geneid | 84250 |
---|---|
ensemblid | ENSG00000133302.13 |
hgncid | 25408 |
symbol | SLF1 |
name | SMC5-SMC6 complex localization factor 1 |
refseq_nuc | NM_032290.4 |
refseq_prot | NP_115666.2 |
ensembl_nuc | ENST00000265140.10 |
ensembl_prot | ENSP00000265140.5 |
mane_status | MANE Select |
chr | chr5 |
start | 94618669 |
end | 94697621 |
strand | + |
ver | v1.2 |
region | chr5:94618669-94697621 |
region5000 | chr5:94613669-94702621 |
regionname0 | SLF1_chr5_94618669_94697621 |
regionname5000 | SLF1_chr5_94613669_94702621 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1058 | 255 | 65 | 36 | 115 | 8 | 29 | 89 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0002 | 0/0 | 1058 | 102 | 15 | 17 | 57 | 4 | 9 | 47 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0003 | 0/0 | 1058 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0004 | 0/0 | 89 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0005 | 0/0 | 1058 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0006 | 0/0 | 1058 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0007 | 0/0 | 1058 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0008 | 0/0 | 1058 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 3177 | 245 | 62 | 34 | 115 | 7 | 25 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0002 | 0/0 | 3177 | 102 | 15 | 17 | 57 | 4 | 9 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0003 | 0/0 | 3177 | 3 | 0 | 1 | 0 | 0 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0004 | 0/0 | 3177 | 2 | 0 | 0 | 0 | 0 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0005 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0006 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0007 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0008 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0009 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0010 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0011 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0012 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0013 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
c0014 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2407 | 111 | 19 | 15 | 59 | 2 | 15 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0002 | 0/0 | 2407 | 71 | 12 | 8 | 46 | 1 | 4 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0003 | 0/0 | 2403 | 53 | 26 | 11 | 6 | 3 | 7 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0004 | 0/0 | 2407 | 53 | 3 | 1 | 46 | 0 | 3 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0005 | 0/0 | 2407 | 24 | 3 | 5 | 10 | 1 | 5 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0006 | 1/0 | 2407 | 13 | 0 | 6 | 1 | 3 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0007 | 0/0 | 2407 | 8 | 8 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0008 | 0/0 | 2407 | 4 | 0 | 2 | 0 | 2 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0009 | 0/0 | 2407 | 3 | 0 | 3 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0010 | 0/0 | 2407 | 3 | 3 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0011 | 0/0 | 2407 | 2 | 0 | 0 | 0 | 0 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0012 | 0/0 | 2407 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0013 | 0/0 | 2407 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0014 | 0/0 | 2407 | 2 | 0 | 2 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0015 | 0/0 | 2407 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0016 | 0/0 | 2407 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0017 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0018 | 0/0 | 2407 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0019 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0020 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0021 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0022 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0023 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0024 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
t0025 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3177 | 245 | 62 | 34 | 115 | 7 | 25 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0003 | 0/0 | 3177 | 3 | 0 | 1 | 0 | 0 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0004 | 0/0 | 3177 | 2 | 0 | 0 | 0 | 0 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0005 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0008 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0009 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0011 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0002c0002 | 0/0 | 3177 | 102 | 15 | 17 | 57 | 4 | 9 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0003c0006 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0004c0007 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0005c0010 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0006c0012 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0007c0013 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0008c0014 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5583 | 105 | 17 | 14 | 58 | 2 | 13 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0002 | 0/0 | 5583 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0003 | 0/0 | 5579 | 52 | 25 | 11 | 6 | 3 | 7 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0004 | 0/0 | 5583 | 48 | 1 | 1 | 45 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0005 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0006 | 1/0 | 5583 | 10 | 0 | 5 | 1 | 2 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0007 | 0/0 | 5583 | 8 | 8 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0010 | 0/0 | 5583 | 3 | 3 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0011 | 0/0 | 5583 | 2 | 0 | 0 | 0 | 0 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0012 | 0/0 | 5583 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0014 | 0/0 | 5583 | 2 | 0 | 2 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0015 | 0/0 | 5583 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0016 | 0/0 | 5583 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0017 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0018 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0019 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0021 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0024 | 0/0 | 5583 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0001t0025 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0003t0001 | 0/0 | 5583 | 3 | 0 | 1 | 0 | 0 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0004t0004 | 0/0 | 5583 | 2 | 0 | 0 | 0 | 0 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0005t0004 | 0/0 | 5583 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0008t0006 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0009t0003 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0001c0011t0006 | 0/0 | 5583 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0002c0002t0002 | 0/0 | 5583 | 69 | 12 | 8 | 44 | 1 | 4 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0002c0002t0005 | 0/0 | 5583 | 23 | 3 | 5 | 9 | 1 | 5 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0002c0002t0008 | 0/0 | 5583 | 4 | 0 | 2 | 0 | 2 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0002c0002t0009 | 0/0 | 5583 | 2 | 0 | 2 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0002c0002t0013 | 0/0 | 5583 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0002c0002t0020 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0002c0002t0022 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0003c0006t0001 | 0/0 | 5583 | 2 | 2 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0004c0007t0009 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0005c0010t0001 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0006c0012t0006 | 0/0 | 5583 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0007c0013t0023 | 0/0 | 5583 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
a0008c0014t0004 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | copy fasta | chr5 | 94613669 | 94702621 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0006g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0011g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0011g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0014g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0014g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0015g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0015g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0016g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0017g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0018g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0019g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0024g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0001t0025g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0004t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0004t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0005t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0005t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0008t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0009t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0001c0011t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0008g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0008g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0008g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0009g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0009g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0013g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0013g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0020g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0002c0002t0022g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0003c0006t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0003c0006t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0004c0007t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0005c0010t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0006c0012t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0007c0013t0023g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
a0008c0014t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0241 | EUR | GBR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00140 | hp1 | a0001 | c0001 | t0006 | g0164 | EUR | GBR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00140 | hp2 | a0002 | c0002 | t0005 | g0013 | EUR | GBR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00280 | hp1 | a0001 | c0011 | t0006 | g0128 | EUR | FIN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00639 | hp1 | a0002 | c0002 | t0009 | g0239 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00642 | hp1 | a0002 | c0002 | t0008 | g0012 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00642 | hp2 | a0001 | c0001 | t0014 | g0143 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00673 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00673 | hp2 | a0002 | c0002 | t0013 | g0263 | EAS | CHS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00733 | hp1 | a0001 | c0008 | t0006 | g0157 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0168 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0166 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01081 | hp2 | a0001 | c0001 | t0014 | g0140 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01099 | hp2 | a0002 | c0002 | t0005 | g0309 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01106 | hp1 | a0004 | c0007 | t0009 | g0243 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0292 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0163 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01175 | hp2 | a0001 | c0001 | t0018 | g0132 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0256 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0165 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01261 | hp1 | a0002 | c0002 | t0009 | g0240 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01346 | hp1 | a0002 | c0002 | t0005 | g0311 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01358 | hp2 | a0002 | c0002 | t0008 | g0258 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0167 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01433 | hp1 | a0002 | c0002 | t0005 | g0013 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0259 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01496 | hp1 | a0002 | c0002 | t0005 | g0306 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0118 | EUR | IBS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0174 | EUR | IBS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01516 | hp1 | a0002 | c0002 | t0008 | g0012 | EUR | IBS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0072 | EUR | IBS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0117 | EUR | IBS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01517 | hp2 | a0002 | c0002 | t0008 | g0287 | EUR | IBS | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01891 | hp1 | a0001 | c0005 | t0004 | g0284 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0185 | AMR | PEL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PEL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01978 | hp1 | a0002 | c0002 | t0005 | g0310 | AMR | PEL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0235 | AMR | PEL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0289 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02071 | hp1 | a0002 | c0002 | t0013 | g0264 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02132 | hp1 | a0002 | c0002 | t0005 | g0308 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CDX | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | CDX | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | CDX | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | CDX | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0191 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02258 | hp1 | a0002 | c0002 | t0005 | g0301 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0199 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PEL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02602 | hp1 | a0006 | c0012 | t0006 | g0175 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0291 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0197 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02683 | hp1 | a0001 | c0001 | t0024 | g0141 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02698 | hp2 | a0001 | c0004 | t0004 | g0060 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02717 | hp2 | a0003 | c0006 | t0001 | g0129 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02723 | hp1 | a0001 | c0001 | t0025 | g0192 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02735 | hp1 | a0001 | c0004 | t0004 | g0024 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0074 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0278 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02895 | hp1 | a0003 | c0006 | t0001 | g0130 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0294 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0272 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0293 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0276 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ESN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02922 | hp2 | a0001 | c0001 | t0010 | g0067 | AFR | ESN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02970 | hp1 | a0001 | c0001 | t0010 | g0065 | AFR | ESN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ESN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0189 | AFR | ESN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | ESN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03017 | hp2 | a0007 | c0013 | t0023 | g0269 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0198 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ESN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03139 | hp2 | a0001 | c0001 | t0010 | g0066 | AFR | ESN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03209 | hp2 | a0001 | c0001 | t0012 | g0190 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0195 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03239 | hp2 | a0001 | c0001 | t0011 | g0059 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0194 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0277 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0162 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0224 | AFR | ESN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03516 | hp2 | a0001 | c0001 | t0015 | g0282 | AFR | ESN | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03540 | hp1 | a0002 | c0002 | t0005 | g0298 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03579 | hp1 | a0001 | c0001 | t0015 | g0281 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03654 | hp1 | a0002 | c0002 | t0005 | g0304 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0176 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03669 | hp2 | a0001 | c0001 | t0011 | g0027 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03688 | hp1 | a0001 | c0003 | t0001 | g0179 | SAS | STU | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0257 | SAS | STU | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03704 | hp1 | a0002 | c0002 | t0005 | g0313 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03831 | hp1 | a0002 | c0002 | t0005 | g0303 | SAS | BEB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | BEB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03927 | hp1 | a0002 | c0002 | t0005 | g0305 | SAS | BEB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03942 | hp1 | a0002 | c0002 | t0005 | g0300 | SAS | BEB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | STU | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0221 | SAS | STU | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | STU | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0009 | SAS | STU | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | YRI | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | CHB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | CHB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18906 | hp1 | a0002 | c0002 | t0002 | g0279 | AFR | YRI | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18906 | hp2 | a0001 | c0009 | t0003 | g0113 | AFR | YRI | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18942 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18972 | hp2 | a0002 | c0002 | t0005 | g0297 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18982 | hp2 | a0002 | c0002 | t0005 | g0119 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18983 | hp2 | a0008 | c0014 | t0004 | g0032 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18985 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18987 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18991 | hp2 | a0001 | c0001 | t0017 | g0286 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18992 | hp1 | a0002 | c0002 | t0005 | g0295 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19003 | hp2 | a0002 | c0002 | t0005 | g0314 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19005 | hp1 | a0002 | c0002 | t0020 | g0254 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19011 | hp2 | a0002 | c0002 | t0005 | g0315 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | LWK | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19043 | hp1 | a0001 | c0001 | t0019 | g0270 | AFR | LWK | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | LWK | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19056 | hp1 | a0002 | c0002 | t0005 | g0296 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19063 | hp1 | a0002 | c0002 | t0005 | g0302 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19067 | hp2 | a0002 | c0002 | t0022 | g0312 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19068 | hp1 | a0002 | c0002 | t0005 | g0307 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19072 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19072 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19077 | hp1 | a0005 | c0010 | t0001 | g0339 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0245 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | YRI | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA19240 | hp2 | a0002 | c0002 | t0005 | g0299 | AFR | YRI | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA20129 | hp1 | a0001 | c0005 | t0004 | g0283 | AFR | ASW | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0273 | AFR | ASW | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0120 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03471 | hp1 | a0001 | c0001 | t0016 | g0193 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | USA | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0274 | AFR | USA | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0275 | AFR | USA | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | USA | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0206 | REF | REF | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0186 | REF | REF | SLF1_chr5_94613669_94702621 | SLF1 | chr5 | 94613669 | 94702621 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:94630581
|
G | A | 1 | a0004 | 1 | HG01106.hp1 | stop_gained | HIGH | c.269G>A | p.Trp90* | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/21 | 366/5583 | 269/3177 | 90/1058 | chr5 | 94630581 | ||
chr5:94649476
|
A | G | 1 | a0008 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.617A>G | p.Asp206Gly | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/21 | 714/5583 | 617/3177 | 206/1058 | chr5 | 94649476 | ||
chr5:94649596
|
A | G | 1 | a0007 | 1 | HG03017.hp2 | missense_variant&splice_region_variant | MODERATE | c.737A>G | p.Gln246Arg | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/21 | 834/5583 | 737/3177 | 246/1058 | chr5 | 94649596 | ||
chr5:94651827
|
C | A | 2 | a0002a0004 | 103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
missense_variant | MODERATE | c.864C>A | p.Ser288Arg | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/21 | 961/5583 | 864/3177 | 288/1058 | chr5 | 94651827 | ||
chr5:94666020
|
A | G | 1 | a0006 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1528A>G | p.Ile510Val | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/21 | 1625/5583 | 1528/3177 | 510/1058 | chr5 | 94666020 | ||
chr5:94686711
|
A | G | 1 | a0003 | 2 | HG02717.hp2 HG02895.hp1 |
missense_variant | MODERATE | c.2114A>G | p.Gln705Arg | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/21 | 2211/5583 | 2114/3177 | 705/1058 | chr5 | 94686711 | ||
chr5:94695113
|
G | A | 1 | a0005 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.2978G>A | p.Cys993Tyr | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 3075/5583 | 2978/3177 | 993/1058 | chr5 | 94695113 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:94629103
|
T | C | 1 | a0001c0003 | 3 | HG01361.hp2 HG03490.hp2 HG03688.hp1 |
synonymous_variant | LOW | c.126T>C | p.Asn42Asn | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 3/21 | 223/5583 | 126/3177 | 42/1058 | chr5 | 94629103 | ||
chr5:94665950
|
G | A | 1 | a0001c0008 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.1458G>A | p.Ser486Ser | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/21 | 1555/5583 | 1458/3177 | 486/1058 | chr5 | 94665950 | ||
chr5:94670208
|
