geneid | 10590 |
---|---|
ensemblid | ENSG00000079689.15 |
hgncid | 16941 |
symbol | SCGN |
name | secretagogin, EF-hand calcium binding protein |
refseq_nuc | NM_006998.4 |
refseq_prot | NP_008929.2 |
ensembl_nuc | ENST00000377961.3 |
ensembl_prot | ENSP00000367197.2 |
mane_status | MANE Select |
chr | chr6 |
start | 25652215 |
end | 25701783 |
strand | + |
ver | v1.2 |
region | chr6:25652215-25701783 |
region5000 | chr6:25647215-25706783 |
regionname0 | SCGN_chr6_25652215_25701783 |
regionname5000 | SCGN_chr6_25647215_25706783 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 276 | 350 | 77 | 65 | 149 | 17 | 40 | 116 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0002 | 0/0 | 276 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0003 | 0/0 | 276 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0004 | 0/0 | 276 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0005 | 0/0 | 276 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0006 | 0/0 | 276 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0007 | 0/0 | 276 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0008 | 0/0 | 276 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0009 | 0/0 | 276 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 831 | 346 | 76 | 65 | 146 | 17 | 40 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
c0002 | 0/0 | 831 | 6 | 6 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
c0003 | 0/0 | 831 | 5 | 5 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
c0004 | 0/0 | 831 | 3 | 0 | 0 | 3 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
c0005 | 0/0 | 831 | 2 | 1 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
c0006 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
c0007 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
c0008 | 0/0 | 831 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
c0009 | 0/0 | 831 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
c0010 | 0/0 | 831 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
c0011 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 639 | 112 | 9 | 21 | 73 | 5 | 4 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0002 | 0/1 | 639 | 82 | 24 | 10 | 23 | 6 | 18 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0003 | 0/0 | 639 | 65 | 36 | 13 | 4 | 4 | 8 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0004 | 0/0 | 638 | 41 | 0 | 13 | 23 | 1 | 4 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0005 | 0/0 | 638 | 26 | 2 | 4 | 14 | 1 | 5 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0006 | 0/0 | 638 | 18 | 3 | 1 | 10 | 1 | 3 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0007 | 0/0 | 637 | 6 | 6 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0008 | 0/0 | 639 | 6 | 3 | 3 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0009 | 0/0 | 638 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0010 | 1/0 | 638 | 2 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0011 | 0/0 | 637 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0012 | 0/0 | 638 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0013 | 0/0 | 639 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0014 | 0/0 | 639 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0015 | 0/0 | 639 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0016 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0017 | 0/0 | 639 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
t0018 | 0/0 | 639 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0054 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 831 | 346 | 76 | 65 | 146 | 17 | 40 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0004 | 0/0 | 831 | 3 | 0 | 0 | 3 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0006 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0002c0002 | 0/0 | 831 | 6 | 6 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0003c0003 | 0/0 | 831 | 5 | 5 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0004c0005 | 0/0 | 831 | 2 | 1 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0005c0007 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0006c0008 | 0/0 | 831 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0007c0009 | 0/0 | 831 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0008c0010 | 0/0 | 831 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0009c0011 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1469 | 108 | 9 | 21 | 71 | 4 | 3 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0002 | 0/1 | 1469 | 81 | 24 | 10 | 22 | 6 | 18 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0003 | 0/0 | 1469 | 51 | 23 | 13 | 4 | 4 | 7 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0004 | 0/0 | 1468 | 39 | 0 | 12 | 22 | 1 | 4 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0005 | 0/0 | 1468 | 26 | 2 | 4 | 14 | 1 | 5 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0006 | 0/0 | 1468 | 18 | 3 | 1 | 10 | 1 | 3 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0007 | 0/0 | 1467 | 6 | 6 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0008 | 0/0 | 1469 | 6 | 3 | 3 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0009 | 0/0 | 1468 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0010 | 1/0 | 1468 | 2 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0012 | 0/0 | 1468 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0013 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0014 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0015 | 0/0 | 1469 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0016 | 0/0 | 1468 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0017 | 0/0 | 1469 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0001t0018 | 0/0 | 1469 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0004t0001 | 0/0 | 1469 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0004t0004 | 0/0 | 1468 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0001c0006t0003 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0002c0002t0003 | 0/0 | 1469 | 6 | 6 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0003c0003t0003 | 0/0 | 1469 | 5 | 5 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0004c0005t0004 | 0/0 | 1468 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0004c0005t0011 | 0/0 | 1467 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0005c0007t0002 | 0/0 | 1469 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0006c0008t0001 | 0/0 | 1469 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0007c0009t0001 | 0/0 | 1469 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0008c0010t0003 | 0/0 | 1469 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
a0009c0011t0003 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | copy fasta | chr6 | 25647215 | 25706783 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0054 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0006g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0007g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0008g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0008g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0010g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0012g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0013g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0014g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0015g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0016g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0017g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0001t0018g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0004t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0001c0006t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0002c0002t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0002c0002t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0002c0002t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0002c0002t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0002c0002t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0003c0003t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0003c0003t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0003c0003t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0003c0003t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0004c0005t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0004c0005t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0005c0007t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0006c0008t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0007c0009t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0008c0010t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
a0009c0011t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0273 | EUR | GBR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0176 | EUR | GBR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | GBR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0097 | EUR | FIN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00323 | hp1 | a0006 | c0008 | t0001 | g0192 | EUR | FIN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0322 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00609 | hp1 | a0005 | c0007 | t0002 | g0207 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0017 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00673 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0295 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0017 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0271 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0332 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0320 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0296 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0298 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01361 | hp1 | a0001 | c0001 | t0008 | g0204 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0315 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0311 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0260 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0083 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0084 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01884 | hp2 | a0003 | c0003 | t0003 | g0329 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01891 | hp2 | a0003 | c0003 | t0003 | g0027 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0308 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0302 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01993 | hp1 | a0001 | c0001 | t0017 | g0070 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0314 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0161 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0286 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0267 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0301 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CDX | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02257 | hp1 | a0003 | c0003 | t0003 | g0027 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02257 | hp2 | a0001 | c0006 | t0003 | g0046 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02280 | hp2 | a0003 | c0003 | t0003 | g0330 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02300 | hp2 | a0004 | c0005 | t0004 | g0293 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02572 | hp2 | a0002 | c0002 | t0003 | g0117 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0304 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0252 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0333 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02818 | hp2 | a0002 | c0002 | t0003 | g0094 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0057 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02896 | hp2 | a0002 | c0002 | t0003 | g0115 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0250 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02922 | hp2 | a0004 | c0005 | t0011 | g0264 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0262 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03017 | hp1 | a0007 | c0009 | t0001 | g0013 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0313 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0254 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0266 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0162 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0331 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03195 | hp1 | a0003 | c0003 | t0003 | g0328 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03209 | hp1 | a0009 | c0011 | t0003 | g0336 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0225 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0297 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0116 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03490 | hp1 | a0001 | c0001 | t0005 | g0255 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0268 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03516 | hp2 | a0001 | c0001 | t0013 | g0120 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03579 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0289 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03669 | hp1 | a0008 | c0010 | t0003 | g0034 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0256 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0285 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0306 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0160 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0305 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0146 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0307 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | YRI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | YRI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18940 | hp1 | a0001 | c0001 | t0006 | g0318 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0309 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18948 | hp2 | a0001 | c0004 | t0004 | g0291 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18956 | hp2 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18957 | hp1 | a0001 | c0001 | t0006 | g0327 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18957 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18959 | hp2 | a0001 | c0001 | t0006 | g0299 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18965 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18974 | hp2 | a0001 | c0004 | t0001 | g0127 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18977 | hp1 | a0001 | c0001 | t0018 | g0126 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18979 | hp2 | a0001 | c0001 | t0015 | g0135 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18982 | hp1 | a0001 | c0001 | t0006 | g0300 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18983 | hp1 | a0001 | c0004 | t0001 | g0103 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18987 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0325 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19030 | hp2 | a0001 | c0001 | t0016 | g0087 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0334 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19054 | hp1 | a0001 | c0001 | t0005 | g0310 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19055 | hp1 | a0001 | c0001 | t0012 | g0316 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19056 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19058 | hp1 | a0001 | c0001 | t0006 | g0317 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19075 | hp2 | a0001 | c0001 | t0005 | g0321 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19089 | hp2 | a0001 | c0001 | t0006 | g0323 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | YRI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0253 | AFR | YRI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ASW | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | ASW | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0085 | EUR | TSI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0104 | EUR | TSI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0265 | EUR | TSI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0233 | EUR | TSI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | GIH | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA20905 | hp2 | a0001 | c0001 | t0005 | g0278 | SAS | GIH | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0263 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0219 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | USA | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0275 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0054 | REF | REF | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0010 | g0195 | REF | REF | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:25653400
