ||||||
chr1:40415575
|
A | G | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(79): Show | 100 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.681+194A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415575 | ||||||
chr1:40415657
|
T | G | 1 | a0001c0001t0001g0249 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.681+276T>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415657 | ||||||
chr1:40415661
|
T | A | 1 | a0001c0001t0001g0274 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.681+280T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415661 | ||||||
chr1:40415674
|
A | G | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0135others(4): Show | 9 | HG00639.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.681+293A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415674 | ||||||
chr1:40415723
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058 | 3 | NA18957.hp2 NA18991.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.681+342C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415723 | ||||||
chr1:40415775
|
A | C | 1 | a0001c0001t0001g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.681+394A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415775 | ||||||
chr1:40415955
|
G | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 49 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.682-221G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40415955 | ||||||
chr1:40416168
|
G | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 49 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(46): Show |
splice_region_variant&intron_variant | LOW | c.682-8G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 7/9 | chr1 | 40416168 | ||||||
chr1:40416360
|
A | G | 3 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101 | 3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.847+19A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 8/9 | chr1 | 40416360 | ||||||
chr1:40417228
|
C | CT | 65 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(62): Show | 86 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1164+151dupT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 40417228 | |||||
chr1:40417423
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(35): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1164+327C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417423 | ||||||
chr1:40417460
|
A | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0036others(38): Show | 60 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1164+364A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417460 | ||||||
chr1:40417509
|
AAG | A | 3 | a0002c0004t0004g0025a0002c0004t0004g0246a0002c0004t0004g0247 | 4 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+417_1164+418d others(4): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 40417509 | |||||
chr1:40417559
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0225 | 2 | NA18947.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1164+463C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417559 | ||||||
chr1:40417572
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1164+476A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417572 | ||||||
chr1:40417593
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1164+497C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417593 | ||||||
chr1:40417594
|
A | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(379): Show |
intron_variant | MODIFIER | c.1164+498A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417594 | ||||||
chr1:40417692
|
C | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02615.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1164+596C>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417692 | ||||||
chr1:40417712
|
C | T | 3 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101 | 3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1164+616C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417712 | ||||||
chr1:40417851
|
C | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(37): Show | 50 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1164+755C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40417851 | ||||||
chr1:40418616
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0145others(6): Show | 17 | HG00544.hp2 HG00735.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1164+1520A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40418616 | ||||||
chr1:40419017
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1164+1921G>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419017 | ||||||
chr1:40419026
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1164+1930C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419026 | ||||||
chr1:40419041
|
A | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 221 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1164+1945A>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419041 | ||||||
chr1:40419280
|
CT | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 268 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1164+2202delT | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 40419280 | |||||
chr1:40419280
|
CTT | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0167a0001c0001t0001g0174others(4): Show | 8 | HG01515.hp2 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1164+2201_1164+220 others(6): Show |
SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 40419280 | |||||
chr1:40419285
|
T | A | 3 | a0002c0004t0004g0025a0002c0004t0004g0246a0002c0004t0004g0247 | 4 | HG01891.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+2189T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419285 | ||||||
chr1:40419334
|
G | T | 1 | a0001c0001t0001g0190 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1164+2238G>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419334 | ||||||
chr1:40419624
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1165-2352A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40419624 | ||||||
chr1:40420082
|
C | T | 3 | a0001c0005t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101 | 3 | HG01433.hp1 HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1165-1894C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420082 | ||||||
chr1:40420160
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0014others(81): Show | 102 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1165-1816A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420160 | ||||||
chr1:40420460
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1165-1516C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420460 | ||||||
chr1:40420631
|
G | A | 1 | a0001c0002t0001g0298 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1165-1345G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420631 | ||||||
chr1:40420819
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1165-1157T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420819 | ||||||
chr1:40420925
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1165-1051A>G | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420925 | ||||||
chr1:40420943
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1165-1033T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420943 | ||||||
chr1:40420985
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0156 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1165-991C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420985 | ||||||
chr1:40420991
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1165-985T>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40420991 | ||||||
chr1:40421367
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0131 | 3 | HG02622.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1165-609C>T | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40421367 | ||||||
chr1:40421511
|
T | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0257others(1): Show | 7 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1165-465T>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40421511 | ||||||
chr1:40421701
|
A | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0257others(2): Show | 8 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165-275A>C | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40421701 | ||||||
chr1:40421717
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0215 | 2 | NA18988.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1165-259G>A | SMAP2 | ENSG00000084070.12 | transcript | ENST00000372718.8 | protein_coding | 9/9 | chr1 | 40421717 |