G | A | 1 | a0001c0009 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1590G>A | p.Lys530Lys | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 13/21 | 1687/5583 | 1590/3177 | 530/1058 | chr5 | 94670208 | ||
chr5:94694970
|
A | G | 1 | a0001c0011 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.2835A>G | p.Lys945Lys | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 2932/5583 | 2835/3177 | 945/1058 | chr5 | 94694970 | ||
chr5:94694985
|
G | A | 1 | a0001c0004 | 2 | HG02698.hp2 HG02735.hp1 |
synonymous_variant | LOW | c.2850G>A | p.Gln950Gln | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 2947/5583 | 2850/3177 | 950/1058 | chr5 | 94694985 | ||
chr5:94695093
|
A | G | 1 | a0001c0005 | 2 | HG01891.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.2958A>G | p.Leu986Leu | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 3055/5583 | 2958/3177 | 986/1058 | chr5 | 94695093 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:94618683
|
T | A | 1 | a0001c0001t0017 | 1 | NA18991.hp2 | 5_prime_UTR_variant | MODIFIER | c.-83T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/21 | 10128 | chr5 | 94618683 | |||||
chr5:94618684
|
C | A | 1 | a0001c0001t0018 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/21 | 10127 | chr5 | 94618684 | |||||
chr5:94695380
|
C | G | 1 | a0001c0001t0025 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 68 | chr5 | 94695380 | |||||
chr5:94695415
|
A | G | 1 | a0001c0001t0016 | 2 | HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*103A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 103 | chr5 | 94695415 | |||||
chr5:94695458
|
A | T | 1 | a0001c0001t0024 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 146 | chr5 | 94695458 | |||||
chr5:94695539
|
TG | T | 1 | a0001c0001t0010 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*228delG | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 228 | chr5 | 94695539 | |||||
chr5:94695840
|
AAAAT | A | 2 | a0001c0001t0003a0001c0009t0003 | 53 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*532_*535delTAAA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 532 | INFO_REALIGN_3_PRIME | chr5 | 94695840 | ||||
chr5:94695925
|
A | G | 1 | a0001c0001t0010 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*613A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 613 | chr5 | 94695925 | |||||
chr5:94695966
|
G | A | 1 | a0001c0001t0011 | 2 | HG03239.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*654G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 654 | chr5 | 94695966 | |||||
chr5:94696177
|
G | A | 1 | a0001c0001t0019 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 865 | chr5 | 94696177 | |||||
chr5:94696287
|
A | T | 1 | a0001c0001t0015 | 2 | HG03516.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*975A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 975 | chr5 | 94696287 | |||||
chr5:94696288
|
A | G | 1 | a0002c0002t0008 | 4 | HG00642.hp1 HG01358.hp2 HG01516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*976A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 976 | chr5 | 94696288 | |||||
chr5:94696298
|
T | G | 1 | a0002c0002t0020 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*986T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 986 | chr5 | 94696298 | |||||
chr5:94696371
|
C | CT | 1 | a0001c0001t0010 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1060dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1061 | INFO_REALIGN_3_PRIME | chr5 | 94696371 | ||||
chr5:94696406
|
G | A | 1 | a0001c0001t0021 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1094G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1094 | chr5 | 94696406 | |||||
chr5:94696417
|
T | C | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
3_prime_UTR_variant | MODIFIER | c.*1105T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1105 | chr5 | 94696417 | |||||
chr5:94696511
|
A | C | 3 | a0002c0002t0008a0002c0002t0009a0004c0007t0009 | 7 | HG00639.hp1 HG00642.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1199A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1199 | chr5 | 94696511 | |||||
chr5:94696559
|
G | A | 6 | a0001c0001t0004a0001c0001t0011a0001c0001t0017others(3): Show | 56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1247G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1247 | chr5 | 94696559 | |||||
chr5:94696702
|
A | G | 1 | a0001c0001t0019 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1390A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1390 | chr5 | 94696702 | |||||
chr5:94696706
|
T | A | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1394T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1394 | chr5 | 94696706 | |||||
chr5:94696712
|
T | C | 1 | a0002c0002t0013 | 2 | HG00673.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1400T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1400 | chr5 | 94696712 | |||||
chr5:94697073
|
A | G | 1 | a0007c0013t0023 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1761A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1761 | chr5 | 94697073 | |||||
chr5:94697284
|
C | T | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(23): Show | 235 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1972C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1972 | chr5 | 94697284 | |||||
chr5:94697290
|
G | T | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(21): Show | 226 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*1978G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 1978 | chr5 | 94697290 | |||||
chr5:94697464
|
T | G | 7 | a0001c0001t0002a0002c0002t0002a0002c0002t0008others(4): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2152T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 2152 | chr5 | 94697464 | |||||
chr5:94697519
|
C | T | 3 | a0001c0001t0014a0001c0001t0018a0001c0001t0024 | 4 | HG00642.hp2 HG01081.hp2 HG01175.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2207C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 2207 | chr5 | 94697519 | |||||
chr5:94697534
|
A | G | 1 | a0002c0002t0022 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2222A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 21/21 | 2222 | chr5 | 94697534 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:94618850
|
C | T | 1 | a0001c0001t0003g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1+85C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94618850 | ||||||
chr5:94619029
|
A | G | 1 | a0001c0001t0001g0344 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-1+264A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94619029 | ||||||
chr5:94619263
|
G | T | 28 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(25): Show | 28 | HG00423.hp1 HG01071.hp2 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.-1+498G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94619263 | ||||||
chr5:94619286
|
A | AT | 26 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(23): Show | 27 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-1+533dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94619286 | |||||
chr5:94619286
|
AT | A | 54 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0316others(51): Show | 56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-1+533delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94619286 | |||||
chr5:94619427
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-1+662C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94619427 | ||||||
chr5:94619508
|
G | C | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+743G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94619508 | ||||||
chr5:94619573
|
G | T | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1+808G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94619573 | ||||||
chr5:94619611
|
TTTG | T | 57 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(54): Show | 58 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(55): Show |
intron_variant | MODIFIER | c.-1+859_-1+861delTT others(1): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94619611 | |||||
chr5:94620102
|
A | G | 1 | a0002c0002t0002g0288 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-1+1337A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620102 | ||||||
chr5:94620192
|
A | G | 2 | a0002c0002t0008g0012a0002c0002t0008g0287 | 3 | HG00642.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-1+1427A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620192 | ||||||
chr5:94620246
|
A | G | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+1481A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620246 | ||||||
chr5:94620278
|
C | A | 4 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(1): Show | 4 | HG01167.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+1513C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620278 | ||||||
chr5:94620361
|
C | T | 55 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(52): Show | 57 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-1+1596C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620361 | ||||||
chr5:94620420
|
C | T | 4 | a0001c0001t0003g0115a0001c0001t0003g0116a0001c0001t0003g0117others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+1655C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620420 | ||||||
chr5:94620454
|
G | A | 28 | a0001c0001t0007g0120a0002c0002t0002g0291a0002c0002t0002g0292others(25): Show | 29 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1+1689G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620454 | ||||||
chr5:94620597
|
A | G | 1 | a0002c0002t0002g0280 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-1+1832A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620597 | ||||||
chr5:94620611
|
A | C | 8 | a0002c0002t0002g0272a0002c0002t0002g0273a0002c0002t0002g0274others(5): Show | 8 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+1846A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620611 | ||||||
chr5:94620853
|
T | C | 1 | a0001c0001t0004g0022 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-1+2088T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620853 | ||||||
chr5:94620905
|
A | G | 1 | a0002c0002t0002g0271 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-1+2140A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620905 | ||||||
chr5:94620931
|
C | G | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1+2166C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94620931 | ||||||
chr5:94621083
|
A | T | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-1+2318A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94621083 | ||||||
chr5:94621098
|
T | C | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+2333T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94621098 | ||||||
chr5:94621134
|
C | T | 67 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(64): Show | 77 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.-1+2369C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94621134 | ||||||
chr5:94621161
|
G | A | 27 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(24): Show | 28 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+2396G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94621161 | ||||||
chr5:94621201
|
T | C | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1+2436T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94621201 | ||||||
chr5:94621232
|
A | G | 25 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0200others(22): Show | 25 | HG00558.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-1+2467A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94621232 | ||||||
chr5:94621281
|
A | G | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.-1+2516A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94621281 | ||||||
chr5:94621371
|
A | G | 4 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(1): Show | 4 | HG01167.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+2606A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94621371 | ||||||
chr5:94621598
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-1+2833T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94621598 | ||||||
chr5:94621767
|
C | G | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.-1+3002C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94621767 | ||||||
chr5:94621883
|
T | TAC | 56 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(53): Show | 57 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-1+3140_-1+3141dup others(2): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94621883 | |||||
chr5:94621883
|
T | TACAC | 4 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(1): Show | 4 | HG01099.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+3138_-1+3141dup others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94621883 | |||||
chr5:94621883
|
TAC | T | 88 | a0001c0001t0001g0021a0001c0001t0001g0220a0001c0001t0004g0004others(85): Show | 91 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-1+3140_-1+3141del others(2): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94621883 | |||||
chr5:94621883
|
TACAC | T | 79 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0114others(76): Show | 89 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.-1+3138_-1+3141del others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94621883 | |||||
chr5:94622126
|
A | G | 67 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(64): Show | 77 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.-1+3361A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94622126 | ||||||
chr5:94622262
|
G | A | 27 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(24): Show | 28 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+3497G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94622262 | ||||||
chr5:94622353
|
A | C | 27 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(24): Show | 28 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+3588A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94622353 | ||||||
chr5:94622465
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-1+3700A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94622465 | ||||||
chr5:94622551
|
A | G | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-1+3786A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94622551 | ||||||
chr5:94622630
|
A | C | 7 | a0002c0002t0002g0011a0002c0002t0002g0265a0002c0002t0002g0266others(4): Show | 8 | HG00673.hp2 HG02071.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+3865A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94622630 | ||||||
chr5:94622661
|
G | C | 27 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(24): Show | 28 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+3896G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94622661 | ||||||
chr5:94622702
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-1+3937G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94622702 | ||||||
chr5:94622828
|
G | A | 27 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(24): Show | 28 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+4063G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94622828 | ||||||
chr5:94623215
|
T | C | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1+4450T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623215 | ||||||
chr5:94623240
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-1+4475G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623240 | ||||||
chr5:94623244
|
C | G | 27 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(24): Show | 28 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+4479C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623244 | ||||||
chr5:94623269
|
G | A | 27 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(24): Show | 28 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+4504G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623269 | ||||||
chr5:94623336
|
A | C | 1 | a0001c0001t0010g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-1+4571A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623336 | ||||||
chr5:94623460
|
G | A | 27 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(24): Show | 28 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+4695G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623460 | ||||||
chr5:94623582
|
T | C | 1 | a0002c0002t0013g0263 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-1+4817T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623582 | ||||||
chr5:94623584
|
A | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-1+4819A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623584 | ||||||
chr5:94623717
|
G | T | 2 | a0002c0002t0002g0011a0002c0002t0002g0268 | 3 | HG02083.hp1 NA18971.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.-1+4952G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623717 | ||||||
chr5:94623761
|
A | G | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-1+4996A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623761 | ||||||
chr5:94623797
|
T | C | 1 | a0001c0004t0004g0024 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1-5014T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623797 | ||||||
chr5:94623872
|
A | G | 1 | a0002c0002t0002g0262 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1-4939A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623872 | ||||||
chr5:94623990
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1-4821G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94623990 | ||||||
chr5:94624579
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1-4232G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94624579 | ||||||
chr5:94624998
|
A | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1-3813A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94624998 | ||||||
chr5:94625060
|
G | T | 55 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(52): Show | 57 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1-3751G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625060 | ||||||
chr5:94625134
|
A | G | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1-3677A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625134 | ||||||
chr5:94625159
|
C | T | 1 | a0001c0001t0025g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1-3652C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625159 | ||||||
chr5:94625171
|
C | T | 1 | a0001c0001t0004g0064 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1-3640C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625171 | ||||||
chr5:94625192
|
C | CA | 11 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG00741.hp2 HG01175.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1-3602dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94625192 | |||||
chr5:94625192
|
CA | C | 53 | a0001c0001t0001g0187a0001c0001t0003g0006a0001c0001t0003g0068others(50): Show | 54 | HG00639.hp2 HG00741.hp1 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.1-3602delA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94625192 | |||||
chr5:94625202
|
A | AT | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1-3609_1-3608insT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625202 | ||||||
chr5:94625206
|
A | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1-3605A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625206 | ||||||
chr5:94625210
|
T | A | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1-3601T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625210 | ||||||
chr5:94625266
|
C | T | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | NA18940.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1-3545C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625266 | ||||||
chr5:94625346
|
A | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1-3465A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625346 | ||||||
chr5:94625378
|
A | G | 7 | a0002c0002t0002g0011a0002c0002t0002g0265a0002c0002t0002g0266others(4): Show | 8 | HG00673.hp2 HG02071.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-3433A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625378 | ||||||
chr5:94625508
|
C | T | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1-3303C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625508 | ||||||
chr5:94625571
|
T | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1-3240T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625571 | ||||||
chr5:94625714
|
T | G | 1 | a0002c0002t0002g0221 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1-3097T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625714 | ||||||
chr5:94625867
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0220 | 2 | NA18964.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1-2944T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625867 | ||||||
chr5:94625992
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1-2819C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94625992 | ||||||
chr5:94626020
|
G | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1-2791G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626020 | ||||||
chr5:94626063
|
C | A | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1-2748C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626063 | ||||||
chr5:94626097
|
C | CA | 98 | a0001c0001t0001g0200a0001c0001t0002g0227a0001c0001t0002g0255others(95): Show | 109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1-2705dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94626097 | |||||
chr5:94626099
|
A | G | 1 | a0001c0001t0004g0063 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1-2712A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626099 | ||||||
chr5:94626159
|
C | A | 345 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0020others(342): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1-2652C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626159 | ||||||
chr5:94626189
|
C | T | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1-2622C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626189 | ||||||
chr5:94626252
|
C | CA | 13 | a0001c0001t0001g0322a0001c0001t0003g0072a0001c0001t0003g0075others(10): Show | 13 | HG00423.hp2 HG00735.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-2541dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94626252 | |||||
chr5:94626252
|
CA | C | 9 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(6): Show | 9 | HG00099.hp1 HG01168.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1-2541delA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94626252 | |||||
chr5:94626556
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0001g0180others(1): Show | 4 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-2255A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626556 | ||||||
chr5:94626565
|
A | C | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1-2246A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626565 | ||||||
chr5:94626707
|
T | G | 2 | a0001c0001t0007g0194a0001c0001t0007g0195 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1-2104T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626707 | ||||||
chr5:94626794
|
T | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1-2017T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626794 | ||||||
chr5:94626816
|
T | A | 28 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(25): Show | 28 | HG00423.hp1 HG01071.hp2 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.1-1995T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626816 | ||||||