|
A | T | 1 | a0009 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.101A>T | p.Glu34Val | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/11 | 290/1468 | 101/831 | 34/276 | chr6 | 25653400 | ||
chr6:25661633
|
C | T | 1 | a0008 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.235C>T | p.Arg79Trp | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/11 | 424/1468 | 235/831 | 79/276 | chr6 | 25661633 | ||
chr6:25664994
|
C | T | 1 | a0007 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.298C>T | p.Arg100Trp | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/11 | 487/1468 | 298/831 | 100/276 | chr6 | 25664994 | ||
chr6:25669566
|
G | A | 1 | a0004 | 2 | HG02300.hp2 HG02922.hp2 |
missense_variant&splice_region_variant | MODERATE | c.392G>A | p.Arg131His | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 5/11 | 581/1468 | 392/831 | 131/276 | chr6 | 25669566 | ||
chr6:25670014
|
C | G | 1 | a0006 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.409C>G | p.Leu137Val | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/11 | 598/1468 | 409/831 | 137/276 | chr6 | 25670014 | ||
chr6:25670035
|
G | C | 1 | a0005 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.430G>C | p.Ala144Pro | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/11 | 619/1468 | 430/831 | 144/276 | chr6 | 25670035 | ||
chr6:25691069
|
C | T | 1 | a0003 | 5 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(2): Show |
missense_variant | MODERATE | c.647C>T | p.Ala216Val | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/11 | 836/1468 | 647/831 | 216/276 | chr6 | 25691069 | ||
chr6:25701256
|
G | A | 1 | a0002 | 6 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.752G>A | p.Arg251His | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 941/1468 | 752/831 | 251/276 | chr6 | 25701256 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:25669555
|
T | C | 1 | a0001c0006 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.381T>C | p.Ala127Ala | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 5/11 | 570/1468 | 381/831 | 127/276 | chr6 | 25669555 | ||
chr6:25691124
|
G | A | 1 | a0001c0004 | 3 | NA18948.hp2 NA18974.hp2 NA18983.hp1 |
splice_region_variant&synonymous_variant | LOW | c.702G>A | p.Gln234Gln | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/11 | 891/1468 | 702/831 | 234/276 | chr6 | 25691124 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:25652340
|
AG | A | 9 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(6): Show | 95 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
5_prime_UTR_variant | MODIFIER | c.-62delG | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/11 | 62 | INFO_REALIGN_3_PRIME | chr6 | 25652340 | ||||
chr6:25701439
|
T | C | 1 | a0001c0001t0013 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*104T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 104 | chr6 | 25701439 | |||||
chr6:25701463
|
C | G | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
3_prime_UTR_variant | MODIFIER | c.*128C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 128 | chr6 | 25701463 | |||||
chr6:25701470
|
G | T | 2 | a0001c0001t0008a0001c0001t0009 | 8 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*135G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 135 | chr6 | 25701470 | |||||
chr6:25701490
|
G | A | 8 | a0001c0001t0001a0001c0001t0004a0001c0001t0014others(5): Show | 154 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*155G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 155 | chr6 | 25701490 | |||||
chr6:25701630
|
G | T | 2 | a0001c0001t0012a0001c0001t0018 | 2 | NA18977.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*295G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 295 | chr6 | 25701630 | |||||
chr6:25701675
|
G | A | 10 | a0001c0001t0003a0001c0001t0006a0001c0001t0015others(7): Show | 86 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*340G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 340 | chr6 | 25701675 | |||||
chr6:25701676
|
T | C | 1 | a0001c0001t0015 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 341 | chr6 | 25701676 | |||||
chr6:25701692
|
T | A | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 357 | chr6 | 25701692 | |||||
chr6:25701739
|
A | AT | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
3_prime_UTR_variant | MODIFIER | c.*411dupT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 412 | INFO_REALIGN_3_PRIME | chr6 | 25701739 | ||||
chr6:25701747
|
G | T | 1 | a0001c0001t0017 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 412 | chr6 | 25701747 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:25652499
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0003g0028 | 3 | HG02572.hp1 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.82+14G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25652499 | ||||||
chr6:25652644
|
T | C | 1 | a0001c0001t0004g0031 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.82+159T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25652644 | ||||||
chr6:25652741
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.82+256A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25652741 | ||||||
chr6:25652852
|
TCA | T | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.82+369_82+370delAC | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 25652852 | |||||
chr6:25652862
|
G | T | 94 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(91): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.82+377G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25652862 | ||||||
chr6:25653047
|
C | T | 7 | a0001c0001t0002g0331a0001c0001t0002g0333a0001c0001t0003g0332others(4): Show | 8 | HG01106.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-335C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653047 | ||||||
chr6:25653173
|
A | G | 14 | a0001c0001t0001g0019a0001c0001t0001g0237a0001c0001t0001g0238others(11): Show | 15 | HG00140.hp2 HG00280.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.83-209A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653173 | ||||||
chr6:25653208
|
T | G | 28 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0033others(25): Show | 29 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.83-174T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653208 | ||||||
chr6:25653220
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.83-162C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653220 | ||||||
chr6:25653236
|
T | G | 6 | a0001c0001t0005g0251a0001c0001t0007g0004a0001c0001t0007g0252others(3): Show | 8 | HG01884.hp1 HG02109.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-146T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653236 | ||||||
chr6:25653317
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-65T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653317 | ||||||
chr6:25653334
|
G | A | 1 | a0001c0001t0005g0255 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.83-48G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653334 | ||||||
chr6:25653338
|
T | TA | 94 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(91): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.83-44_83-43insA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653338 | ||||||
chr6:25653380
|
AG | A | 4 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0235others(1): Show | 7 | HG02486.hp1 HG02615.hp2 HG02965.hp1 others(4): Show |
splice_acceptor_variant&intron_variant | HIGH | c.83-1delG | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653380 | ||||||
chr6:25653484
|
G | A | 1 | a0001c0001t0008g0057 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.153+32G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653484 | ||||||
chr6:25653501
|
G | A | 1 | a0001c0001t0004g0256 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.153+49G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653501 | ||||||
chr6:25653597
|
T | C | 11 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0002g0006others(8): Show | 13 | HG01175.hp2 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+145T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653597 | ||||||
chr6:25653607
|
T | C | 1 | a0001c0001t0005g0257 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.153+155T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653607 | ||||||
chr6:25653614
|
T | G | 94 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(91): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.153+162T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653614 | ||||||
chr6:25653633
|
T | A | 1 | a0001c0001t0003g0334 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153+181T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653633 | ||||||
chr6:25653861
|
C | G | 33 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0033others(30): Show | 34 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.153+409C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653861 | ||||||
chr6:25653920
|
G | T | 1 | a0001c0001t0001g0232 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.153+468G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653920 | ||||||
chr6:25654000
|
T | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0002g0001others(21): Show | 30 | HG01243.hp1 HG01891.hp1 HG01993.hp1 others(27): Show |
intron_variant | MODIFIER | c.153+548T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654000 | ||||||
chr6:25654037
|
T | A | 111 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 123 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.153+585T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654037 | ||||||
chr6:25654120
|
C | G | 1 | a0001c0001t0006g0327 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.153+668C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654120 | ||||||
chr6:25654120
|
C | T | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231 | 3 | HG01167.hp2 HG01169.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.153+668C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654120 | ||||||
chr6:25654231
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.153+779C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654231 | ||||||
chr6:25654326
|
G | T | 2 | a0001c0001t0002g0228a0001c0001t0003g0227 | 2 | HG01358.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.153+874G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654326 | ||||||
chr6:25654358
|
G | T | 1 | a0001c0001t0004g0326 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.153+906G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654358 | ||||||
chr6:25654397
|
C | G | 2 | a0001c0001t0005g0324a0001c0001t0005g0325 | 2 | NA19011.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.153+945C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654397 | ||||||
chr6:25654489
|
T | C | 3 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085 | 3 | HG01516.hp2 HG01517.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.153+1037T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654489 | ||||||
chr6:25654680
|
CCT | C | 3 | a0001c0001t0001g0053a0001c0001t0002g0054a0001c0001t0002g0055 | 3 | HG00741.hp2 HG01074.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.153+1229_153+1230d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654680 | ||||||
chr6:25654759
|
C | T | 94 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(91): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.153+1307C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654759 | ||||||
chr6:25654771
|
T | C | 1 | a0001c0001t0004g0258 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.153+1319T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654771 | ||||||
chr6:25654829
|
G | T | 2 | a0001c0001t0002g0226a0001c0001t0010g0225 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153+1377G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654829 | ||||||
chr6:25654831
|
C | T | 11 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0002g0006others(8): Show | 13 | HG01175.hp2 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+1379C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654831 | ||||||
chr6:25654833
|
G | T | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153+1381G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654833 | ||||||
chr6:25654876
|
T | C | 94 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(91): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.153+1424T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654876 | ||||||
chr6:25654933
|
G | A | 2 | a0001c0001t0002g0226a0001c0001t0010g0225 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153+1481G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654933 | ||||||
chr6:25654950
|
A | T | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153+1498A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654950 | ||||||
chr6:25655013
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.153+1561C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655013 | ||||||
chr6:25655061
|
C | A | 2 | a0001c0001t0003g0086a0001c0001t0016g0087 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.153+1609C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655061 | ||||||