chr5:94626880
|
G | A | 1 | a0002c0002t0002g0261 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1-1931G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626880 | ||||||
chr5:94626930
|
A | G | 1 | a0001c0003t0001g0179 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1-1881A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94626930 | ||||||
chr5:94627330
|
G | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1-1481G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627330 | ||||||
chr5:94627351
|
G | A | 1 | a0002c0002t0002g0291 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1-1460G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627351 | ||||||
chr5:94627366
|
C | T | 1 | a0001c0001t0003g0112 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1-1445C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627366 | ||||||
chr5:94627565
|
C | G | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1-1246C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627565 | ||||||
chr5:94627585
|
C | CAT | 20 | a0001c0001t0001g0213a0001c0001t0001g0220a0001c0001t0001g0290others(17): Show | 20 | HG00673.hp1 HG01515.hp2 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-1192_1-1191dupTA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
C | CATAT | 8 | a0001c0001t0001g0177a0001c0001t0001g0184a0001c0001t0001g0214others(5): Show | 9 | HG01071.hp2 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1-1194_1-1191dupTA others(2): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
C | CATATAT | 17 | a0001c0001t0001g0007a0001c0001t0001g0215a0001c0001t0001g0216others(14): Show | 18 | HG01071.hp1 HG01074.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1-1196_1-1191dupTA others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
C | CATATATA others(1): Show |
8 | a0001c0001t0001g0178a0001c0001t0001g0317a0001c0001t0001g0337others(5): Show | 8 | HG00741.hp1 HG02040.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-1198_1-1191dupTA others(6): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
C | CATATATA others(3): Show |
11 | a0001c0001t0001g0338a0001c0001t0003g0070a0001c0001t0003g0074others(8): Show | 11 | HG00423.hp1 HG01099.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1-1200_1-1191dupTA others(8): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
C | CATATATA others(5): Show |
14 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0098others(11): Show | 14 | HG01175.hp1 HG01361.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1-1202_1-1191dupTA others(10): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
C | CATATATA others(7): Show |
8 | a0001c0001t0001g0340a0001c0001t0003g0072a0001c0001t0003g0105others(5): Show | 8 | HG01257.hp2 HG01516.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-1204_1-1191dupTA others(12): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
C | CATATATA others(9): Show |
4 | a0001c0001t0003g0109a0001c0001t0003g0110a0001c0001t0007g0191others(1): Show | 4 | HG01358.hp1 HG02257.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-1206_1-1191dupTA others(14): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
C | CATATATA others(11): Show |
3 | a0001c0001t0003g0111a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG01515.hp1 HG01517.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1-1208_1-1191dupTA others(16): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
C | CATATATA others(13): Show |
2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG01975.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1-1210_1-1191dupTA others(18): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
CAT | C | 24 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0001g0158others(21): Show | 24 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1-1192_1-1191delTA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
CATAT | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(27): Show | 33 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1-1194_1-1191delTA others(2): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
CATATAT | C | 8 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0014g0140others(5): Show | 8 | HG00642.hp2 HG01081.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-1196_1-1191delTA others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
CATATATA others(1): Show |
C | 3 | a0001c0001t0003g0079a0001c0001t0003g0080a0001c0001t0003g0081 | 3 | HG01261.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1-1198_1-1191delTA others(6): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
CATATATA others(5): Show |
C | 2 | a0001c0001t0004g0023a0001c0001t0004g0061 | 2 | NA18965.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1-1202_1-1191delTA others(10): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
CATATATA others(7): Show |
C | 48 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(45): Show | 50 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1-1204_1-1191delTA others(12): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
CATATATA others(9): Show |
C | 3 | a0001c0001t0011g0027a0001c0005t0004g0283a0001c0005t0004g0284 | 3 | HG01891.hp1 HG03669.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-1206_1-1191delTA others(14): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
CATATATA others(11): Show |
C | 3 | a0001c0001t0003g0071a0001c0001t0003g0077a0001c0001t0003g0078 | 3 | HG01891.hp2 HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1-1208_1-1191delTA others(16): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
CATATATA others(15): Show |
C | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1-1212_1-1191delTA others(20): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627585
|
CATATATA others(19): Show |
C | 1 | a0001c0001t0003g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1-1216_1-1191delTA others(24): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627585 | |||||
chr5:94627588
|
A | ATATATG | 5 | a0002c0002t0002g0279a0002c0002t0005g0119a0002c0002t0005g0313others(2): Show | 5 | HG03704.hp1 NA18906.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-1218_1-1217insGT others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627588 | |||||
chr5:94627590
|
A | ATATG | 18 | a0002c0002t0002g0259a0002c0002t0002g0272a0002c0002t0002g0273others(15): Show | 19 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1-1218_1-1217insGT others(2): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627590 | |||||
chr5:94627592
|
A | ATG | 14 | a0001c0001t0002g0255a0002c0002t0002g0221a0002c0002t0002g0223others(11): Show | 15 | HG00642.hp1 HG00735.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1-1218_1-1217insGT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627592 | |||||
chr5:94627594
|
A | G | 49 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(46): Show | 58 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1-1217A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627594 | ||||||
chr5:94627596
|
A | G | 8 | a0002c0002t0002g0224a0002c0002t0002g0265a0002c0002t0002g0266others(5): Show | 8 | HG01167.hp1 HG02622.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-1215A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627596 | ||||||
chr5:94627656
|
A | T | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1-1155A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627656 | ||||||
chr5:94627833
|
C | CT | 6 | a0001c0001t0003g0074a0001c0001t0003g0104a0001c0004t0004g0024others(3): Show | 6 | HG02698.hp2 HG02735.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-965dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 94627833 | |||||
chr5:94627896
|
C | T | 28 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(25): Show | 28 | HG00423.hp1 HG01071.hp2 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.1-915C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627896 | ||||||
chr5:94627899
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1-912G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627899 | ||||||
chr5:94627953
|
C | A | 1 | a0001c0001t0004g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1-858C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627953 | ||||||
chr5:94627974
|
C | T | 1 | a0001c0001t0011g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1-837C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94627974 | ||||||
chr5:94628007
|
A | G | 7 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0090others(4): Show | 7 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1-804A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94628007 | ||||||
chr5:94628056
|
A | C | 3 | a0002c0002t0002g0251a0002c0002t0002g0252a0002c0002t0002g0271 | 3 | HG02165.hp1 NA18960.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1-755A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94628056 | ||||||
chr5:94628111
|
G | A | 1 | a0002c0002t0002g0291 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1-700G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94628111 | ||||||
chr5:94628233
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0121a0001c0001t0001g0131others(7): Show | 11 | HG01071.hp1 HG01074.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1-578C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94628233 | ||||||
chr5:94628238
|
A | C | 345 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0020others(342): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1-573A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94628238 | ||||||
chr5:94628294
|
A | G | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.1-517A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94628294 | ||||||
chr5:94628304
|
A | G | 67 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(64): Show | 77 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1-507A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94628304 | ||||||
chr5:94628417
|
G | A | 1 | a0002c0002t0002g0221 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1-394G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94628417 | ||||||
chr5:94628596
|
T | A | 1 | a0001c0001t0003g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1-215T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94628596 | ||||||
chr5:94628661
|
T | A | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1-150T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 1/20 | chr5 | 94628661 | ||||||
chr5:94628989
|
A | G | 56 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(53): Show | 58 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.114+65A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 2/20 | chr5 | 94628989 | ||||||
chr5:94629333
|
A | G | 1 | a0001c0001t0006g0185 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.190+166A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 3/20 | chr5 | 94629333 | ||||||
chr5:94629402
|
TTTTG | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.190+239_190+242del others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 94629402 | |||||
chr5:94629414
|
C | CA | 53 | a0001c0001t0001g0337a0001c0001t0004g0004a0001c0001t0004g0005others(50): Show | 55 | HG00558.hp1 HG00621.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.190+257dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 94629414 | |||||
chr5:94629414
|
CA | C | 95 | a0001c0001t0001g0173a0001c0001t0002g0227a0001c0001t0002g0255others(92): Show | 106 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.190+257delA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 94629414 | |||||
chr5:94629567
|
GAAGCAAT others(22): Show |
G | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.190+404_190+432del others(29): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 94629567 | |||||
chr5:94629647
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.190+480C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 3/20 | chr5 | 94629647 | ||||||
chr5:94629957
|
C | T | 3 | a0002c0002t0002g0292a0002c0002t0002g0293a0002c0002t0002g0294 | 3 | HG01167.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.191-546C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 3/20 | chr5 | 94629957 | ||||||
chr5:94630239
|
G | A | 5 | a0001c0001t0007g0120a0001c0001t0007g0196a0001c0001t0007g0197others(2): Show | 5 | HG02258.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-264G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 3/20 | chr5 | 94630239 | ||||||
chr5:94631004
|
C | CA | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.431+267dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94631004 | |||||
chr5:94631044
|
A | T | 209 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(206): Show | 223 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.431+301A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94631044 | ||||||
chr5:94631385
|
A | C | 1 | a0001c0001t0003g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.431+642A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94631385 | ||||||
chr5:94631547
|
A | C | 55 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(52): Show | 57 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.431+804A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94631547 | ||||||
chr5:94631612
|
A | C | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.431+869A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94631612 | ||||||
chr5:94631731
|
C | T | 345 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0020others(342): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.431+988C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94631731 | ||||||
chr5:94631801
|
A | G | 342 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0020others(339): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.431+1058A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94631801 | ||||||
chr5:94631956
|
ATTTTTTT others(15): Show |
A | 28 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(25): Show | 28 | HG00423.hp1 HG01071.hp2 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.431+1223_431+1244d others(24): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94631956 | |||||
chr5:94631974
|
T | C | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.431+1231T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94631974 | ||||||
chr5:94631980
|
TTTTTTTT others(2): Show |
T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.431+1238_431+1246d others(11): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94631980 | ||||||
chr5:94631988
|
TC | T | 56 | a0001c0001t0003g0083a0001c0001t0004g0004a0001c0001t0004g0005others(53): Show | 58 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.431+1247delC | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94631988 | |||||
chr5:94631989
|
C | T | 59 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(56): Show | 60 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(57): Show |
intron_variant | MODIFIER | c.431+1246C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94631989 | ||||||
chr5:94632071
|
C | T | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.431+1328C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94632071 | ||||||
chr5:94632281
|
G | C | 53 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(50): Show | 55 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.431+1538G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94632281 | ||||||
chr5:94632466
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.431+1723A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94632466 | ||||||
chr5:94632787
|
G | T | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.431+2044G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94632787 | ||||||
chr5:94632835
|
G | A | 2 | a0001c0001t0003g0070a0001c0001t0003g0088 | 2 | HG00741.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.431+2092G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94632835 | ||||||
chr5:94632910
|
T | C | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.431+2167T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94632910 | ||||||
chr5:94632940
|
C | T | 1 | a0002c0002t0005g0303 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.431+2197C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94632940 | ||||||
chr5:94633027
|
G | C | 1 | a0001c0001t0006g0185 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.431+2284G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94633027 | ||||||
chr5:94633047
|
G | A | 208 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(205): Show | 222 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.431+2304G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94633047 | ||||||
chr5:94633130
|
G | A | 1 | a0001c0001t0007g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.431+2387G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94633130 | ||||||
chr5:94633148
|
C | T | 4 | a0001c0001t0012g0189a0001c0001t0012g0190a0002c0002t0002g0249others(1): Show | 4 | HG00621.hp1 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+2405C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94633148 | ||||||
chr5:94633192
|
G | A | 1 | a0001c0001t0004g0057 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.431+2449G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94633192 | ||||||
chr5:94633215
|
G | A | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0211others(1): Show | 4 | HG01081.hp1 HG02602.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+2472G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94633215 | ||||||
chr5:94633376
|
A | G | 1 | a0001c0001t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.431+2633A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94633376 | ||||||
chr5:94633392
|
A | G | 1 | a0001c0001t0003g0107 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.431+2649A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94633392 | ||||||
chr5:94633685
|
C | T | 2 | a0002c0002t0002g0222a0002c0002t0002g0248 | 2 | NA18990.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.431+2942C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94633685 | ||||||
chr5:94633756
|
G | A | 1 | a0002c0002t0002g0291 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.431+3013G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94633756 | ||||||
chr5:94634052
|
C | T | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.431+3309C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94634052 | ||||||
chr5:94634168
|
A | G | 1 | a0002c0002t0002g0247 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.431+3425A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94634168 | ||||||
chr5:94634199
|
T | C | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.431+3456T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94634199 | ||||||
chr5:94634366
|
G | A | 7 | a0001c0001t0007g0120a0001c0001t0007g0194a0001c0001t0007g0195others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+3623G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94634366 | ||||||
chr5:94634390
|
C | G | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.431+3647C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94634390 | ||||||
chr5:94634511
|
C | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.431+3768C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94634511 | ||||||
chr5:94634613
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.431+3870C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94634613 | ||||||
chr5:94634707
|
C | A | 55 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(52): Show | 57 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.431+3964C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94634707 | ||||||
chr5:94634960
|
T | G | 2 | a0002c0002t0005g0298a0002c0002t0005g0299 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.431+4217T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94634960 | ||||||
chr5:94634968
|
T | C | 1 | a0001c0001t0003g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.431+4225T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94634968 | ||||||
chr5:94635000
|
C | T | 1 | a0002c0002t0013g0263 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.431+4257C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635000 | ||||||
chr5:94635057
|
C | A | 1 | a0001c0001t0001g0290 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.431+4314C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635057 | ||||||
chr5:94635136
|
C | CCT | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.431+4393_431+4394i others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635136 | ||||||
chr5:94635190
|
A | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.431+4447A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635190 | ||||||
chr5:94635334
|
C | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.431+4591C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635334 | ||||||
chr5:94635337
|
C | CT | 91 | a0001c0001t0001g0020a0001c0001t0001g0127a0001c0001t0001g0137others(88): Show | 93 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.431+4618dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94635337 | |||||
chr5:94635337
|
C | CTT | 12 | a0001c0001t0004g0017a0001c0001t0004g0028a0001c0001t0004g0050others(9): Show | 12 | HG00423.hp2 HG00558.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.431+4617_431+4618d others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94635337 | |||||
chr5:94635337
|
CT | C | 54 | a0001c0001t0001g0144a0001c0001t0001g0325a0001c0001t0002g0227others(51): Show | 62 | HG00408.hp1 HG00621.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.431+4618delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94635337 | |||||
chr5:94635381
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.431+4638C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635381 | ||||||
chr5:94635382
|
C | G | 1 | a0001c0001t0001g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.431+4639C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635382 | ||||||
chr5:94635383
|
ACTCTATG others(4): Show |
A | 1 | a0001c0001t0001g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.431+4641_431+4651d others(13): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635383 | ||||||
chr5:94635388
|
A | G | 1 | a0001c0001t0025g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.431+4645A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635388 | ||||||
chr5:94635550
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.431+4807T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635550 | ||||||
chr5:94635770
|
T | G | 1 | a0002c0002t0002g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.431+5027T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94635770 | ||||||
chr5:94636253
|
C | A | 28 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0003others(25): Show | 32 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.431+5510C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94636253 | ||||||
chr5:94636488
|
G | A | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.431+5745G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94636488 | ||||||
chr5:94636502
|
C | T | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.431+5759C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94636502 | ||||||
chr5:94636552
|
C | G | 113 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(110): Show | 116 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.431+5809C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94636552 | ||||||
chr5:94636580
|
ATTC | A | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.431+5841_431+5843d others(5): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94636580 | |||||
chr5:94636710
|
A | AT | 46 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0001g0152others(43): Show | 46 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.431+5992dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94636710 | |||||
chr5:94636710
|
A | ATT | 30 | a0001c0001t0004g0005a0001c0001t0004g0016a0001c0001t0004g0017others(27): Show | 31 | HG00621.hp2 HG01891.hp1 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.431+5991_431+5992d others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94636710 | |||||
chr5:94636710
|
AT | A | 10 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0139others(7): Show | 10 | HG00438.hp2 HG01255.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.431+5992delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94636710 | |||||
chr5:94636710
|
ATT | A | 43 | a0001c0001t0003g0006a0001c0001t0003g0070a0001c0001t0003g0071others(40): Show | 44 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.431+5991_431+5992d others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94636710 | |||||
chr5:94636710
|
ATTT | A | 6 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0072others(3): Show | 6 | HG01516.hp2 HG02683.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+5990_431+5992d others(5): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94636710 | |||||
chr5:94636710
|
ATTTTT | A | 22 | a0001c0001t0002g0255a0002c0002t0002g0221a0002c0002t0002g0268others(19): Show | 23 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.431+5988_431+5992d others(7): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94636710 | |||||
chr5:94636710
|
ATTTTTT | A | 68 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(65): Show | 78 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.431+5987_431+5992d others(8): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94636710 | |||||
chr5:94636780
|
C | G | 1 | a0001c0001t0006g0185 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.431+6037C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94636780 | ||||||
chr5:94636798
|
ACCT | A | 4 | a0001c0001t0004g0040a0001c0001t0004g0041a0001c0001t0004g0049others(1): Show | 4 | NA18612.hp1 NA18964.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+6065_431+6067d others(5): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94636798 | |||||
chr5:94636805
|
C | T | 1 | a0002c0002t0002g0252 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.431+6062C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94636805 | ||||||
chr5:94636821
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.431+6078G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94636821 | ||||||
chr5:94636931
|
G | A | 1 | a0001c0001t0006g0185 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.431+6188G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94636931 | ||||||
chr5:94637034
|
G | A | 1 | a0001c0011t0006g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.432-6239G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637034 | ||||||
chr5:94637051
|
A | G | 1 | a0001c0001t0003g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.432-6222A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637051 | ||||||
chr5:94637191
|
C | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-6082C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637191 | ||||||
chr5:94637212
|
C | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-6061C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637212 | ||||||
chr5:94637227
|
T | C | 1 | a0001c0001t0007g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.432-6046T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637227 | ||||||
chr5:94637329
|
C | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-5944C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637329 | ||||||
chr5:94637472
|
A | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-5801A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637472 | ||||||
chr5:94637688
|
G | A | 1 | a0001c0001t0004g0042 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.432-5585G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637688 | ||||||
chr5:94637700
|
T | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-5573T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637700 | ||||||
chr5:94637738
|
T | C | 4 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(1): Show | 4 | NA18940.hp2 NA18968.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.432-5535T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637738 | ||||||
chr5:94637776
|
T | TGTTCTGC others(17): Show |
1 | a0001c0001t0001g0322 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.432-5496_432-5473d others(26): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94637776 | |||||
chr5:94637882
|
A | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-5391A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94637882 | ||||||
chr5:94638101
|
T | G | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.432-5172T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638101 | ||||||
chr5:94638128
|
C | T | 53 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(50): Show | 55 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.432-5145C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638128 | ||||||
chr5:94638171
|
C | A | 33 | a0001c0001t0002g0255a0002c0002t0002g0011a0002c0002t0002g0225others(30): Show | 35 | HG00140.hp2 HG00673.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.432-5102C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638171 | ||||||
chr5:94638174
|
C | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-5099C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638174 | ||||||
chr5:94638196
|
T | A | 1 | a0001c0001t0003g0075 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.432-5077T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638196 | ||||||
chr5:94638217
|
C | T | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.432-5056C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638217 | ||||||
chr5:94638240
|
G | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0188a0001c0001t0001g0343 | 3 | HG02293.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.432-5033G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638240 | ||||||
chr5:94638242
|
G | A | 1 | a0001c0001t0004g0031 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.432-5031G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638242 | ||||||
chr5:94638328
|
G | A | 2 | a0001c0005t0004g0283a0001c0005t0004g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.432-4945G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638328 | ||||||
chr5:94638351
|
T | G | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.432-4922T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638351 | ||||||
chr5:94638368
|
A | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-4905A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638368 | ||||||
chr5:94638380
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.432-4893C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638380 | ||||||
chr5:94638413
|
C | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-4860C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638413 | ||||||
chr5:94638419
|
C | A | 1 | a0002c0002t0002g0224 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.432-4854C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638419 | ||||||
chr5:94638538
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.432-4735C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638538 | ||||||
chr5:94638571
|
A | G | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.432-4702A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638571 | ||||||
chr5:94638676
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.432-4597A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638676 | ||||||
chr5:94638676
|
A | T | 2 | a0001c0001t0003g0075a0001c0001t0003g0102 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.432-4597A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638676 | ||||||
chr5:94638764
|
C | T | 1 | a0002c0002t0002g0253 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.432-4509C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638764 | ||||||
chr5:94638787
|
T | C | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.432-4486T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94638787 | ||||||
chr5:94639034
|
T | C | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.432-4239T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639034 | ||||||
chr5:94639037
|
C | CT | 12 | a0001c0001t0001g0161a0001c0001t0001g0181a0001c0001t0001g0183others(9): Show | 12 | HG00099.hp1 HG02723.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.432-4215dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94639037 | |||||
chr5:94639037
|
C | CTTTTT | 75 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(72): Show | 85 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.432-4219_432-4215d others(7): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94639037 | |||||
chr5:94639037
|
C | CTTTTTT | 9 | a0002c0002t0002g0246a0002c0002t0002g0291a0002c0002t0002g0294others(6): Show | 10 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.432-4220_432-4215d others(8): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94639037 | |||||
chr5:94639037
|
C | T | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.432-4236C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639037 | ||||||
chr5:94639037
|
CT | C | 46 | a0001c0001t0001g0139a0001c0001t0001g0210a0001c0001t0001g0323others(43): Show | 47 | HG00558.hp2 HG00741.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.432-4215delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr5 | 94639037 | |||||
chr5:94639091
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.432-4182A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639091 | ||||||
chr5:94639320
|
G | A | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-3953G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639320 | ||||||
chr5:94639345
|
A | C | 1 | a0001c0001t0003g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.432-3928A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639345 | ||||||
chr5:94639379
|
A | G | 1 | a0001c0001t0003g0116 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.432-3894A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639379 | ||||||
chr5:94639493
|
C | A | 1 | a0002c0002t0005g0305 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.432-3780C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639493 | ||||||
chr5:94639557
|
T | C | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.432-3716T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639557 | ||||||
chr5:94639607
|
T | C | 1 | a0002c0002t0002g0230 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.432-3666T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639607 | ||||||
chr5:94639637
|
A | G | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.432-3636A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639637 | ||||||
chr5:94639876
|
G | A | 1 | a0002c0002t0005g0300 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.432-3397G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639876 | ||||||
chr5:94639897
|
T | C | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.432-3376T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639897 | ||||||
chr5:94639907
|
G | C | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-3366G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94639907 | ||||||
chr5:94640015
|
G | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(98): Show | 104 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.432-3258G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640015 | ||||||
chr5:94640248
|
T | C | 219 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(216): Show | 233 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.432-3025T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640248 | ||||||
chr5:94640366
|
T | C | 1 | a0001c0001t0007g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.432-2907T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640366 | ||||||
chr5:94640370
|
G | A | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.432-2903G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640370 | ||||||
chr5:94640571
|
T | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-2702T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640571 | ||||||
chr5:94640611
|
T | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-2662T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640611 | ||||||
chr5:94640671
|
T | A | 93 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(90): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.432-2602T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640671 | ||||||
chr5:94640680
|
A | T | 1 | a0002c0002t0005g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.432-2593A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640680 | ||||||
chr5:94640694
|
T | C | 7 | a0001c0001t0007g0120a0001c0001t0007g0194a0001c0001t0007g0195others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.432-2579T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640694 | ||||||
chr5:94640817
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.432-2456C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640817 | ||||||
chr5:94640820
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0171a0001c0001t0001g0172others(1): Show | 5 | HG01071.hp1 HG01074.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.432-2453C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640820 | ||||||
chr5:94640838
|
T | C | 1 | a0001c0001t0001g0322 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.432-2435T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94640838 | ||||||
chr5:94641119
|
G | A | 1 | a0001c0001t0003g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.432-2154G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641119 | ||||||
chr5:94641159
|
A | G | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.432-2114A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641159 | ||||||
chr5:94641174
|
C | A | 1 | a0008c0014t0004g0032 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.432-2099C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641174 | ||||||
chr5:94641203
|
AACTCATG others(8): Show |
A | 1 | a0001c0001t0001g0322 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.432-2069_432-2055d others(17): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641203 | ||||||
chr5:94641332
|
CT | C | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.432-1940delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641332 | ||||||
chr5:94641354
|
A | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.432-1919A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641354 | ||||||
chr5:94641440
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.432-1833G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641440 | ||||||
chr5:94641458
|
G | A | 1 | a0001c0001t0004g0062 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.432-1815G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641458 | ||||||
chr5:94641458
|
G | T | 91 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(88): Show | 102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.432-1815G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641458 | ||||||
chr5:94641647
|
A | G | 1 | a0002c0002t0002g0238 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.432-1626A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641647 | ||||||
chr5:94641683
|
C | T | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.432-1590C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641683 | ||||||
chr5:94641995
|
C | T | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-1278C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94641995 | ||||||
chr5:94642036
|
T | G | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-1237T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94642036 | ||||||
chr5:94642213
|
C | T | 1 | a0002c0002t0005g0313 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.432-1060C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94642213 | ||||||
chr5:94642246
|
A | T | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.432-1027A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94642246 | ||||||
chr5:94642737
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.432-536G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94642737 | ||||||
chr5:94642769
|
A | G | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.432-504A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94642769 | ||||||
chr5:94642944
|
G | C | 1 | a0001c0001t0001g0152 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.432-329G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94642944 | ||||||
chr5:94643116
|
A | G | 2 | a0001c0003t0001g0162a0001c0003t0001g0179 | 2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.432-157A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94643116 | ||||||
chr5:94643244
|
A | C | 7 | a0001c0001t0007g0120a0001c0001t0007g0194a0001c0001t0007g0195others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.432-29A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94643244 | ||||||
chr5:94643246
|
T | A | 1 | a0001c0001t0001g0145 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.432-27T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 4/20 | chr5 | 94643246 | ||||||
chr5:94643510
|
T | C | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.594+75T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643510 | ||||||
chr5:94643519
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.594+84G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643519 | ||||||
chr5:94643642
|
T | G | 52 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(49): Show | 54 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.594+207T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643642 | ||||||
chr5:94643725
|
GGGGTTAT others(30): Show |
G | 1 | a0001c0001t0004g0017 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.594+296_594+332del others(37): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr5 | 94643725 | |||||
chr5:94643740
|
T | C | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.594+305T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643740 | ||||||
chr5:94643770
|
G | T | 1 | a0001c0001t0004g0017 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.594+335G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643770 | ||||||
chr5:94643772
|
A | C | 1 | a0001c0001t0004g0017 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.594+337A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643772 | ||||||
chr5:94643780
|
C | G | 1 | a0001c0001t0004g0017 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.594+345C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643780 | ||||||
chr5:94643781
|
C | A | 1 | a0001c0001t0004g0017 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.594+346C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643781 | ||||||
chr5:94643784
|
TCCTATTC others(3): Show |
T | 1 | a0001c0001t0004g0017 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.594+350_594+359del others(10): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643784 | ||||||
chr5:94643796
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.594+361A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643796 | ||||||
chr5:94643903
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.594+468C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94643903 | ||||||
chr5:94644036
|
C | T | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.594+601C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94644036 | ||||||
chr5:94644309
|
T | G | 110 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(107): Show | 113 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.594+874T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94644309 | ||||||
chr5:94644378
|
C | T | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.594+943C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94644378 | ||||||
chr5:94644481
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.594+1046A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94644481 | ||||||
chr5:94644531
|
C | T | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.594+1096C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94644531 | ||||||
chr5:94644644
|
C | A | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.594+1209C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94644644 | ||||||
chr5:94644849
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.594+1414G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94644849 | ||||||
chr5:94645018
|
G | A | 1 | a0001c0001t0004g0053 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.594+1583G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645018 | ||||||
chr5:94645065
|
A | G | 1 | a0002c0002t0005g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.594+1630A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645065 | ||||||
chr5:94645276
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.594+1841G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645276 | ||||||
chr5:94645405
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.594+1970G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645405 | ||||||
chr5:94645493
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0025g0192 | 2 | HG02723.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.594+2058G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645493 | ||||||
chr5:94645511
|
T | C | 1 | a0002c0002t0022g0312 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.594+2076T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645511 | ||||||
chr5:94645551
|
T | G | 3 | a0001c0001t0016g0193a0001c0001t0016g0289a0007c0013t0023g0269 | 3 | HG02055.hp1 HG03017.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.594+2116T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645551 | ||||||
chr5:94645559
|
G | T | 93 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(90): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.594+2124G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645559 | ||||||
chr5:94645728
|
T | C | 1 | a0002c0002t0002g0226 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.594+2293T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645728 | ||||||
chr5:94645734
|
G | A | 70 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(67): Show | 80 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.594+2299G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645734 | ||||||
chr5:94645799
|
A | T | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.594+2364A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645799 | ||||||
chr5:94645825
|
G | C | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.594+2390G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645825 | ||||||
chr5:94645890
|
A | G | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.594+2455A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645890 | ||||||
chr5:94645957
|