chr6:25655067
|
A | G | 1 | a0001c0001t0002g0005 | 2 | HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.153+1615A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655067 | ||||||
chr6:25655194
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.153+1742G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655194 | ||||||
chr6:25655303
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.153+1851T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655303 | ||||||
chr6:25655447
|
G | A | 94 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(91): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.153+1995G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655447 | ||||||
chr6:25655611
|
T | G | 94 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(91): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.153+2159T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655611 | ||||||
chr6:25655665
|
A | AT | 86 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(83): Show | 95 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.153+2220dupT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25655665 | |||||
chr6:25655695
|
C | G | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.153+2243C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655695 | ||||||
chr6:25655699
|
T | C | 1 | a0001c0001t0005g0260 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.153+2247T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655699 | ||||||
chr6:25655867
|
T | G | 2 | a0001c0001t0008g0161a0001c0001t0008g0162 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.153+2415T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655867 | ||||||
chr6:25655984
|
G | A | 1 | a0001c0001t0004g0261 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.153+2532G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655984 | ||||||
chr6:25656293
|
A | G | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.153+2841A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25656293 | ||||||
chr6:25656433
|
C | G | 80 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(77): Show | 89 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.153+2981C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25656433 | ||||||
chr6:25656466
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG01261.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.153+3014A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25656466 | ||||||
chr6:25656485
|
T | C | 1 | a0001c0001t0003g0032 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.153+3033T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25656485 | ||||||
chr6:25656747
|
G | A | 3 | a0001c0001t0002g0058a0001c0001t0002g0065a0001c0001t0002g0066 | 3 | HG02630.hp1 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.153+3295G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25656747 | ||||||
chr6:25657058
|
C | T | 3 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0052 | 3 | HG01346.hp2 HG01433.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.153+3606C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657058 | ||||||
chr6:25657063
|
A | G | 8 | a0001c0001t0003g0015a0001c0001t0003g0083a0001c0001t0003g0084others(5): Show | 9 | HG01255.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+3611A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657063 | ||||||
chr6:25657175
|
A | T | 30 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0033others(27): Show | 31 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.153+3723A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657175 | ||||||
chr6:25657235
|
A | C | 294 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(291): Show | 321 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.153+3783A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657235 | ||||||
chr6:25657312
|
A | G | 294 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(291): Show | 321 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.153+3860A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657312 | ||||||
chr6:25657334
|
A | G | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153+3882A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657334 | ||||||
chr6:25657362
|
A | G | 45 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(42): Show | 51 | HG00408.hp1 HG00738.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.153+3910A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657362 | ||||||
chr6:25657482
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.153+4030G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657482 | ||||||
chr6:25657534
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.154-4018G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657534 | ||||||
chr6:25657617
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0237a0001c0001t0001g0238others(9): Show | 13 | HG00140.hp2 HG00280.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-3935G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657617 | ||||||
chr6:25657657
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0002g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154-3893_154-3870d others(26): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25657657 | |||||
chr6:25657681
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0005g0263a0001c0001t0009g0262 | 3 | HG02486.hp2 HG02970.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.154-3871G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657681 | ||||||
chr6:25657685
|
A | G | 9 | a0001c0001t0002g0163a0001c0001t0002g0196a0001c0001t0002g0197others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-3867A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657685 | ||||||
chr6:25657808
|
C | T | 1 | a0001c0001t0004g0288 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.154-3744C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657808 | ||||||
chr6:25657822
|
G | A | 6 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0008g0017others(3): Show | 7 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-3730G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657822 | ||||||
chr6:25657883
|
C | T | 4 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0228others(1): Show | 4 | HG01358.hp1 HG01496.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-3669C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657883 | ||||||
chr6:25657995
|
A | G | 1 | a0001c0001t0005g0260 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.154-3557A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657995 | ||||||
chr6:25658002
|
CCTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0259 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.154-3549_154-3539d others(13): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658002
|
CCTTTTTT others(8): Show |
C | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154-3549_154-3535d others(17): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658002
|
CCTTTTTT others(16): Show |
C | 1 | a0001c0001t0006g0323 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.154-3549_154-3527d others(25): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658002
|
CCTTTTTT others(17): Show |
C | 11 | a0001c0001t0004g0319a0001c0001t0004g0320a0001c0001t0005g0257others(8): Show | 13 | HG00408.hp1 HG01109.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-3549_154-3526d others(26): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658002
|
CCTTTTTT others(18): Show |
C | 33 | a0001c0001t0002g0331a0001c0001t0002g0333a0001c0001t0003g0332others(30): Show | 37 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.154-3549_154-3525d others(27): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658002
|
CCTTTTTT others(19): Show |
C | 11 | a0001c0001t0004g0258a0001c0001t0004g0283a0001c0001t0004g0284others(8): Show | 11 | HG02074.hp1 HG02300.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-3549_154-3524d others(28): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658002
|
CCTTTTTT others(20): Show |
C | 29 | a0001c0001t0004g0031a0001c0001t0004g0256a0001c0001t0004g0265others(26): Show | 32 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.154-3549_154-3523d others(29): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658002
|
CCTTTTTT others(21): Show |
C | 5 | a0001c0001t0002g0049a0001c0001t0002g0055a0001c0001t0004g0261others(2): Show | 5 | HG00741.hp2 HG02922.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-3549_154-3522d others(30): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658002
|
CCTTTTTT others(22): Show |
C | 5 | a0001c0001t0001g0053a0001c0001t0002g0047a0001c0001t0002g0048others(2): Show | 5 | HG01074.hp1 HG02080.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-3549_154-3521d others(31): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658002
|
CCTTTTTT others(23): Show |
C | 17 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0040others(14): Show | 18 | HG00323.hp2 HG00733.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.154-3549_154-3520d others(32): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658002
|
CCTTTTTT others(28): Show |
C | 1 | a0001c0001t0005g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.154-3549_154-3515d others(37): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | ||||||
chr6:25658003
|
CTTT | C | 13 | a0001c0001t0001g0183a0001c0001t0001g0187a0001c0001t0001g0212others(10): Show | 13 | HG00280.hp1 HG01192.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-3497_154-3495d others(5): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTT | C | 16 | a0001c0001t0001g0174a0001c0001t0001g0177a0001c0001t0001g0180others(13): Show | 16 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.154-3498_154-3495d others(6): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTT | C | 11 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0241others(8): Show | 11 | HG01943.hp1 HG01993.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-3499_154-3495d others(7): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0014a0001c0001t0001g0156a0001c0001t0001g0239others(3): Show | 7 | HG02630.hp1 HG02717.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-3502_154-3495d others(10): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(2): Show |
C | 8 | a0001c0001t0001g0019a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 9 | HG01081.hp1 HG02155.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-3503_154-3495d others(11): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0002g0150others(4): Show | 7 | HG01517.hp2 HG03195.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-3504_154-3495d others(12): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(4): Show |
C | 14 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(11): Show | 17 | HG00621.hp1 HG01255.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.154-3505_154-3495d others(13): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(5): Show |
C | 48 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0088others(45): Show | 52 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.154-3506_154-3495d others(14): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(6): Show |
C | 35 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0064others(32): Show | 39 | HG00280.hp2 HG00408.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.154-3507_154-3495d others(15): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(7): Show |
C | 9 | a0001c0001t0001g0029a0001c0001t0001g0059a0001c0001t0002g0006others(6): Show | 12 | HG01515.hp1 HG01517.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-3508_154-3495d others(16): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0001g0030a0001c0001t0003g0234a0003c0003t0003g0328others(1): Show | 4 | HG01884.hp2 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-3509_154-3495d others(17): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0003g0032 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.154-3510_154-3495d others(18): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0002g0169a0001c0001t0002g0335 | 2 | HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.154-3515_154-3495d others(23): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0002g0168a0009c0011t0003g0336 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.154-3516_154-3495d others(24): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0003g0334 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154-3517_154-3495d others(25): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(17): Show |
C | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG01070.hp1 HG01071.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.154-3518_154-3495d others(26): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(18): Show |
C | 2 | a0001c0001t0002g0228a0001c0001t0003g0227 | 2 | HG01358.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.154-3519_154-3495d others(27): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(20): Show |
C | 1 | a0005c0007t0002g0207 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.154-3521_154-3495d others(29): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(22): Show |
C | 6 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0002g0221others(3): Show | 6 | HG01167.hp2 HG01496.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-3523_154-3495d others(31): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(23): Show |
C | 2 | a0001c0001t0001g0164a0001c0001t0003g0229 | 2 | HG01069.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.154-3524_154-3495d others(32): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(26): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.154-3527_154-3495d others(35): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(29): Show |
C | 7 | a0001c0001t0002g0233a0001c0001t0003g0205a0001c0001t0003g0206others(4): Show | 8 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-3530_154-3495d others(38): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658003
|
CTTTTTTT others(31): Show |
C | 1 | a0001c0001t0002g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.154-3532_154-3495d others(40): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | |||||
chr6:25658149
|
C | T | 1 | a0001c0001t0005g0315 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.154-3403C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658149 | ||||||
chr6:25658186
|
C | T | 90 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(87): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.154-3366C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658186 | ||||||
chr6:25658197
|
G | A | 6 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(3): Show | 6 | HG01106.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-3355G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658197 | ||||||
chr6:25658267
|
C | A | 2 | a0001c0001t0003g0086a0001c0001t0016g0087 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.154-3285C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658267 | ||||||
chr6:25658352
|
T | C | 48 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0064others(45): Show | 51 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.154-3200T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658352 | ||||||
chr6:25658405
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154-3147T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658405 | ||||||
chr6:25658490
|
G | A | 3 | a0001c0001t0002g0331a0001c0001t0002g0333a0001c0001t0003g0332 | 3 | HG01106.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.154-3062G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658490 | ||||||
chr6:25658547
|
A | T | 3 | a0001c0001t0001g0211a0001c0001t0001g0217a0005c0007t0002g0207 | 3 | HG00609.hp1 HG02135.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.154-3005A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658547 | ||||||
chr6:25658679
|
T | C | 86 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(83): Show | 95 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.154-2873T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658679 | ||||||
chr6:25658793
|
CA | C | 92 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(89): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.154-2753delA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658793 | |||||
chr6:25658812
|
A | G | 6 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0008g0017others(3): Show | 7 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-2740A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658812 | ||||||
chr6:25658901
|
A | G | 2 | a0001c0001t0002g0228a0001c0001t0003g0227 | 2 | HG01358.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.154-2651A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658901 | ||||||
chr6:25658923
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.154-2629T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658923 | ||||||
chr6:25658944
|
G | A | 48 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0064others(45): Show | 51 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.154-2608G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658944 | ||||||
chr6:25658991
|
G | A | 92 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(89): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.154-2561G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658991 | ||||||
chr6:25659031
|
G | A | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154-2521G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659031 | ||||||
chr6:25659042
|
T | C | 1 | a0001c0001t0003g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.154-2510T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659042 | ||||||
chr6:25659077
|
C | T | 31 | a0001c0001t0001g0019a0001c0001t0001g0211a0001c0001t0001g0212others(28): Show | 32 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.154-2475C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659077 | ||||||
chr6:25659094
|
C | G | 1 | a0001c0001t0005g0314 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.154-2458C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659094 | ||||||
chr6:25659203
|
G | T | 2 | a0001c0001t0002g0226a0001c0001t0010g0225 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.154-2349G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659203 | ||||||
chr6:25659525
|
G | T | 1 | a0001c0001t0003g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.154-2027G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659525 | ||||||
chr6:25659609
|
T | C | 2 | a0001c0001t0003g0086a0001c0001t0016g0087 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.154-1943T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659609 | ||||||
chr6:25659725
|
C | A | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154-1827C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659725 | ||||||
chr6:25659763
|
T | C | 6 | a0001c0001t0002g0093a0002c0002t0003g0009a0002c0002t0003g0094others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-1789T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659763 | ||||||
chr6:25659787
|
CCAGGCTA others(1661): Show |
C | 1 | a0001c0001t0004g0261 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.154-1762_154-95del | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25659787 | |||||
chr6:25659825
|
G | C | 2 | a0001c0001t0003g0086a0001c0001t0016g0087 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.154-1727G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659825 | ||||||
chr6:25659930
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00323.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.154-1622C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659930 | ||||||
chr6:25659969
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.154-1583G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659969 | ||||||
chr6:25660079
|
A | G | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-1473A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660079 | ||||||
chr6:25660119
|
G | A | 4 | a0003c0003t0003g0027a0003c0003t0003g0328a0003c0003t0003g0329others(1): Show | 5 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-1433G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660119 | ||||||
chr6:25660123
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.154-1429G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660123 | ||||||
chr6:25660263
|
C | A | 2 | a0001c0001t0005g0263a0001c0001t0009g0262 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.154-1289C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660263 | ||||||
chr6:25660282
|
G | A | 92 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(89): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.154-1270G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660282 | ||||||
chr6:25660414
|
G | T | 1 | a0004c0005t0004g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.154-1138G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660414 | ||||||
chr6:25660422
|
T | G | 1 | a0001c0001t0001g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.154-1130T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660422 | ||||||
chr6:25660545
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.154-1007G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660545 | ||||||
chr6:25660580
|
C | T | 40 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0033others(37): Show | 43 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.154-972C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660580 | ||||||
chr6:25660659
|
C | T | 1 | a0001c0001t0004g0282 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.154-893C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660659 | ||||||
chr6:25660744
|
A | G | 91 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(88): Show | 100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.154-808A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660744 | ||||||
chr6:25660836
|
G | A | 91 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(88): Show | 100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.154-716G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660836 | ||||||
chr6:25660899
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0003g0227 | 2 | HG01358.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.154-653C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660899 | ||||||
chr6:25661140
|
A | C | 91 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(88): Show | 100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.154-412A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25661140 | ||||||
chr6:25661321
|
T | C | 28 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0033others(25): Show | 29 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.154-231T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25661321 | ||||||
chr6:25661470
|
T | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.154-82T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25661470 | ||||||
chr6:25661659
|
A | T | 90 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(87): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.246+15A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661659 | ||||||
chr6:25661735
|
A | G | 1 | a0001c0001t0002g0233 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.246+91A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661735 | ||||||
chr6:25661756
|
T | G | 1 | a0001c0001t0002g0233 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.246+112T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661756 | ||||||
chr6:25661914
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.246+270A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661914 | ||||||
chr6:25661932
|
C | G | 1 | a0001c0001t0004g0313 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.246+288C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661932 | ||||||
chr6:25661946
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+302A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661946 | ||||||
chr6:25661948
|
C | A | 1 | a0001c0001t0002g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+304C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661948 | ||||||
chr6:25661951
|
C | A | 1 | a0001c0001t0002g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+307C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661951 | ||||||
chr6:25661952
|
T | A | 1 | a0001c0001t0002g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+308T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661952 | ||||||
chr6:25661953
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+309A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661953 | ||||||
chr6:25661954
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+310T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661954 | ||||||
chr6:25661955
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+311T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661955 | ||||||
chr6:25662034
|
T | A | 1 | a0001c0001t0002g0233 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.246+390T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662034 | ||||||
chr6:25662104
|
G | C | 90 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(87): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.246+460G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662104 | ||||||
chr6:25662357
|
A | G | 1 | a0001c0001t0002g0233 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.246+713A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662357 | ||||||
chr6:25662458
|
G | A | 90 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(87): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.246+814G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662458 | ||||||
chr6:25662525
|
G | A | 3 | a0001c0001t0005g0263a0001c0001t0009g0262a0004c0005t0011g0264 | 3 | HG02486.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.246+881G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662525 | ||||||
chr6:25662560
|
T | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0237a0001c0001t0001g0238others(5): Show | 9 | HG01928.hp1 HG01943.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+916T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662560 | ||||||
chr6:25662562
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.246+918T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662562 | ||||||
chr6:25662575
|
T | C | 50 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0064others(47): Show | 53 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.246+931T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662575 | ||||||
chr6:25662645
|
A | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0237a0001c0001t0001g0238others(9): Show | 13 | HG00140.hp2 HG00280.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.246+1001A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662645 | ||||||
chr6:25662685
|
A | G | 4 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0228others(1): Show | 4 | HG01358.hp1 HG01496.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+1041A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662685 | ||||||
chr6:25662763
|
A | C | 1 | a0001c0001t0003g0043 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.246+1119A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662763 | ||||||
chr6:25662895
|
A | G | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.246+1251A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662895 | ||||||
chr6:25662997
|
C | T | 1 | a0001c0001t0004g0288 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.246+1353C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662997 | ||||||
chr6:25663034
|
C | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069 | 3 | HG02258.hp1 HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.246+1390C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663034 | ||||||
chr6:25663072
|
G | T | 1 | a0001c0001t0002g0142 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.246+1428G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663072 | ||||||
chr6:25663094
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.246+1450A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663094 | ||||||
chr6:25663123
|
G | A | 4 | a0001c0001t0001g0218a0001c0001t0002g0335a0001c0001t0003g0334others(1): Show | 4 | HG00621.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+1479G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663123 | ||||||
chr6:25663132
|
C | T | 28 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0033others(25): Show | 29 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.246+1488C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663132 | ||||||
chr6:25663280
|
A | G | 2 | a0001c0001t0003g0086a0001c0001t0016g0087 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.246+1636A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663280 | ||||||
chr6:25663291
|
T | C | 1 | a0001c0001t0004g0269 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.246+1647T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663291 | ||||||
chr6:25663296
|
A | G | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.247-1647A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663296 | ||||||
chr6:25663305
|
C | A | 1 | a0001c0001t0003g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.247-1638C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663305 | ||||||
chr6:25663343
|
C | A | 1 | a0001c0001t0002g0233 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.247-1600C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663343 | ||||||
chr6:25663382
|
T | G | 92 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(89): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.247-1561T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663382 | ||||||