C | T | 4 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(1): Show | 4 | NA18940.hp2 NA18968.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+2522C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645957 | ||||||
chr5:94645982
|
G | A | 1 | a0001c0001t0007g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.594+2547G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94645982 | ||||||
chr5:94646013
|
A | G | 208 | a0001c0001t0002g0227a0001c0001t0003g0006a0001c0001t0003g0068others(205): Show | 222 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.594+2578A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94646013 | ||||||
chr5:94646249
|
C | T | 93 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(90): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.594+2814C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94646249 | ||||||
chr5:94646263
|
A | G | 1 | a0001c0001t0003g0084 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.594+2828A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94646263 | ||||||
chr5:94646278
|
A | T | 220 | a0001c0001t0002g0227a0001c0001t0003g0006a0001c0001t0003g0068others(217): Show | 234 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.594+2843A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94646278 | ||||||
chr5:94646635
|
T | C | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.595-2819T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94646635 | ||||||
chr5:94646662
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.595-2792A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94646662 | ||||||
chr5:94646868
|
C | T | 205 | a0001c0001t0002g0227a0001c0001t0003g0006a0001c0001t0003g0068others(202): Show | 219 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.595-2586C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94646868 | ||||||
chr5:94647083
|
A | G | 70 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(67): Show | 80 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.595-2371A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647083 | ||||||
chr5:94647322
|
T | C | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.595-2132T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647322 | ||||||
chr5:94647405
|
G | C | 218 | a0001c0001t0002g0227a0001c0001t0003g0006a0001c0001t0003g0068others(215): Show | 232 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.595-2049G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647405 | ||||||
chr5:94647508
|
T | G | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.595-1946T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647508 | ||||||
chr5:94647559
|
AG | A | 112 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(109): Show | 115 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.595-1894delG | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647559 | ||||||
chr5:94647656
|
A | T | 4 | a0002c0002t0002g0291a0002c0002t0002g0292a0002c0002t0002g0293others(1): Show | 4 | HG01167.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-1798A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647656 | ||||||
chr5:94647669
|
A | G | 2 | a0002c0002t0005g0307a0002c0002t0022g0312 | 2 | NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.595-1785A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647669 | ||||||
chr5:94647717
|
A | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01081.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.595-1737A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647717 | ||||||
chr5:94647726
|
A | G | 7 | a0001c0001t0004g0023a0001c0001t0004g0031a0001c0001t0004g0038others(4): Show | 7 | HG00558.hp1 NA18965.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.595-1728A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647726 | ||||||
chr5:94647767
|
A | AAT | 207 | a0001c0001t0002g0227a0001c0001t0003g0006a0001c0001t0003g0068others(204): Show | 221 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.595-1684_595-1683d others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr5 | 94647767 | |||||
chr5:94647772
|
G | A | 1 | a0001c0001t0004g0017 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.595-1682G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647772 | ||||||
chr5:94647907
|
C | A | 90 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(87): Show | 101 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.595-1547C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647907 | ||||||
chr5:94647938
|
A | C | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.595-1516A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647938 | ||||||
chr5:94647976
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.595-1478C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94647976 | ||||||
chr5:94648013
|
A | T | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.595-1441A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94648013 | ||||||
chr5:94648159
|
A | G | 211 | a0001c0001t0002g0227a0001c0001t0003g0006a0001c0001t0003g0068others(208): Show | 225 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.595-1295A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94648159 | ||||||
chr5:94648183
|
C | A | 2 | a0002c0002t0002g0247a0002c0002t0002g0288 | 2 | NA18953.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.595-1271C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94648183 | ||||||
chr5:94648322
|
T | A | 1 | a0002c0002t0002g0291 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.595-1132T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94648322 | ||||||
chr5:94648387
|
G | A | 93 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(90): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.595-1067G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94648387 | ||||||
chr5:94648523
|
C | G | 93 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(90): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.595-931C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94648523 | ||||||
chr5:94648700
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.595-754T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94648700 | ||||||
chr5:94648888
|
A | T | 1 | a0001c0001t0007g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.595-566A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94648888 | ||||||
chr5:94649004
|
A | T | 1 | a0001c0001t0003g0097 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.595-450A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94649004 | ||||||
chr5:94649047
|
C | G | 1 | a0003c0006t0001g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.595-407C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94649047 | ||||||
chr5:94649185
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.595-269A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 5/20 | chr5 | 94649185 | ||||||
chr5:94649602
|
A | G | 50 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(47): Show | 52 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(49): Show |
splice_region_variant&intron_variant | LOW | c.738+5A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94649602 | ||||||
chr5:94649739
|
T | C | 3 | a0002c0002t0002g0251a0002c0002t0002g0252a0002c0002t0002g0271 | 3 | HG02165.hp1 NA18960.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.738+142T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94649739 | ||||||
chr5:94649935
|
A | T | 2 | a0001c0005t0004g0283a0001c0005t0004g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.738+338A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94649935 | ||||||
chr5:94649950
|
T | C | 93 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(90): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.738+353T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94649950 | ||||||
chr5:94650115
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.738+518A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94650115 | ||||||
chr5:94650117
|
T | C | 90 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(87): Show | 101 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.738+520T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94650117 | ||||||
chr5:94650128
|
G | A | 90 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(87): Show | 101 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.738+531G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94650128 | ||||||
chr5:94650194
|
T | C | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.738+597T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94650194 | ||||||
chr5:94650284
|
A | G | 90 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(87): Show | 101 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.738+687A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94650284 | ||||||
chr5:94650316
|
A | G | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.738+719A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94650316 | ||||||
chr5:94650362
|
AT | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(219): Show | 228 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.738+783delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr5 | 94650362 | |||||
chr5:94650362
|
ATTT | A | 90 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(87): Show | 101 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.738+781_738+783del others(3): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr5 | 94650362 | |||||
chr5:94650422
|
G | A | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.738+825G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94650422 | ||||||
chr5:94650507
|
A | C | 90 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(87): Show | 101 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.738+910A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94650507 | ||||||
chr5:94650554
|
C | T | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.738+957C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94650554 | ||||||
chr5:94650818
|
C | T | 1 | a0005c0010t0001g0339 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.739-884C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94650818 | ||||||
chr5:94651103
|
A | G | 52 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(49): Show | 54 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.739-599A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651103 | ||||||
chr5:94651126
|
A | C | 1 | a0001c0001t0004g0064 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.739-576A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651126 | ||||||
chr5:94651165
|
A | C | 1 | a0002c0002t0005g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.739-537A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651165 | ||||||
chr5:94651256
|
C | T | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.739-446C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651256 | ||||||
chr5:94651405
|
T | C | 2 | a0001c0005t0004g0283a0001c0005t0004g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.739-297T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651405 | ||||||
chr5:94651485
|
A | G | 1 | a0001c0001t0025g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.739-217A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651485 | ||||||
chr5:94651496
|
C | T | 1 | a0001c0001t0003g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-206C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651496 | ||||||
chr5:94651502
|
A | G | 1 | a0002c0002t0002g0237 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.739-200A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651502 | ||||||
chr5:94651587
|
T | C | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.739-115T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651587 | ||||||
chr5:94651588
|
A | G | 8 | a0002c0002t0002g0272a0002c0002t0002g0273a0002c0002t0002g0274others(5): Show | 8 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.739-114A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651588 | ||||||
chr5:94651609
|
C | A | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.739-93C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 6/20 | chr5 | 94651609 | ||||||
chr5:94651849
|
C | T | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
splice_region_variant&intron_variant | LOW | c.882+4C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94651849 | ||||||
chr5:94651951
|
A | G | 50 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(47): Show | 52 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.882+106A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94651951 | ||||||
chr5:94651992
|
C | T | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.882+147C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94651992 | ||||||
chr5:94652007
|
C | CTTTTTTC others(2): Show |
23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.882+169_882+177dup others(9): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 94652007 | |||||
chr5:94652014
|
CT | C | 113 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(110): Show | 116 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.882+181delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 94652014 | |||||
chr5:94652015
|
T | TTTTTTTT others(1): Show |
70 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(67): Show | 80 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.882+177_882+178ins others(8): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 94652015 | |||||
chr5:94652239
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.882+394G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94652239 | ||||||
chr5:94652263
|
C | A | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.882+418C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94652263 | ||||||
chr5:94652269
|
A | T | 1 | a0001c0001t0006g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882+424A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94652269 | ||||||
chr5:94652349
|
C | T | 93 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(90): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.882+504C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94652349 | ||||||
chr5:94652497
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | NA18940.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.882+652T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94652497 | ||||||
chr5:94652711
|
G | A | 1 | a0002c0002t0005g0300 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.883-561G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94652711 | ||||||
chr5:94652718
|
C | T | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-554C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94652718 | ||||||
chr5:94652780
|
G | A | 93 | a0001c0001t0002g0227a0002c0002t0002g0002a0002c0002t0002g0003others(90): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.883-492G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94652780 | ||||||
chr5:94652943
|
C | T | 2 | a0001c0001t0003g0070a0001c0001t0003g0088 | 2 | HG00741.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.883-329C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94652943 | ||||||
chr5:94653015
|
G | A | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.883-257G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94653015 | ||||||
chr5:94653083
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.883-189C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94653083 | ||||||
chr5:94653104
|
G | A | 1 | a0001c0009t0003g0113 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.883-168G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94653104 | ||||||
chr5:94653122
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.883-150G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94653122 | ||||||
chr5:94653169
|
T | C | 5 | a0002c0002t0002g0008a0002c0002t0002g0229a0002c0002t0002g0230others(2): Show | 6 | HG02155.hp2 NA18968.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-103T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94653169 | ||||||
chr5:94653187
|
G | A | 1 | a0002c0002t0005g0313 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.883-85G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 7/20 | chr5 | 94653187 | ||||||
chr5:94653432
|
T | C | 3 | a0001c0001t0003g0006a0001c0001t0003g0082a0001c0001t0003g0083 | 4 | HG01243.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032+11T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | chr5 | 94653432 | ||||||
chr5:94653484
|
C | T | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1032+63C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | chr5 | 94653484 | ||||||
chr5:94653530
|
C | A | 2 | a0002c0002t0002g0251a0002c0002t0002g0271 | 2 | HG02165.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1032+109C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | chr5 | 94653530 | ||||||
chr5:94653544
|
A | G | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1032+123A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | chr5 | 94653544 | ||||||
chr5:94653823
|
GCTT | G | 3 | a0001c0001t0001g0335a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01975.hp2 HG02293.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1032+406_1032+408d others(5): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 94653823 | |||||
chr5:94653841
|
T | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1032+420T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | chr5 | 94653841 | ||||||
chr5:94653854
|
CT | C | 208 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(205): Show | 222 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1032+446delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 94653854 | |||||
chr5:94653871
|
G | C | 1 | a0001c0001t0025g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1032+450G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | chr5 | 94653871 | ||||||
chr5:94653894
|
G | C | 1 | a0001c0001t0007g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1032+473G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | chr5 | 94653894 | ||||||
chr5:94653962
|
C | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1032+541C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | chr5 | 94653962 | ||||||
chr5:94654031
|
A | G | 54 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(51): Show | 56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1033-599A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | chr5 | 94654031 | ||||||
chr5:94654394
|
G | GA | 64 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(61): Show | 74 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1033-221dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 94654394 | |||||
chr5:94654394
|
GA | G | 27 | a0001c0001t0001g0161a0001c0001t0007g0120a0001c0001t0007g0194others(24): Show | 28 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.1033-221delA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 94654394 | |||||
chr5:94654455
|
G | A | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1033-175G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 8/20 | chr5 | 94654455 | ||||||
chr5:94654766
|
C | T | 1 | a0001c0001t0012g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1155+14C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94654766 | ||||||
chr5:94654958
|
A | G | 58 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(55): Show | 68 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1155+206A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94654958 | ||||||
chr5:94655031
|
T | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1155+279T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655031 | ||||||
chr5:94655202
|
C | T | 212 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(209): Show | 226 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1155+450C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655202 | ||||||
chr5:94655257
|
A | G | 1 | a0002c0002t0022g0312 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1155+505A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655257 | ||||||
chr5:94655356
|
A | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1155+604A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655356 | ||||||
chr5:94655533
|
C | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1155+781C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655533 | ||||||
chr5:94655572
|
T | G | 1 | a0001c0001t0004g0040 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1155+820T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655572 | ||||||
chr5:94655614
|
G | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1155+862G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655614 | ||||||
chr5:94655769
|
A | C | 1 | a0001c0001t0003g0091 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1155+1017A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655769 | ||||||
chr5:94655799
|
T | C | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1155+1047T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655799 | ||||||
chr5:94655872
|
A | G | 7 | a0001c0001t0007g0120a0001c0001t0007g0194a0001c0001t0007g0195others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155+1120A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655872 | ||||||
chr5:94655884
|
A | G | 1 | a0001c0001t0001g0327 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1155+1132A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655884 | ||||||
chr5:94655888
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1155+1136C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94655888 | ||||||
chr5:94656027
|
A | C | 1 | a0001c0004t0004g0024 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1155+1275A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656027 | ||||||
chr5:94656077
|
A | G | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1155+1325A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656077 | ||||||
chr5:94656114
|
A | G | 1 | a0001c0001t0001g0206 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1155+1362A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656114 | ||||||
chr5:94656114
|
A | T | 2 | a0001c0005t0004g0283a0001c0005t0004g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1155+1362A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656114 | ||||||
chr5:94656291
|
T | C | 4 | a0002c0002t0002g0008a0002c0002t0002g0229a0002c0002t0002g0230others(1): Show | 5 | HG02155.hp2 NA18970.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1155+1539T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656291 | ||||||
chr5:94656292
|
GTACACTT others(39): Show |
G | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1155+1560_1155+160 others(50): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94656292 | |||||
chr5:94656357
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1155+1605A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656357 | ||||||
chr5:94656363
|
T | C | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1155+1611T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656363 | ||||||
chr5:94656364
|
C | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1155+1612C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656364 | ||||||
chr5:94656526
|
C | T | 1 | a0001c0001t0007g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1155+1774C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656526 | ||||||
chr5:94656634
|