chr6:25663675
|
A | G | 90 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(87): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.247-1268A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663675 | ||||||
chr6:25663920
|
T | G | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | HG01496.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.247-1023T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663920 | ||||||
chr6:25663957
|
T | C | 50 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0064others(47): Show | 53 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.247-986T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663957 | ||||||
chr6:25664028
|
A | T | 2 | a0001c0001t0002g0226a0001c0001t0010g0225 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.247-915A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25664028 | ||||||
chr6:25664451
|
C | T | 90 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(87): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.247-492C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25664451 | ||||||
chr6:25664753
|
T | A | 293 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(290): Show | 320 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.247-190T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25664753 | ||||||
chr6:25664813
|
C | T | 130 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0033others(127): Show | 142 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.247-130C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25664813 | ||||||
chr6:25664863
|
C | T | 3 | a0001c0001t0005g0263a0001c0001t0009g0262a0004c0005t0011g0264 | 3 | HG02486.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.247-80C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25664863 | ||||||
chr6:25665098
|
G | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0118 | 2 | HG02129.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.336+66G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665098 | ||||||
chr6:25665298
|
C | T | 1 | a0001c0001t0002g0005 | 2 | HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.336+266C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665298 | ||||||
chr6:25665334
|
A | G | 3 | a0001c0001t0005g0263a0001c0001t0009g0262a0004c0005t0011g0264 | 3 | HG02486.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.336+302A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665334 | ||||||
chr6:25665415
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.336+383C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665415 | ||||||
chr6:25665651
|
A | G | 2 | a0001c0001t0003g0086a0001c0001t0016g0087 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.336+619A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665651 | ||||||
chr6:25665682
|
C | A | 1 | a0001c0001t0005g0255 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.336+650C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665682 | ||||||
chr6:25665836
|
AT | A | 92 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(89): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.336+813delT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25665836 | |||||
chr6:25665936
|
G | A | 92 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(89): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.336+904G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665936 | ||||||
chr6:25665944
|
T | A | 5 | a0001c0001t0003g0205a0001c0001t0008g0017a0001c0001t0008g0161others(2): Show | 6 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.336+912T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665944 | ||||||
chr6:25665947
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.336+915T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665947 | ||||||
chr6:25666016
|
GTTAT | G | 337 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(334): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.336+1008_336+1011d others(6): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25666016 | |||||
chr6:25666033
|
T | A | 2 | a0001c0001t0001g0212a0001c0001t0002g0209 | 2 | NA18980.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.336+1001T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666033 | ||||||
chr6:25666177
|
TA | T | 93 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0033others(90): Show | 101 | HG00323.hp2 HG00408.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.336+1166delA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25666177 | |||||
chr6:25666177
|
TAA | T | 198 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(195): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.336+1165_336+1166d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25666177 | |||||
chr6:25666246
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.336+1214C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666246 | ||||||
chr6:25666285
|
G | A | 1 | a0008c0010t0003g0034 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.336+1253G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666285 | ||||||
chr6:25666304
|
T | C | 92 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(89): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.336+1272T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666304 | ||||||
chr6:25666456
|
T | G | 95 | a0001c0001t0001g0211a0001c0001t0001g0217a0001c0001t0002g0248others(92): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.336+1424T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666456 | ||||||
chr6:25666586
|
C | T | 48 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0064others(45): Show | 51 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.336+1554C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666586 | ||||||
chr6:25666782
|
A | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(106): Show | 121 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.336+1750A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666782 | ||||||
chr6:25666788
|
A | G | 1 | a0001c0001t0004g0265 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.336+1756A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666788 | ||||||
chr6:25666839
|
T | C | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.336+1807T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666839 | ||||||
chr6:25666916
|
C | T | 1 | a0001c0001t0002g0142 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.336+1884C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666916 | ||||||
chr6:25667000
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0155 | 2 | HG02155.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.336+1968C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667000 | ||||||
chr6:25667278
|
A | G | 1 | a0001c0001t0003g0140 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.337-2233A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667278 | ||||||
chr6:25667470
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.337-2041A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667470 | ||||||
chr6:25667557
|
C | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | NA19006.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.337-1954C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667557 | ||||||
chr6:25667639
|
G | A | 5 | a0001c0001t0003g0234a0003c0003t0003g0027a0003c0003t0003g0328others(2): Show | 6 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-1872G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667639 | ||||||
chr6:25667709
|
C | T | 6 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0008g0017others(3): Show | 7 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-1802C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667709 | ||||||
chr6:25667711
|
G | A | 183 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(180): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.337-1800G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667711 | ||||||
chr6:25667783
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.337-1728T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667783 | ||||||
chr6:25667802
|
C | T | 1 | a0004c0005t0004g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.337-1709C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667802 | ||||||
chr6:25667803
|
A | G | 17 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0002g0006others(14): Show | 19 | HG01175.hp2 HG01358.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.337-1708A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667803 | ||||||
chr6:25667836
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.337-1675T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667836 | ||||||
chr6:25667847
|
C | A | 90 | a0001c0001t0002g0259a0001c0001t0002g0331a0001c0001t0002g0333others(87): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.337-1664C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667847 | ||||||
chr6:25667898
|
A | G | 3 | a0001c0001t0004g0265a0001c0001t0006g0266a0001c0001t0006g0267 | 3 | HG02145.hp1 HG03130.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.337-1613A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667898 | ||||||
chr6:25667904
|
T | A | 1 | a0001c0001t0002g0333 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.337-1607T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667904 | ||||||
chr6:25667909
|
A | T | 3 | a0001c0001t0002g0331a0001c0001t0002g0333a0001c0001t0003g0332 | 3 | HG01106.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.337-1602A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667909 | ||||||
chr6:25667931
|
G | A | 6 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0008g0017others(3): Show | 7 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-1580G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667931 | ||||||
chr6:25667990
|
C | G | 6 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0008g0017others(3): Show | 7 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-1521C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667990 | ||||||
chr6:25668183
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.337-1328C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668183 | ||||||
chr6:25668217
|
GA | G | 179 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(176): Show | 194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1280delA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25668217 | |||||
chr6:25668378
|
C | T | 1 | a0001c0001t0002g0233 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.337-1133C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668378 | ||||||
chr6:25668396
|
C | T | 2 | a0001c0001t0005g0263a0001c0001t0009g0262 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.337-1115C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668396 | ||||||
chr6:25668452
|
A | T | 1 | a0001c0001t0002g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.337-1059A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668452 | ||||||
chr6:25668472
|
T | C | 31 | a0001c0001t0001g0019a0001c0001t0001g0211a0001c0001t0001g0212others(28): Show | 32 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.337-1039T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668472 | ||||||
chr6:25668693
|
G | A | 7 | a0001c0001t0002g0093a0001c0001t0013g0120a0002c0002t0003g0009others(4): Show | 8 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-818G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668693 | ||||||
chr6:25668700
|
A | AGATATAC others(12): Show |
3 | a0001c0001t0005g0263a0001c0001t0009g0262a0004c0005t0011g0264 | 3 | HG02486.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.337-809_337-808ins others(19): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25668700 | |||||
chr6:25668763
|
A | G | 3 | a0001c0001t0002g0058a0001c0001t0002g0065a0001c0001t0002g0066 | 3 | HG02630.hp1 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.337-748A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668763 | ||||||
chr6:25668929
|
G | A | 98 | a0001c0001t0002g0093a0001c0001t0002g0248a0001c0001t0002g0259others(95): Show | 108 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.337-582G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668929 | ||||||
chr6:25668955
|
C | T | 46 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0064others(43): Show | 49 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.337-556C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668955 | ||||||
chr6:25668966
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.337-545C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668966 | ||||||
chr6:25669050
|
G | T | 49 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0064others(46): Show | 52 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.337-461G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669050 | ||||||
chr6:25669077
|
G | C | 92 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0331others(89): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.337-434G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669077 | ||||||
chr6:25669110
|
C | CA | 157 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(154): Show | 173 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.337-385dupA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25669110 | |||||
chr6:25669110
|
C | CAA | 105 | a0001c0001t0001g0143a0001c0001t0001g0211a0001c0001t0001g0212others(102): Show | 114 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.337-386_337-385dup others(2): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25669110 | |||||
chr6:25669110
|
C | CAAA | 26 | a0001c0001t0001g0019a0001c0001t0001g0214a0001c0001t0001g0237others(23): Show | 28 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.337-387_337-385dup others(3): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25669110 | |||||
chr6:25669268
|
A | G | 101 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0002g0093others(98): Show | 112 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.337-243A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669268 | ||||||
chr6:25669297
|
G | A | 40 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0064others(37): Show | 43 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.337-214G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669297 | ||||||
chr6:25669408
|
A | T | 101 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0002g0093others(98): Show | 112 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.337-103A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669408 | ||||||
chr6:25669441
|
G | A | 41 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0064others(38): Show | 44 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.337-70G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669441 | ||||||
chr6:25669605
|
T | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0002g0093others(53): Show | 61 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.393+38T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 5/10 | chr6 | 25669605 | ||||||
chr6:25669797
|
T | A | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.394-202T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 5/10 | chr6 | 25669797 | ||||||
chr6:25670123
|
C | A | 17 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0002g0006others(14): Show | 19 | HG01175.hp2 HG01358.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.471+47C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670123 | ||||||
chr6:25670257
|
A | C | 1 | a0001c0001t0002g0036 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.471+181A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670257 | ||||||
chr6:25670303
|
G | A | 1 | a0001c0001t0006g0327 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.471+227G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670303 | ||||||
chr6:25670564
|
T | C | 91 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0002g0248others(88): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.471+488T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670564 | ||||||
chr6:25670597
|
C | T | 100 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(97): Show | 108 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.471+521C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670597 | ||||||
chr6:25670718
|
A | G | 36 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0004g0031others(33): Show | 40 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.471+642A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670718 | ||||||
chr6:25670805
|
C | G | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.471+729C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670805 | ||||||
chr6:25670995
|
C | G | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | HG01496.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.471+919C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670995 | ||||||
chr6:25671037
|
AAG | A | 45 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(42): Show | 51 | HG00408.hp1 HG00738.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.471+964_471+965del others(2): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 25671037 | |||||
chr6:25671171
|
T | A | 1 | a0001c0001t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.471+1095T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671171 | ||||||
chr6:25671252
|
A | G | 1 | a0001c0001t0003g0160 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.471+1176A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671252 | ||||||
chr6:25671398
|
CT | C | 90 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0002g0248others(87): Show | 100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.471+1323delT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671398 | ||||||
chr6:25671571
|
G | A | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.471+1495G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671571 | ||||||
chr6:25671618
|
A | T | 87 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0003g0230others(84): Show | 97 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.471+1542A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671618 | ||||||
chr6:25671645
|
C | T | 90 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0002g0248others(87): Show | 100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.471+1569C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671645 | ||||||
chr6:25671661
|
C | A | 2 | a0001c0001t0003g0229a0001c0001t0003g0231 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.471+1585C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671661 | ||||||
chr6:25671715
|
C | T | 1 | a0001c0001t0003g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.471+1639C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671715 | ||||||
chr6:25671716
|
C | T | 1 | a0001c0001t0003g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.471+1640C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671716 | ||||||
chr6:25672048
|
C | A | 2 | a0001c0001t0002g0226a0001c0001t0010g0225 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.471+1972C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672048 | ||||||
chr6:25672051
|
C | A | 1 | a0001c0001t0003g0334 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.471+1975C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672051 | ||||||
chr6:25672086
|
C | T | 8 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0002g0006others(5): Show | 10 | HG01175.hp2 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+2010C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672086 | ||||||
chr6:25672151
|
C | T | 2 | a0001c0001t0002g0007a0001c0001t0002g0061 | 3 | HG01515.hp1 HG01517.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.471+2075C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672151 | ||||||
chr6:25672333
|
A | G | 1 | a0001c0001t0004g0256 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.471+2257A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672333 | ||||||
chr6:25672583
|
G | A | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0217others(4): Show | 7 | HG00609.hp1 HG02135.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+2507G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672583 | ||||||
chr6:25672669
|
A | G | 50 | a0001c0001t0001g0113a0001c0001t0002g0248a0001c0001t0002g0259others(47): Show | 54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.471+2593A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672669 | ||||||
chr6:25672813
|
A | G | 1 | a0001c0001t0005g0278 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.471+2737A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672813 | ||||||
chr6:25673039
|
A | C | 296 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(293): Show | 323 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.471+2963A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673039 | ||||||
chr6:25673045
|
A | G | 23 | a0001c0001t0001g0019a0001c0001t0001g0211a0001c0001t0001g0212others(20): Show | 24 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.471+2969A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673045 | ||||||
chr6:25673052
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.471+2976T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673052 | ||||||
chr6:25673078
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.471+3002G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673078 | ||||||
chr6:25673136
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0063 | 3 | HG03239.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.471+3060T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673136 | ||||||
chr6:25673335
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.471+3259A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673335 | ||||||
chr6:25673398
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.471+3322C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673398 | ||||||
chr6:25673532
|
C | G | 1 | a0001c0001t0009g0262 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.471+3456C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673532 | ||||||
chr6:25673533
|
G | A | 21 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0002g0006others(18): Show | 24 | HG00642.hp2 HG01081.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.471+3457G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673533 | ||||||
chr6:25673579
|
T | C | 1 | a0001c0001t0004g0294 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.471+3503T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673579 | ||||||
chr6:25673736
|
G | A | 1 | a0001c0001t0009g0250 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.471+3660G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673736 | ||||||
chr6:25673860
|
G | T | 1 | a0001c0001t0003g0249 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.471+3784G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673860 | ||||||
chr6:25674017
|
A | C | 1 | a0001c0001t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.471+3941A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674017 | ||||||
chr6:25674281
|
A | G | 108 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(105): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.471+4205A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674281 | ||||||
chr6:25674315
|
C | A | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.471+4239C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674315 | ||||||
chr6:25674468
|
G | A | 337 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(334): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.471+4392G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674468 | ||||||
chr6:25674485
|
C | A | 1 | a0001c0001t0003g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.471+4409C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674485 | ||||||
chr6:25674497
|
T | C | 88 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(85): Show | 93 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.471+4421T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674497 | ||||||
chr6:25674507
|
G | A | 112 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 122 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.471+4431G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674507 | ||||||
chr6:25674668
|
C | T | 47 | a0001c0001t0001g0194a0001c0001t0002g0233a0001c0001t0004g0022others(44): Show | 53 | HG00408.hp1 HG00738.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.471+4592C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674668 | ||||||
chr6:25674691
|
A | G | 148 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0029others(145): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.471+4615A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674691 | ||||||
chr6:25674780
|
T | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0095a0001c0001t0001g0232others(9): Show | 13 | HG00280.hp2 HG00673.hp1 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.471+4704T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674780 | ||||||
chr6:25674806
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.471+4730T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674806 | ||||||
chr6:25675013
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.471+4937G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675013 | ||||||
chr6:25675049
|
G | T | 1 | a0001c0001t0001g0240 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.471+4973G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675049 | ||||||
chr6:25675140
|
C | T | 146 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0029others(143): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.471+5064C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675140 | ||||||
chr6:25675144
|
C | T | 2 | a0001c0001t0005g0309a0001c0001t0005g0310 | 2 | NA18943.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.471+5068C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675144 | ||||||
chr6:25675234
|
C | T | 2 | a0001c0001t0004g0277a0001c0001t0006g0285 | 2 | HG03831.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.471+5158C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675234 | ||||||
chr6:25675426
|
G | A | 2 | a0001c0001t0003g0086a0001c0001t0016g0087 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.471+5350G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675426 | ||||||
chr6:25675452
|
C | T | 3 | a0001c0001t0002g0248a0001c0001t0003g0249a0001c0001t0014g0219 | 3 | HG02559.hp2 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.471+5376C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675452 | ||||||
chr6:25675472
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.471+5396A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675472 | ||||||
chr6:25675536
|
T | G | 295 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(292): Show | 322 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.471+5460T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675536 | ||||||
chr6:25675607
|
G | A | 1 | a0001c0001t0002g0007 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.471+5531G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675607 | ||||||
chr6:25675626
|
C | T | 112 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 122 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.471+5550C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675626 | ||||||
chr6:25675775
|
C | G | 1 | a0009c0011t0003g0336 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.471+5699C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675775 | ||||||
chr6:25675886
|
T | C | 295 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(292): Show | 322 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.471+5810T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675886 | ||||||
chr6:25676045
|
C | G | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.472-5906C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676045 | ||||||
chr6:25676169
|
G | A | 259 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(256): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.472-5782G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676169 | ||||||
chr6:25676301
|
C | T | 1 | a0001c0001t0004g0294 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.472-5650C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676301 | ||||||
chr6:25676307
|
C | T | 1 | a0001c0001t0014g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.472-5644C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676307 | ||||||
chr6:25676512
|
T | C | 295 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(292): Show | 322 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.472-5439T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676512 | ||||||
chr6:25676542
|
A | C | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0217others(4): Show | 7 | HG00609.hp1 HG02135.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-5409A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676542 | ||||||
chr6:25676587
|
G | A | 146 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0029others(143): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.472-5364G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676587 | ||||||
chr6:25676669
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.472-5282T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676669 | ||||||
chr6:25676741
|
A | C | 30 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0002g0006others(27): Show | 34 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.472-5210A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676741 | ||||||
chr6:25676768
|
TTTCCATC others(5): Show |