T | C | 1 | a0001c0001t0007g0120 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1155+1882T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656634 | ||||||
chr5:94656648
|
T | A | 3 | a0002c0002t0002g0292a0002c0002t0002g0293a0002c0002t0002g0294 | 3 | HG01167.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1155+1896T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656648 | ||||||
chr5:94656841
|
TTTTA | T | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.1155+2097_1155+210 others(8): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94656841 | |||||
chr5:94656916
|
A | T | 1 | a0001c0001t0025g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1155+2164A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656916 | ||||||
chr5:94656947
|
T | C | 221 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(218): Show | 235 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1155+2195T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656947 | ||||||
chr5:94656949
|
A | G | 2 | a0001c0005t0004g0283a0001c0005t0004g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1155+2197A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94656949 | ||||||
chr5:94657014
|
T | A | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1155+2262T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657014 | ||||||
chr5:94657046
|
T | C | 2 | a0001c0005t0004g0283a0001c0005t0004g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1155+2294T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657046 | ||||||
chr5:94657074
|
C | G | 1 | a0001c0001t0006g0185 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1155+2322C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657074 | ||||||
chr5:94657097
|
T | A | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1155+2345T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657097 | ||||||
chr5:94657196
|
C | G | 31 | a0001c0001t0003g0070a0001c0001t0003g0071a0001c0001t0003g0072others(28): Show | 31 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.1155+2444C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657196 | ||||||
chr5:94657310
|
G | A | 31 | a0001c0001t0003g0070a0001c0001t0003g0071a0001c0001t0003g0072others(28): Show | 31 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.1155+2558G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657310 | ||||||
chr5:94657421
|
C | A | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1155+2669C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657421 | ||||||
chr5:94657439
|
T | G | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.1155+2687T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657439 | ||||||
chr5:94657470
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1155+2718C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657470 | ||||||
chr5:94657648
|
C | T | 1 | a0001c0004t0004g0060 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1155+2896C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657648 | ||||||
chr5:94657717
|
C | T | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1155+2965C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657717 | ||||||
chr5:94657740
|
T | C | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1155+2988T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657740 | ||||||
chr5:94657770
|
G | A | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1155+3018G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657770 | ||||||
chr5:94657931
|
A | G | 2 | a0002c0002t0002g0008a0002c0002t0002g0231 | 3 | NA18970.hp1 NA18975.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1155+3179A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94657931 | ||||||
chr5:94658139
|
G | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1155+3387G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94658139 | ||||||
chr5:94658162
|
G | GT | 39 | a0001c0001t0015g0281a0001c0001t0015g0282a0002c0002t0002g0224others(36): Show | 40 | HG00140.hp2 HG01099.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.1155+3423dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94658162 | |||||
chr5:94658162
|
G | GTT | 54 | a0001c0001t0002g0255a0002c0002t0002g0002a0002c0002t0002g0003others(51): Show | 64 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1155+3422_1155+342 others(6): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94658162 | |||||
chr5:94658196
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1155+3444C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94658196 | ||||||
chr5:94658270
|
G | A | 1 | a0001c0001t0003g0097 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1155+3518G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94658270 | ||||||
chr5:94658391
|
G | T | 56 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(53): Show | 57 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.1155+3639G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94658391 | ||||||
chr5:94658402
|
A | G | 1 | a0001c0001t0004g0030 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1155+3650A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94658402 | ||||||
chr5:94658428
|
T | TTTG | 59 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(56): Show | 60 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(57): Show |
intron_variant | MODIFIER | c.1155+3703_1155+370 others(7): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94658428 | |||||
chr5:94658428
|
T | TTTGTTG | 70 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(67): Show | 80 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.1155+3700_1155+370 others(10): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94658428 | |||||
chr5:94658428
|
TTTG | T | 22 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(19): Show | 23 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.1155+3703_1155+370 others(7): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94658428 | |||||
chr5:94658514
|
C | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1155+3762C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94658514 | ||||||
chr5:94658576
|
T | C | 3 | a0002c0002t0002g0273a0002c0002t0002g0274a0002c0002t0002g0275 | 3 | HG06807.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1156-3722T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94658576 | ||||||
chr5:94658700
|
A | G | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.1156-3598A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94658700 | ||||||
chr5:94658811
|
CT | C | 93 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(90): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1156-3479delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94658811 | |||||
chr5:94658821
|
G | A | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1156-3477G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94658821 | ||||||
chr5:94658832
|
TATTTCAA others(107): Show |
T | 17 | a0001c0008t0006g0157a0002c0002t0002g0235a0002c0002t0002g0241others(14): Show | 18 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1156-3232_1156-311 others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94658832 | |||||
chr5:94658913
|
T | C | 1 | a0001c0001t0001g0007 | 2 | HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1156-3385T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94658913 | ||||||
chr5:94659196
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0214others(1): Show | 4 | NA18979.hp2 NA18981.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-3102A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94659196 | ||||||
chr5:94659363
|
GAGAATTA others(4): Show |
G | 1 | a0001c0001t0007g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1156-2934_1156-292 others(15): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94659363 | ||||||
chr5:94659375
|
G | T | 1 | a0001c0001t0007g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1156-2923G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94659375 | ||||||
chr5:94659433
|
C | T | 2 | a0002c0002t0005g0119a0002c0002t0005g0297 | 2 | NA18972.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1156-2865C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94659433 | ||||||
chr5:94659475
|
A | T | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.1156-2823A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94659475 | ||||||
chr5:94659611
|
T | G | 4 | a0001c0001t0001g0319a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | NA18984.hp2 NA19010.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-2687T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94659611 | ||||||
chr5:94659884
|
A | G | 221 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(218): Show | 235 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1156-2414A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94659884 | ||||||
chr5:94659920
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1156-2378G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94659920 | ||||||
chr5:94659960
|
A | T | 1 | a0001c0001t0005g0073 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1156-2338A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94659960 | ||||||
chr5:94660357
|
T | A | 1 | a0001c0003t0001g0167 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1156-1941T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94660357 | ||||||
chr5:94660411
|
C | T | 1 | a0002c0002t0005g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1156-1887C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94660411 | ||||||
chr5:94660469
|
C | T | 1 | a0001c0001t0025g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1156-1829C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94660469 | ||||||
chr5:94660477
|
T | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1156-1821T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94660477 | ||||||
chr5:94660571
|
C | T | 58 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(55): Show | 68 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1156-1727C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94660571 | ||||||
chr5:94660694
|
C | T | 5 | a0001c0001t0003g0075a0001c0001t0003g0102a0001c0001t0003g0104others(2): Show | 5 | HG01358.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1156-1604C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94660694 | ||||||
chr5:94660917
|
G | A | 52 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(49): Show | 54 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1156-1381G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94660917 | ||||||
chr5:94660966
|
C | A | 2 | a0002c0002t0002g0251a0002c0002t0002g0271 | 2 | HG02165.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1156-1332C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94660966 | ||||||
chr5:94661034
|
G | A | 4 | a0001c0001t0001g0334a0001c0001t0001g0338a0001c0001t0001g0341others(1): Show | 4 | HG00423.hp1 HG03704.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-1264G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94661034 | ||||||
chr5:94661058
|
T | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1156-1240T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94661058 | ||||||
chr5:94661181
|
A | G | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1156-1117A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94661181 | ||||||
chr5:94661382
|
C | A | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1156-916C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94661382 | ||||||
chr5:94661539
|
G | GT | 6 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0015g0281others(3): Show | 6 | HG02723.hp1 HG02818.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1156-746dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94661539 | |||||
chr5:94661545
|
T | A | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1156-753T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94661545 | ||||||
chr5:94661639
|
A | G | 67 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(64): Show | 77 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1156-659A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94661639 | ||||||
chr5:94661670
|
A | G | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1156-628A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94661670 | ||||||
chr5:94661694
|
G | A | 49 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(46): Show | 51 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1156-604G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94661694 | ||||||
chr5:94661749
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1156-549C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94661749 | ||||||
chr5:94662153
|
TTGAGTAA others(9): Show |
T | 1 | a0002c0002t0002g0253 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1156-143_1156-128d others(18): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94662153 | |||||
chr5:94662171
|
C | T | 1 | a0002c0002t0002g0253 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1156-127C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94662171 | ||||||
chr5:94662181
|
A | G | 1 | a0002c0002t0005g0307 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1156-117A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94662181 | ||||||
chr5:94662207
|
G | GTTTTATA others(4): Show |
1 | a0002c0002t0002g0253 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1156-87_1156-77dup others(11): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 94662207 | |||||
chr5:94662282
|
G | C | 1 | a0001c0001t0003g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1156-16G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 9/20 | chr5 | 94662282 | ||||||
chr5:94662407
|
G | GTTA | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1209+60_1209+62dup others(3): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr5 | 94662407 | |||||
chr5:94662493
|
C | A | 12 | a0001c0001t0001g0021a0001c0001t0001g0200a0001c0001t0001g0204others(9): Show | 12 | HG00558.hp2 HG02015.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.1209+142C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94662493 | ||||||
chr5:94662498
|
A | G | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1209+147A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94662498 | ||||||
chr5:94662515
|
T | C | 2 | a0001c0001t0004g0033a0001c0001t0004g0034 | 2 | NA18950.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1209+164T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94662515 | ||||||
chr5:94662673
|
G | A | 345 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0020others(342): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1209+322G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94662673 | ||||||
chr5:94662751
|
T | TAAAC | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1209+401_1209+404d others(6): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr5 | 94662751 | |||||
chr5:94662801
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0317 | 2 | NA18943.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1209+450G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94662801 | ||||||
chr5:94663119
|
C | G | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1210-631C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94663119 | ||||||
chr5:94663135
|
C | G | 1 | a0002c0002t0022g0312 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1210-615C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94663135 | ||||||
chr5:94663197
|
A | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1210-553A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94663197 | ||||||
chr5:94663296
|
C | G | 1 | a0002c0002t0002g0235 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1210-454C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94663296 | ||||||
chr5:94663377
|
C | T | 2 | a0001c0004t0004g0024a0001c0004t0004g0060 | 2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1210-373C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94663377 | ||||||
chr5:94663400
|
T | C | 1 | a0001c0001t0003g0092 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1210-350T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94663400 | ||||||
chr5:94663475
|
C | A | 1 | a0001c0001t0025g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1210-275C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94663475 | ||||||
chr5:94663481
|
T | G | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1210-269T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94663481 | ||||||
chr5:94663498
|
G | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0290 | 2 | HG03239.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1210-252G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94663498 | ||||||
chr5:94663726
|
A | C | 52 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(49): Show | 54 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1210-24A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 10/20 | chr5 | 94663726 | ||||||
chr5:94663936
|
C | T | 1 | a0001c0001t0004g0022 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1368+28C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94663936 | ||||||
chr5:94664132
|
T | A | 2 | a0002c0002t0005g0296a0002c0002t0005g0315 | 2 | NA19011.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1368+224T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94664132 | ||||||
chr5:94664334
|
G | A | 1 | a0001c0001t0004g0063 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1368+426G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94664334 | ||||||
chr5:94664401
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1368+493C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94664401 | ||||||
chr5:94664501
|
C | T | 1 | a0001c0001t0003g0112 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1368+593C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94664501 | ||||||
chr5:94664559
|
G | A | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1368+651G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94664559 | ||||||
chr5:94664601
|
A | G | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1368+693A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94664601 | ||||||
chr5:94664655
|
G | T | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1368+747G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94664655 | ||||||
chr5:94664656
|
C | T | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1368+748C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94664656 | ||||||
chr5:94664672
|
CT | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1368+768delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 94664672 | |||||
chr5:94665066
|
A | G | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1369-795A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665066 | ||||||
chr5:94665067
|
G | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1369-794G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665067 | ||||||
chr5:94665170
|
G | A | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1369-691G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665170 | ||||||
chr5:94665250
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | NA18984.hp2 NA19010.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1369-611A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665250 | ||||||
chr5:94665413
|
A | T | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1369-448A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665413 | ||||||
chr5:94665453
|
A | G | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1369-408A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665453 | ||||||
chr5:94665469
|
G | T | 113 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(110): Show | 116 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.1369-392G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665469 | ||||||
chr5:94665547
|
A | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1369-314A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665547 | ||||||
chr5:94665582
|
C | G | 1 | a0001c0001t0007g0194 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1369-279C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665582 | ||||||
chr5:94665638
|
A | G | 1 | a0001c0001t0003g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1369-223A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665638 | ||||||
chr5:94665688
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1369-173G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665688 | ||||||
chr5:94665747
|
C | G | 1 | a0001c0001t0025g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1369-114C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665747 | ||||||
chr5:94665771
|
A | G | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.1369-90A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665771 | ||||||
chr5:94665804
|
G | A | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1369-57G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 11/20 | chr5 | 94665804 | ||||||
chr5:94666178
|
A | G | 1 | a0001c0001t0003g0077 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1532+154A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94666178 | ||||||
chr5:94666343
|
A | G | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1532+319A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94666343 | ||||||
chr5:94666577
|
G | T | 2 | a0002c0002t0002g0008a0002c0002t0002g0231 | 3 | NA18970.hp1 NA18975.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1532+553G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94666577 | ||||||
chr5:94666594
|
G | C | 113 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(110): Show | 116 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.1532+570G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94666594 | ||||||
chr5:94666671
|
C | T | 2 | a0002c0002t0002g0223a0002c0002t0002g0259 | 2 | HG00735.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1532+647C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94666671 | ||||||
chr5:94666865
|
G | A | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1532+841G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94666865 | ||||||
chr5:94666953
|
C | CT | 65 | a0001c0001t0001g0155a0001c0001t0001g0184a0001c0001t0001g0334others(62): Show | 67 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1532+952dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr5 | 94666953 | |||||
chr5:94666953
|
C | CTT | 64 | a0001c0001t0001g0341a0001c0001t0002g0255a0002c0002t0002g0002others(61): Show | 74 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1532+951_1532+952d others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr5 | 94666953 | |||||
chr5:94666953
|
C | CTTT | 20 | a0001c0001t0002g0227a0002c0002t0002g0268a0002c0002t0005g0013others(17): Show | 21 | HG00140.hp2 HG01346.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1532+950_1532+952d others(5): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr5 | 94666953 | |||||
chr5:94666953
|
CT | C | 57 | a0001c0001t0001g0344a0001c0001t0003g0006a0001c0001t0003g0070others(54): Show | 58 | HG00741.hp1 HG01074.hp1 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.1532+952delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr5 | 94666953 | |||||
chr5:94667016
|
A | G | 5 | a0001c0001t0007g0120a0001c0001t0007g0196a0001c0001t0007g0197others(2): Show | 5 | HG02258.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1532+992A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94667016 | ||||||
chr5:94667497