T | 108 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(105): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.472-5168_472-5157d others(14): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 25676768 | |||||
chr6:25676819
|
G | A | 1 | a0001c0001t0005g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.472-5132G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676819 | ||||||
chr6:25676980
|
C | G | 1 | a0001c0001t0008g0057 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.472-4971C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676980 | ||||||
chr6:25677087
|
G | A | 295 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(292): Show | 322 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.472-4864G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677087 | ||||||
chr6:25677108
|
C | G | 33 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0002g0006others(30): Show | 37 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.472-4843C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677108 | ||||||
chr6:25677320
|
T | C | 1 | a0001c0001t0014g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.472-4631T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677320 | ||||||
chr6:25677339
|
G | T | 1 | a0001c0001t0008g0017 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.472-4612G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677339 | ||||||
chr6:25677378
|
G | A | 1 | a0001c0001t0014g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.472-4573G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677378 | ||||||
chr6:25677559
|
A | T | 1 | a0001c0001t0003g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.472-4392A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677559 | ||||||
chr6:25677660
|
A | G | 1 | a0001c0001t0004g0276 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.472-4291A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677660 | ||||||
chr6:25677705
|
A | G | 113 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 123 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.472-4246A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677705 | ||||||
chr6:25677726
|
A | C | 147 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0029others(144): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.472-4225A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677726 | ||||||
chr6:25677826
|
A | G | 1 | a0001c0001t0004g0308 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.472-4125A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677826 | ||||||
chr6:25677945
|
A | C | 1 | a0001c0001t0002g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.472-4006A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677945 | ||||||
chr6:25678011
|
T | C | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0217others(4): Show | 7 | HG00609.hp1 HG02135.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-3940T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678011 | ||||||
chr6:25678450
|
C | T | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 121 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.472-3501C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678450 | ||||||
chr6:25678657
|
C | T | 1 | a0001c0001t0010g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.472-3294C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678657 | ||||||
chr6:25678680
|
G | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18973.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.472-3271G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678680 | ||||||
chr6:25678683
|
A | T | 16 | a0001c0001t0002g0001a0001c0001t0002g0067a0001c0001t0002g0068others(13): Show | 18 | HG01243.hp1 HG01891.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.472-3268A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678683 | ||||||
chr6:25678799
|
C | T | 1 | a0001c0001t0003g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.472-3152C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678799 | ||||||
chr6:25678804
|
G | T | 1 | a0001c0001t0002g0259 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.472-3147G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678804 | ||||||
chr6:25678815
|
C | T | 1 | a0001c0001t0005g0286 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.472-3136C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678815 | ||||||
chr6:25678816
|
A | G | 295 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(292): Show | 322 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.472-3135A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678816 | ||||||
chr6:25678868
|
C | T | 2 | a0001c0001t0005g0263a0001c0001t0009g0262 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.472-3083C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678868 | ||||||
chr6:25678951
|
A | C | 1 | a0001c0001t0003g0032 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.472-3000A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678951 | ||||||
chr6:25679142
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.472-2809G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679142 | ||||||
chr6:25679171
|
G | A | 1 | a0001c0001t0014g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.472-2780G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679171 | ||||||
chr6:25679430
|
A | G | 30 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0002g0006others(27): Show | 34 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.472-2521A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679430 | ||||||
chr6:25679483
|
GGT | G | 109 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.472-2456_472-2455d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 25679483 | |||||
chr6:25679560
|
TC | T | 3 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0001t0003g0176 | 3 | HG00099.hp2 HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.472-2390delC | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679560 | ||||||
chr6:25679732
|
A | G | 121 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(118): Show | 132 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.472-2219A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679732 | ||||||
chr6:25679899
|
AAAT | A | 103 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(100): Show | 112 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.472-2051_472-2049d others(5): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679899 | ||||||
chr6:25679927
|
T | C | 1 | a0001c0001t0002g0209 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.472-2024T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679927 | ||||||
chr6:25679955
|
G | C | 1 | a0001c0001t0002g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.472-1996G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679955 | ||||||
chr6:25679974
|
A | G | 2 | a0001c0001t0002g0168a0001c0001t0002g0169 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.472-1977A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679974 | ||||||
chr6:25680045
|
CAA | C | 109 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.472-1904_472-1903d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 25680045 | |||||
chr6:25680103
|
A | C | 312 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(309): Show | 341 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.472-1848A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680103 | ||||||
chr6:25680182
|
A | C | 5 | a0001c0001t0003g0234a0003c0003t0003g0027a0003c0003t0003g0328others(2): Show | 6 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-1769A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680182 | ||||||
chr6:25680221
|
CATAATGT others(4): Show |
C | 1 | a0001c0001t0006g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.472-1727_472-1717d others(13): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 25680221 | |||||
chr6:25680295
|
T | C | 1 | a0001c0001t0002g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.472-1656T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680295 | ||||||
chr6:25680301
|
T | C | 1 | a0009c0011t0003g0336 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.472-1650T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680301 | ||||||
chr6:25680538
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0121 | 2 | NA18978.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.472-1413T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680538 | ||||||
chr6:25680556
|
C | A | 1 | a0001c0001t0003g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.472-1395C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680556 | ||||||
chr6:25680573
|
C | T | 1 | a0004c0005t0011g0264 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.472-1378C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680573 | ||||||
chr6:25680913
|
C | T | 108 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(105): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.472-1038C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680913 | ||||||
chr6:25680939
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.472-1012A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680939 | ||||||
chr6:25681027
|
G | A | 3 | a0001c0001t0005g0021a0001c0001t0005g0295a0001c0001t0005g0315 | 4 | HG00738.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-924G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681027 | ||||||
chr6:25681255
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.472-696T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681255 | ||||||
chr6:25681263
|
C | A | 1 | a0001c0001t0002g0150 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.472-688C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681263 | ||||||
chr6:25681462
|
G | A | 1 | a0001c0001t0005g0278 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.472-489G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681462 | ||||||
chr6:25681525
|
G | A | 108 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(105): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.472-426G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681525 | ||||||
chr6:25681816
|
T | G | 1 | a0001c0001t0004g0282 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.472-135T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681816 | ||||||
chr6:25681835
|
C | T | 1 | a0001c0001t0004g0024 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.472-116C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681835 | ||||||
chr6:25682034
|
A | C | 106 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(103): Show | 116 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.527+28A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682034 | ||||||
chr6:25682213
|
G | A | 5 | a0001c0001t0003g0230a0001c0001t0004g0265a0001c0001t0006g0266others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+207G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682213 | ||||||
chr6:25682350
|
G | A | 3 | a0001c0001t0002g0335a0001c0001t0003g0334a0009c0011t0003g0336 | 3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.527+344G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682350 | ||||||
chr6:25682386
|
C | CA | 295 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(292): Show | 322 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.527+380_527+381ins others(1): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682386 | ||||||
chr6:25682397
|
G | GCACTTCA others(4): Show |
5 | a0001c0001t0003g0230a0001c0001t0004g0265a0001c0001t0006g0266others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+395_527+396ins others(11): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25682397 | |||||
chr6:25682415
|
G | C | 1 | a0003c0003t0003g0328 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.527+409G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682415 | ||||||
chr6:25682482
|
G | A | 1 | a0004c0005t0004g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.527+476G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682482 | ||||||
chr6:25682506
|
A | C | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.527+500A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682506 | ||||||
chr6:25682507
|
A | T | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.527+501A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682507 | ||||||
chr6:25682537
|
C | T | 2 | a0001c0001t0002g0248a0001c0001t0003g0249 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.527+531C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682537 | ||||||
chr6:25682701
|
C | G | 112 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0030others(109): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.527+695C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682701 | ||||||
chr6:25683052
|
A | C | 291 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(288): Show | 318 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.527+1046A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683052 | ||||||
chr6:25683097
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.527+1091C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683097 | ||||||
chr6:25683142
|
G | T | 4 | a0001c0001t0002g0226a0001c0001t0005g0263a0001c0001t0009g0262others(1): Show | 4 | HG02109.hp2 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.527+1136G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683142 | ||||||
chr6:25683164
|
A | C | 1 | a0001c0001t0004g0258 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.527+1158A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683164 | ||||||
chr6:25683185
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0177 | 2 | NA18970.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.527+1179C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683185 | ||||||
chr6:25683186
|
G | A | 5 | a0001c0001t0003g0230a0001c0001t0004g0265a0001c0001t0006g0266others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+1180G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683186 | ||||||
chr6:25683200
|
C | T | 5 | a0001c0001t0003g0230a0001c0001t0004g0265a0001c0001t0006g0266others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+1194C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683200 | ||||||
chr6:25683300
|
G | A | 1 | a0001c0001t0003g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.527+1294G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683300 | ||||||
chr6:25683338
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.527+1332G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683338 | ||||||
chr6:25683412
|
C | A | 3 | a0001c0001t0003g0089a0001c0001t0003g0099a0001c0001t0003g0119 | 3 | HG01934.hp2 HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.527+1406C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683412 | ||||||
chr6:25683446
|
G | C | 2 | a0001c0001t0004g0288a0001c0001t0005g0020 | 3 | HG00609.hp2 HG00673.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.527+1440G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683446 | ||||||