|
C | T | 2 | a0001c0001t0003g0077a0001c0001t0003g0078 | 2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1532+1473C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94667497 | ||||||
chr5:94667578
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1532+1554A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94667578 | ||||||
chr5:94667591
|
G | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1532+1567G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94667591 | ||||||
chr5:94667608
|
C | T | 1 | a0002c0002t0022g0312 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1532+1584C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94667608 | ||||||
chr5:94667744
|
T | G | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+1720T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94667744 | ||||||
chr5:94667749
|
G | A | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1532+1725G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94667749 | ||||||
chr5:94667860
|
C | T | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1532+1836C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94667860 | ||||||
chr5:94667861
|
G | A | 52 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(49): Show | 54 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1532+1837G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94667861 | ||||||
chr5:94667946
|
C | G | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1532+1922C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94667946 | ||||||
chr5:94668044
|
C | G | 209 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(206): Show | 223 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1532+2020C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94668044 | ||||||
chr5:94668053
|
G | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1532+2029G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94668053 | ||||||
chr5:94668254
|
C | T | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1533-1897C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94668254 | ||||||
chr5:94668316
|
T | C | 52 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(49): Show | 54 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-1835T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94668316 | ||||||
chr5:94668412
|
C | T | 3 | a0002c0002t0002g0292a0002c0002t0002g0293a0002c0002t0002g0294 | 3 | HG01167.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1533-1739C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94668412 | ||||||
chr5:94668419
|
C | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1533-1732C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94668419 | ||||||
chr5:94668583
|
G | A | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1533-1568G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94668583 | ||||||
chr5:94668877
|
A | G | 1 | a0001c0001t0006g0168 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1533-1274A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94668877 | ||||||
chr5:94668884
|
C | T | 54 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(51): Show | 56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1533-1267C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94668884 | ||||||
chr5:94668923
|
G | A | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.1533-1228G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94668923 | ||||||
chr5:94669135
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1533-1016G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94669135 | ||||||
chr5:94669200
|
G | A | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1533-951G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94669200 | ||||||
chr5:94669203
|
A | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1533-948A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94669203 | ||||||
chr5:94669245
|
T | C | 1 | a0001c0001t0007g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1533-906T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94669245 | ||||||
chr5:94669255
|
A | G | 1 | a0001c0001t0004g0064 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1533-896A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94669255 | ||||||
chr5:94669269
|
T | C | 212 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(209): Show | 226 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1533-882T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94669269 | ||||||
chr5:94669288
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1533-863A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94669288 | ||||||
chr5:94669395
|
T | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1533-756T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94669395 | ||||||
chr5:94669473
|
A | G | 3 | a0001c0001t0001g0327a0001c0001t0001g0329a0001c0001t0019g0270 | 3 | HG03942.hp2 HG04204.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1533-678A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94669473 | ||||||
chr5:94669595
|
GC | G | 3 | a0001c0001t0004g0044a0001c0001t0004g0045a0001c0001t0004g0053 | 3 | NA18946.hp1 NA18967.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1533-554delC | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr5 | 94669595 | |||||
chr5:94669677
|
A | C | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1533-474A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | chr5 | 94669677 | ||||||
chr5:94669704
|
T | TA | 157 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0004g0004others(154): Show | 170 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1533-441dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr5 | 94669704 | |||||
chr5:94669704
|
T | TAA | 55 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(52): Show | 56 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.1533-442_1533-441d others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr5 | 94669704 | |||||
chr5:94670293
|
G | A | 1 | a0001c0001t0015g0282 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1661+14G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 13/20 | chr5 | 94670293 | ||||||
chr5:94670318
|
T | C | 212 | a0001c0001t0001g0146a0001c0001t0002g0227a0001c0001t0002g0255others(209): Show | 226 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1661+39T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 13/20 | chr5 | 94670318 | ||||||
chr5:94670555
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1661+276A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 13/20 | chr5 | 94670555 | ||||||
chr5:94670741
|
A | G | 1 | a0001c0001t0004g0016 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1662-102A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 13/20 | chr5 | 94670741 | ||||||
chr5:94671089
|
T | C | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1827+81T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94671089 | ||||||
chr5:94671097
|
A | T | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1827+89A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94671097 | ||||||
chr5:94671148
|
T | TTATC | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1827+142_1827+143i others(6): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94671148 | |||||
chr5:94671366
|
T | C | 2 | a0001c0001t0007g0194a0001c0001t0007g0195 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1827+358T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94671366 | ||||||
chr5:94671396
|
C | T | 1 | a0002c0002t0002g0226 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1827+388C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94671396 | ||||||
chr5:94671409
|
TGA | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0172 | 3 | HG01071.hp1 HG01074.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1827+403_1827+404d others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94671409 | |||||
chr5:94671536
|
ATTTTGGT others(22): Show |
A | 1 | a0002c0002t0002g0288 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1827+533_1827+561d others(31): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94671536 | |||||
chr5:94671616
|
T | G | 9 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(6): Show | 10 | HG01243.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1827+608T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94671616 | ||||||
chr5:94671650
|
A | AT | 10 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(7): Show | 10 | HG00741.hp2 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1827+657dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94671650 | |||||
chr5:94671924
|
G | A | 1 | a0001c0001t0004g0017 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1827+916G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94671924 | ||||||
chr5:94672016
|
A | G | 1 | a0002c0002t0005g0306 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1827+1008A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94672016 | ||||||
chr5:94672118
|
A | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1827+1110A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94672118 | ||||||
chr5:94672119
|
T | C | 3 | a0002c0002t0002g0292a0002c0002t0002g0293a0002c0002t0002g0294 | 3 | HG01167.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1827+1111T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94672119 | ||||||
chr5:94672315
|
A | G | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1827+1307A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94672315 | ||||||
chr5:94672387
|
C | T | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1827+1379C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94672387 | ||||||
chr5:94672473
|
C | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0333 | 2 | NA18966.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1827+1465C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94672473 | ||||||
chr5:94672535
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1827+1527A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94672535 | ||||||
chr5:94672562
|
G | A | 332 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0020others(329): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.1827+1554G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94672562 | ||||||
chr5:94672807
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0317 | 2 | NA18943.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1827+1799T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94672807 | ||||||
chr5:94672955
|
T | G | 1 | a0001c0001t0001g0329 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1827+1947T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94672955 | ||||||
chr5:94673102
|
C | T | 7 | a0001c0001t0007g0120a0001c0001t0007g0194a0001c0001t0007g0195others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1827+2094C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94673102 | ||||||
chr5:94673141
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1827+2133C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94673141 | ||||||
chr5:94673153
|
T | C | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.1827+2145T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94673153 | ||||||
chr5:94673161
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1827+2153A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94673161 | ||||||
chr5:94673264
|
C | A | 221 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(218): Show | 235 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1827+2256C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94673264 | ||||||
chr5:94673413
|
G | A | 3 | a0001c0001t0001g0335a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01975.hp2 HG02293.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1827+2405G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94673413 | ||||||
chr5:94673691
|
T | TA | 8 | a0001c0001t0001g0121a0001c0001t0001g0204a0001c0001t0001g0214others(5): Show | 8 | HG00423.hp1 HG01175.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1827+2707dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94673691 | |||||
chr5:94673691
|
TA | T | 118 | a0001c0001t0001g0149a0001c0001t0001g0207a0001c0001t0001g0335others(115): Show | 121 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.1827+2707delA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94673691 | |||||
chr5:94673691
|
TAA | T | 65 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0086others(62): Show | 75 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1827+2706_1827+270 others(6): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94673691 | |||||
chr5:94673691
|
TAAAAAAA others(5): Show |
T | 1 | a0002c0002t0002g0225 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1827+2696_1827+270 others(16): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94673691 | |||||
chr5:94673713
|
AAAT | A | 18 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(15): Show | 19 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1827+2706_1827+270 others(7): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94673713 | ||||||
chr5:94673841
|
T | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(29): Show | 35 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1827+2833T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94673841 | ||||||
chr5:94673925
|
A | T | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1827+2917A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94673925 | ||||||
chr5:94673951
|
G | A | 70 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(67): Show | 80 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.1827+2943G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94673951 | ||||||
chr5:94674636
|
A | G | 1 | a0001c0001t0004g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1827+3628A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94674636 | ||||||
chr5:94674926
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1828-3882T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94674926 | ||||||
chr5:94675539
|
A | G | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1828-3269A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94675539 | ||||||
chr5:94675634
|
T | A | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1828-3174T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94675634 | ||||||
chr5:94675656
|
A | G | 1 | a0002c0002t0002g0261 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1828-3152A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94675656 | ||||||
chr5:94675904
|
A | AT | 150 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(147): Show | 155 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1828-2882dupT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94675904 | |||||
chr5:94675904
|
A | ATT | 26 | a0001c0001t0001g0139a0001c0001t0001g0216a0001c0001t0003g0081others(23): Show | 27 | HG00140.hp2 HG01099.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1828-2883_1828-288 others(6): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94675904 | |||||
chr5:94675904
|
AT | A | 12 | a0001c0001t0001g0322a0001c0001t0001g0336a0001c0001t0003g0077others(9): Show | 12 | HG01167.hp2 HG01261.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1828-2882delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94675904 | |||||
chr5:94676087
|
C | T | 2 | a0001c0001t0003g0117a0001c0001t0003g0118 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1828-2721C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94676087 | ||||||
chr5:94676089
|
A | G | 6 | a0001c0001t0004g0035a0001c0001t0004g0040a0001c0001t0004g0041others(3): Show | 6 | HG02027.hp2 HG02071.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1828-2719A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94676089 | ||||||
chr5:94676264
|
G | A | 1 | a0002c0002t0002g0249 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1828-2544G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94676264 | ||||||
chr5:94676275
|
C | A | 2 | a0001c0005t0004g0283a0001c0005t0004g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1828-2533C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94676275 | ||||||
chr5:94676336
|
G | T | 1 | a0002c0002t0002g0235 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1828-2472G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94676336 | ||||||
chr5:94676337
|
C | T | 1 | a0002c0002t0002g0235 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1828-2471C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94676337 | ||||||
chr5:94676557
|
G | A | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1828-2251G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94676557 | ||||||
chr5:94677049
|
C | A | 1 | a0002c0002t0002g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1828-1759C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677049 | ||||||
chr5:94677162
|
C | A | 1 | a0001c0001t0001g0205 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1828-1646C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677162 | ||||||
chr5:94677210
|
A | C | 1 | a0002c0002t0005g0297 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1828-1598A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677210 | ||||||
chr5:94677266
|
A | G | 1 | a0001c0011t0006g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1828-1542A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677266 | ||||||
chr5:94677273
|
C | T | 29 | a0001c0001t0001g0153a0001c0001t0001g0316a0001c0001t0001g0317others(26): Show | 29 | HG00423.hp1 HG01071.hp2 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.1828-1535C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677273 | ||||||
chr5:94677274
|
G | A | 212 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(209): Show | 226 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1828-1534G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677274 | ||||||
chr5:94677311
|
G | A | 1 | a0002c0002t0005g0315 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1828-1497G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677311 | ||||||
chr5:94677373
|
G | A | 3 | a0001c0001t0003g0072a0001c0001t0003g0100a0001c0001t0003g0106 | 3 | HG01257.hp2 HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1828-1435G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677373 | ||||||
chr5:94677454
|
T | C | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1828-1354T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677454 | ||||||
chr5:94677536
|
T | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1828-1272T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677536 | ||||||
chr5:94677731
|
A | C | 1 | a0002c0002t0005g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1828-1077A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677731 | ||||||
chr5:94677840
|
G | A | 1 | a0002c0002t0002g0221 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1828-968G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94677840 | ||||||
chr5:94677924
|
CT | C | 162 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(159): Show | 174 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1828-870delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 94677924 | |||||
chr5:94678070
|
G | A | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1828-738G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94678070 | ||||||
chr5:94678122
|
G | A | 67 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(64): Show | 77 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1828-686G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94678122 | ||||||
chr5:94678177
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1828-631C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94678177 | ||||||
chr5:94678515
|
G | A | 1 | a0002c0002t0002g0291 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1828-293G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94678515 | ||||||
chr5:94678788
|
T | A | 1 | a0001c0001t0001g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1828-20T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 14/20 | chr5 | 94678788 | ||||||
chr5:94678990
|
A | G | 1 | a0002c0002t0013g0264 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1975+35A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94678990 | ||||||
chr5:94679095
|
T | A | 212 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(209): Show | 226 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1975+140T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679095 | ||||||
chr5:94679264
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1975+309A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679264 | ||||||
chr5:94679292
|
A | T | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1975+337A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679292 | ||||||
chr5:94679306
|
A | G | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1975+351A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679306 | ||||||
chr5:94679359
|
C | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1975+404C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679359 | ||||||
chr5:94679422
|
T | C | 1 | a0001c0001t0003g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1975+467T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679422 | ||||||
chr5:94679428
|
TA | T | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1975+482delA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr5 | 94679428 | |||||
chr5:94679437
|
AT | A | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1975+485delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr5 | 94679437 | |||||
chr5:94679602
|
A | C | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1975+647A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679602 | ||||||
chr5:94679605
|
A | C | 1 | a0001c0001t0006g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1975+650A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679605 | ||||||
chr5:94679640
|
A | T | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1975+685A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679640 | ||||||
chr5:94679795
|
T | C | 1 | a0002c0002t0002g0257 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1975+840T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679795 | ||||||
chr5:94679835
|
T | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1975+880T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94679835 | ||||||
chr5:94680031
|
T | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1975+1076T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94680031 | ||||||
chr5:94680420
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1975+1465C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94680420 | ||||||
chr5:94680549
|
T | G | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1975+1594T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94680549 | ||||||
chr5:94680582
|
G | A | 67 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(64): Show | 77 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1975+1627G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94680582 | ||||||
chr5:94680623
|
T | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0146 | 2 | HG02132.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1975+1668T>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94680623 | ||||||
chr5:94680841
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1975+1886A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94680841 | ||||||
chr5:94681065
|
G | T | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1975+2110G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94681065 | ||||||
chr5:94681156
|
G | T | 1 | a0001c0011t0006g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1975+2201G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94681156 | ||||||
chr5:94681198
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1975+2243C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94681198 | ||||||
chr5:94681228
|
C | T | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1975+2273C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94681228 | ||||||
chr5:94681367
|
G | A | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1975+2412G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94681367 | ||||||
chr5:94681383
|
C | T | 2 | a0001c0001t0012g0189a0001c0001t0012g0190 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1975+2428C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94681383 | ||||||
chr5:94681446
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1975+2491G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94681446 | ||||||
chr5:94681830
|
T | G | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1975+2875T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94681830 | ||||||
chr5:94681945
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1975+2990A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94681945 | ||||||
chr5:94682007
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1975+3052C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94682007 | ||||||
chr5:94682040
|
G | A | 58 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(55): Show | 68 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1975+3085G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94682040 | ||||||
chr5:94682054
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02015.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1975+3099A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94682054 | ||||||
chr5:94682365
|
T | TA | 52 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(49): Show | 54 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1975+3418dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr5 | 94682365 | |||||
chr5:94682498
|
A | G | 1 | a0002c0002t0002g0241 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1975+3543A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94682498 | ||||||
chr5:94682861
|
A | G | 2 | a0001c0005t0004g0283a0001c0005t0004g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1976-3712A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94682861 | ||||||
chr5:94682868
|
A | G | 1 | a0001c0001t0006g0168 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1976-3705A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94682868 | ||||||
chr5:94682965
|
C | T | 4 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0091others(1): Show | 4 | HG02622.hp2 HG02723.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1976-3608C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94682965 | ||||||
chr5:94682979
|
T | C | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1976-3594T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94682979 | ||||||
chr5:94683041
|
C | T | 1 | a0001c0001t0003g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1976-3532C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94683041 | ||||||
chr5:94683136
|
T | C | 1 | a0001c0001t0001g0206 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1976-3437T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94683136 | ||||||
chr5:94683213
|
A | G | 1 | a0001c0001t0004g0047 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1976-3360A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94683213 | ||||||
chr5:94683397
|
C | T | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1976-3176C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94683397 | ||||||
chr5:94683448
|
C | T | 1 | a0001c0001t0003g0112 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1976-3125C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94683448 | ||||||
chr5:94683760
|
A | G | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1976-2813A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94683760 | ||||||
chr5:94684046
|
CATATTAA others(6): Show |
C | 1 | a0001c0001t0016g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1976-2526_1976-251 others(17): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684046 | ||||||
chr5:94684075
|
A | G | 210 | a0001c0001t0001g0219a0001c0001t0002g0227a0001c0001t0002g0255others(207): Show | 224 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1976-2498A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684075 | ||||||
chr5:94684121
|
T | C | 1 | a0001c0001t0007g0120 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1976-2452T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684121 | ||||||
chr5:94684432
|
G | C | 2 | a0002c0002t0005g0119a0002c0002t0005g0297 | 2 | NA18972.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1976-2141G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684432 | ||||||
chr5:94684480
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1976-2093C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684480 | ||||||
chr5:94684494
|
T | C | 1 | a0002c0002t0002g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1976-2079T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684494 | ||||||
chr5:94684504
|
C | G | 1 | a0001c0001t0002g0227 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1976-2069C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684504 | ||||||
chr5:94684505
|
T | C | 6 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(3): Show | 7 | HG01243.hp2 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1976-2068T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684505 | ||||||
chr5:94684514
|
C | T | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1976-2059C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684514 | ||||||
chr5:94684525
|
T | C | 56 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(53): Show | 58 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1976-2048T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684525 | ||||||
chr5:94684622
|
C | T | 1 | a0001c0005t0004g0283 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1976-1951C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684622 | ||||||
chr5:94684697
|
C | CA | 21 | a0001c0001t0001g0123a0001c0001t0001g0127a0001c0001t0001g0137others(18): Show | 21 | HG00423.hp1 HG00438.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1976-1850dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr5 | 94684697 | |||||
chr5:94684697
|
CA | C | 39 | a0001c0001t0001g0147a0001c0001t0001g0219a0001c0001t0001g0335others(36): Show | 40 | HG00673.hp2 HG00741.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1976-1850delA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr5 | 94684697 | |||||
chr5:94684697
|
CAA | C | 170 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0006others(167): Show | 181 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1976-1851_1976-185 others(6): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr5 | 94684697 | |||||
chr5:94684697
|
CAAA | C | 11 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0090others(8): Show | 13 | HG00738.hp1 HG01943.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1976-1852_1976-185 others(7): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr5 | 94684697 | |||||
chr5:94684932
|
G | A | 1 | a0002c0002t0005g0314 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1976-1641G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94684932 | ||||||
chr5:94685356
|
T | C | 56 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(53): Show | 58 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1976-1217T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94685356 | ||||||
chr5:94685512
|
T | C | 2 | a0002c0002t0005g0119a0002c0002t0005g0297 | 2 | NA18972.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1976-1061T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94685512 | ||||||
chr5:94685833
|
C | CA | 7 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0001g0137others(4): Show | 7 | HG02027.hp1 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1976-724dupA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr5 | 94685833 | |||||
chr5:94685906
|
A | G | 7 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0090others(4): Show | 7 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1976-667A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94685906 | ||||||
chr5:94685939
|
C | T | 1 | a0002c0002t0002g0238 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1976-634C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94685939 | ||||||
chr5:94686169
|
T | G | 56 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(53): Show | 58 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1976-404T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94686169 | ||||||
chr5:94686412
|
T | G | 4 | a0001c0001t0001g0319a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | NA18984.hp2 NA19010.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976-161T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94686412 | ||||||
chr5:94686523
|
A | C | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1976-50A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 15/20 | chr5 | 94686523 | ||||||
chr5:94686733
|
A | G | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2121+15A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94686733 | ||||||
chr5:94686786
|
TTTAG | T | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2121+72_2121+75del others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94686786 | |||||
chr5:94686826
|
C | T | 1 | a0001c0001t0001g0338 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2121+108C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94686826 | ||||||
chr5:94686827
|
G | A | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2121+109G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94686827 | ||||||
chr5:94686856
|
C | T | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.2121+138C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94686856 | ||||||
chr5:94686862
|
A | ACTGTAAG others(10): Show |
1 | a0001c0001t0003g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2121+146_2121+162d others(19): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94686862 | |||||
chr5:94686912
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2121+194C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94686912 | ||||||
chr5:94687016
|
G | A | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.2121+298G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687016 | ||||||
chr5:94687039
|
C | T | 1 | a0002c0002t0002g0265 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2121+321C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687039 | ||||||
chr5:94687196
|
C | T | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.2121+478C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687196 | ||||||
chr5:94687197
|
G | T | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.2121+479G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687197 | ||||||
chr5:94687199
|
G | C | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.2121+481G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687199 | ||||||
chr5:94687200
|
C | A | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.2121+482C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687200 | ||||||
chr5:94687211
|
TAGGTGAG others(7): Show |
T | 2 | a0001c0005t0004g0283a0001c0005t0004g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2121+507_2121+520d others(16): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94687211 | |||||
chr5:94687250
|
A | G | 23 | a0002c0002t0005g0013a0002c0002t0005g0119a0002c0002t0005g0295others(20): Show | 24 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.2121+532A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687250 | ||||||
chr5:94687383
|
G | T | 112 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(109): Show | 115 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.2121+665G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687383 | ||||||
chr5:94687587
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2121+869C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687587 | ||||||
chr5:94687646
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG03225.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2122-860A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687646 | ||||||
chr5:94687690
|
T | TCAACAA | 54 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0018others(51): Show | 56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.2122-791_2122-786d others(8): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94687690 | |||||
chr5:94687690
|
T | TCAACAAC others(2): Show |
7 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0016others(4): Show | 7 | HG01891.hp1 HG02698.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.2122-794_2122-786d others(11): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94687690 | |||||
chr5:94687690
|
TCAA | T | 53 | a0001c0001t0001g0187a0001c0001t0003g0006a0001c0001t0003g0068others(50): Show | 54 | HG00639.hp2 HG00741.hp1 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.2122-788_2122-786d others(5): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94687690 | |||||
chr5:94687690
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TCAACAAC others(5): Show |
T | 1 | a0001c0001t0001g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2122-797_2122-786d others(14): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94687690 | |||||
chr5:94687958
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TTAA | T | 4 | a0001c0001t0004g0028a0001c0001t0004g0057a0001c0001t0004g0058others(1): Show | 4 | HG00423.hp2 HG00438.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-540_2122-538d others(5): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94687958 | |||||
chr5:94687966
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A | T | 2 | a0001c0005t0004g0283a0001c0005t0004g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2122-540A>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94687966 | ||||||
chr5:94687971
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TTTA | T | 8 | a0001c0001t0007g0120a0001c0001t0007g0194a0001c0001t0007g0195others(5): Show | 8 | HG01978.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2122-525_2122-523d others(5): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94687971 | |||||
chr5:94688008
|
GTAGATAT others(29): Show |
G | 56 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(53): Show | 58 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2122-488_2122-453d others(38): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94688008 | |||||
chr5:94688022
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C | A | 27 | a0002c0002t0002g0002a0002c0002t0002g0008a0002c0002t0002g0009others(24): Show | 33 | HG00621.hp1 HG01978.hp2 HG02155.hp2 others(30): Show |
intron_variant | MODIFIER | c.2122-484C>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94688022 | ||||||
chr5:94688022
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CTATCTTT others(9): Show |
C | 3 | a0001c0001t0001g0209a0001c0001t0012g0189a0001c0001t0012g0190 | 3 | HG02976.hp1 HG03209.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.2122-468_2122-453d others(18): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr5 | 94688022 | |||||
chr5:94688311
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G | C | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2122-195G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 16/20 | chr5 | 94688311 | ||||||
chr5:94689036
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A | ACCT | 323 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(320): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.2285+369_2285+371d others(5): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr5 | 94689036 | |||||
chr5:94689085
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A | G | 1 | a0001c0001t0001g0142 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2286-388A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 17/20 | chr5 | 94689085 | ||||||
chr5:94689102
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G | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2286-371G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 17/20 | chr5 | 94689102 | ||||||
chr5:94689146
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G | A | 94 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(91): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2286-327G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 17/20 | chr5 | 94689146 | ||||||
chr5:94689290
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T | C | 1 | a0001c0001t0025g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2286-183T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 17/20 | chr5 | 94689290 | ||||||
chr5:94689342
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A | C | 11 | a0001c0001t0001g0020a0001c0001t0001g0139a0001c0001t0001g0178others(8): Show | 11 | HG00642.hp2 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2286-131A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 17/20 | chr5 | 94689342 | ||||||
chr5:94689820
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C | T | 2 | a0001c0001t0016g0193a0001c0001t0016g0289 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2419+214C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | chr5 | 94689820 | ||||||
chr5:94690014
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G | A | 1 | a0001c0001t0007g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2419+408G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | chr5 | 94690014 | ||||||
chr5:94690739
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T | G | 1 | a0001c0001t0007g0194 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2420-825T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | chr5 | 94690739 | ||||||
chr5:94690758
|
TA | T | 54 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(51): Show | 56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.2420-804delA | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr5 | 94690758 | |||||
chr5:94690822
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G | A | 3 | a0001c0001t0010g0065a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02922.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2420-742G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | chr5 | 94690822 | ||||||
chr5:94690901
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AT | A | 8 | a0001c0001t0007g0120a0001c0001t0007g0194a0001c0001t0007g0195others(5): Show | 8 | HG01496.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2420-649delT | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr5 | 94690901 | |||||
chr5:94690932
|
C | CTG | 93 | a0001c0001t0002g0227a0001c0001t0002g0255a0001c0001t0003g0074others(90): Show | 103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.2420-613_2420-612d others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr5 | 94690932 | |||||
chr5:94690932
|
C | CTGTG | 4 | a0001c0001t0012g0189a0001c0001t0012g0190a0002c0002t0002g0009others(1): Show | 5 | HG00639.hp1 HG02976.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2420-615_2420-612d others(6): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr5 | 94690932 | |||||
chr5:94691300
|
A | G | 1 | a0002c0002t0005g0314 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2420-264A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | chr5 | 94691300 | ||||||
chr5:94691306
|
G | A | 53 | a0001c0001t0003g0006a0001c0001t0003g0068a0001c0001t0003g0069others(50): Show | 54 | HG00741.hp1 HG01099.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.2420-258G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | chr5 | 94691306 | ||||||
chr5:94691372
|
G | T | 1 | a0001c0001t0001g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2420-192G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 18/20 | chr5 | 94691372 | ||||||
chr5:94691813
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2512+157T>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 19/20 | chr5 | 94691813 | ||||||
chr5:94692504
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2695+248G>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94692504 | ||||||
chr5:94692749
|
G | A | 3 | a0001c0001t0001g0334a0001c0001t0001g0341a0005c0010t0001g0339 | 3 | HG03704.hp2 NA19007.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2695+493G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94692749 | ||||||
chr5:94693482
|
G | A | 1 | a0002c0002t0002g0257 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2695+1226G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94693482 | ||||||
chr5:94693787
|
A | G | 71 | a0001c0001t0002g0227a0001c0001t0002g0255a0002c0002t0002g0002others(68): Show | 81 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.2696-1044A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94693787 | ||||||
chr5:94693845
|
T | G | 1 | a0002c0002t0020g0254 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2696-986T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94693845 | ||||||
chr5:94693846
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2696-985C>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94693846 | ||||||
chr5:94693861
|
T | G | 1 | a0007c0013t0023g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2696-970T>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94693861 | ||||||
chr5:94693939
|
CAG | C | 54 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0014others(51): Show | 56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.2696-889_2696-888d others(4): Show |
SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr5 | 94693939 | |||||
chr5:94693980
|
C | G | 1 | a0001c0001t0019g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2696-851C>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94693980 | ||||||
chr5:94694087
|
A | C | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2696-744A>C | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94694087 | ||||||
chr5:94694146
|
A | G | 1 | a0001c0001t0004g0040 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2696-685A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94694146 | ||||||
chr5:94694390
|
G | T | 1 | a0001c0001t0003g0100 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2696-441G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94694390 | ||||||
chr5:94694475
|
A | G | 3 | a0001c0001t0016g0193a0001c0001t0016g0289a0007c0013t0023g0269 | 3 | HG02055.hp1 HG03017.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2696-356A>G | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94694475 | ||||||
chr5:94694520
|
G | A | 1 | a0002c0002t0002g0241 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2696-311G>A | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94694520 | ||||||
chr5:94694698
|
G | T | 2 | a0001c0001t0015g0281a0001c0001t0015g0282 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2696-133G>T | SLF1 | ENSG00000133302.13 | transcript | ENST00000265140.10 | protein_coding | 20/20 | chr5 | 94694698 |