chr6:25683539
|
T | C | 2 | a0001c0001t0001g0215a0001c0001t0002g0210 | 2 | NA18975.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.527+1533T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683539 | ||||||
chr6:25683630
|
G | GT | 38 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0059others(35): Show | 41 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.527+1625dupT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25683630 | |||||
chr6:25683716
|
G | C | 1 | a0001c0001t0003g0178 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.527+1710G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683716 | ||||||
chr6:25683726
|
C | T | 89 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(86): Show | 96 | HG00621.hp1 HG01074.hp2 HG01081.hp1 others(93): Show |
intron_variant | MODIFIER | c.527+1720C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683726 | ||||||
chr6:25683727
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.527+1721G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683727 | ||||||
chr6:25683922
|
G | T | 15 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0002g0056others(12): Show | 16 | HG01106.hp2 HG01358.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.527+1916G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683922 | ||||||
chr6:25684051
|
A | G | 188 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0029others(185): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.527+2045A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684051 | ||||||
chr6:25684054
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0121 | 2 | NA18978.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.527+2048C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684054 | ||||||
chr6:25684081
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.527+2075C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684081 | ||||||
chr6:25684140
|
C | A | 1 | a0001c0001t0001g0240 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.527+2134C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684140 | ||||||
chr6:25684177
|
T | C | 181 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0029others(178): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.527+2171T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684177 | ||||||
chr6:25684328
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.527+2322A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684328 | ||||||
chr6:25684356
|
C | T | 1 | a0001c0001t0004g0284 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.527+2350C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684356 | ||||||
chr6:25684378
|
C | T | 6 | a0001c0001t0003g0002a0001c0001t0003g0178a0001c0001t0003g0179others(3): Show | 8 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.527+2372C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684378 | ||||||
chr6:25684425
|
G | T | 164 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(161): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.527+2419G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684425 | ||||||
chr6:25684507
|
G | A | 13 | a0001c0001t0002g0001a0001c0001t0002g0058a0001c0001t0002g0065others(10): Show | 15 | HG02630.hp1 HG02717.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.527+2501G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684507 | ||||||
chr6:25684527
|
G | T | 6 | a0001c0001t0001g0217a0001c0001t0002g0208a0001c0001t0002g0209others(3): Show | 6 | HG02135.hp1 NA18940.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.527+2521G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684527 | ||||||
chr6:25684542
|
C | T | 3 | a0001c0001t0002g0036a0001c0001t0005g0021a0001c0001t0005g0278 | 4 | HG01168.hp2 HG01169.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.527+2536C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684542 | ||||||
chr6:25684574
|
C | A | 7 | a0001c0001t0001g0053a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.527+2568C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684574 | ||||||
chr6:25684708
|
G | A | 16 | a0001c0001t0002g0001a0001c0001t0002g0056a0001c0001t0002g0071others(13): Show | 18 | HG01358.hp1 HG01993.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.527+2702G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684708 | ||||||
chr6:25684725
|
G | A | 167 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.527+2719G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684725 | ||||||
chr6:25684844
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.527+2838A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684844 | ||||||
chr6:25684922
|
CAATAGAC others(5): Show |
C | 3 | a0001c0001t0008g0057a0001c0001t0009g0250a0001c0001t0009g0262 | 3 | HG02895.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.527+2923_527+2934d others(14): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25684922 | |||||
chr6:25684925
|
T | C | 2 | a0001c0001t0003g0032a0001c0001t0003g0249 | 2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.527+2919T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684925 | ||||||
chr6:25685019
|
A | G | 83 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(80): Show | 87 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.527+3013A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685019 | ||||||
chr6:25685026
|
C | T | 1 | a0001c0001t0002g0054 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.527+3020C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685026 | ||||||
chr6:25685083
|
T | C | 5 | a0001c0001t0003g0074a0001c0001t0003g0076a0001c0001t0003g0230others(2): Show | 5 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+3077T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685083 | ||||||
chr6:25685132
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.527+3126G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685132 | ||||||
chr6:25685134
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.527+3128G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685134 | ||||||
chr6:25685172
|
A | G | 7 | a0001c0001t0008g0017a0001c0001t0008g0057a0001c0001t0008g0161others(4): Show | 8 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.527+3166A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685172 | ||||||
chr6:25685236
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.527+3230G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685236 | ||||||
chr6:25685261
|
G | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0138others(6): Show | 10 | HG00438.hp2 HG01496.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.527+3255G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685261 | ||||||
chr6:25685264
|
G | C | 169 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(166): Show | 180 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.527+3258G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685264 | ||||||
chr6:25685488
|
A | G | 13 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(10): Show | 13 | HG02055.hp2 HG02080.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.527+3482A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685488 | ||||||
chr6:25685529
|
G | A | 18 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(15): Show | 18 | HG02055.hp2 HG02080.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.527+3523G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685529 | ||||||
chr6:25685635
|
C | G | 1 | a0001c0001t0016g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.528-3537C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685635 | ||||||
chr6:25685650
|
G | GTATAAT | 6 | a0001c0001t0003g0002a0001c0001t0003g0178a0001c0001t0003g0179others(3): Show | 8 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.528-3505_528-3500d others(8): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25685650 | |||||
chr6:25685650
|
GTATAATT others(5): Show |
G | 1 | a0001c0001t0002g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.528-3511_528-3500d others(14): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25685650 | |||||
chr6:25685661
|
A | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(143): Show | 154 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.528-3511A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685661 | ||||||
chr6:25685805
|
G | T | 85 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0138others(82): Show | 96 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.528-3367G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685805 | ||||||
chr6:25686153
|
T | G | 1 | a0001c0001t0004g0304 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.528-3019T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686153 | ||||||
chr6:25686177
|
C | T | 152 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(149): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.528-2995C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686177 | ||||||
chr6:25686586
|
T | G | 1 | a0001c0001t0005g0292 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.528-2586T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686586 | ||||||
chr6:25686602
|
TTATCAGA others(9): Show |
T | 1 | a0001c0001t0005g0274 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.528-2569_528-2554d others(18): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686602 | ||||||
chr6:25686614
|
T | C | 1 | a0001c0001t0004g0269 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.528-2558T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686614 | ||||||
chr6:25686752
|
A | G | 3 | a0001c0001t0001g0237a0001c0001t0004g0279a0001c0001t0004g0281 | 3 | NA18964.hp1 NA18986.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.528-2420A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686752 | ||||||
chr6:25686865
|
T | C | 3 | a0001c0001t0008g0057a0001c0001t0009g0250a0001c0001t0009g0262 | 3 | HG02895.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.528-2307T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686865 | ||||||
chr6:25686959
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG01261.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.528-2213C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686959 | ||||||
chr6:25687351
|
T | C | 147 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(144): Show | 155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.528-1821T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687351 | ||||||
chr6:25687397
|
C | A | 4 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0028others(1): Show | 7 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.528-1775C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687397 | ||||||
chr6:25687525
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.528-1647A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687525 | ||||||
chr6:25687579
|
T | C | 1 | a0001c0004t0001g0127 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.528-1593T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687579 | ||||||
chr6:25687667
|
T | C | 147 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(144): Show | 155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.528-1505T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687667 | ||||||
chr6:25687759
|
T | A | 6 | a0001c0001t0002g0001a0001c0001t0002g0071a0001c0001t0002g0072others(3): Show | 8 | NA18945.hp2 NA18955.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.528-1413T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687759 | ||||||
chr6:25687818
|
T | C | 5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0213others(2): Show | 5 | NA18940.hp2 NA19003.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.528-1354T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687818 | ||||||
chr6:25687850
|
AT | A | 23 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0138others(20): Show | 25 | HG00438.hp2 HG01496.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.528-1314delT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25687850 | |||||
chr6:25688456
|
A | C | 1 | a0002c0002t0003g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.528-716A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25688456 | ||||||
chr6:25688577
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.528-595G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25688577 | ||||||
chr6:25688687
|
A | C | 1 | a0001c0001t0003g0178 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.528-485A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25688687 | ||||||
chr6:25688801
|
C | CAA | 8 | a0001c0001t0004g0320a0001c0001t0008g0017a0001c0001t0008g0057others(5): Show | 9 | HG00642.hp2 HG01081.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.528-358_528-357dup others(2): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25688801 | |||||
chr6:25688801
|
C | CAAAAAAA others(3): Show |
11 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0054others(8): Show | 12 | HG00741.hp2 HG01515.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.528-366_528-357dup others(10): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25688801 | |||||
chr6:25688801
|
C | CAAAAAAA others(4): Show |
14 | a0001c0001t0001g0045a0001c0001t0001g0095a0001c0001t0001g0164others(11): Show | 16 | HG00323.hp2 HG01069.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.528-367_528-357dup others(11): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25688801 | |||||
chr6:25688801
|
C | CAAAAAAA others(5): Show |
111 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.528-368_528-357dup others(12): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25688801 | |||||
chr6:25688801
|
C | CAAAAAAA others(6): Show |
19 | a0001c0001t0001g0039a0001c0001t0001g0105a0001c0001t0001g0107others(16): Show | 19 | HG00438.hp1 HG00544.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.528-369_528-357dup others(13): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25688801 | |||||
chr6:25688942
|
T | G | 1 | a0005c0007t0002g0207 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.528-230T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25688942 | ||||||
chr6:25688996
|
C | T | 5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0213others(2): Show | 5 | NA18940.hp2 NA19003.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.528-176C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25688996 | ||||||
chr6:25689145
|
C | T | 6 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0075others(3): Show | 6 | HG01496.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.528-27C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25689145 | ||||||
chr6:25689150
|
AT | A | 275 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(272): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.528-9delT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25689150 | |||||
chr6:25689228
|
A | T | 10 | a0001c0001t0002g0056a0001c0001t0002g0093a0001c0001t0002g0226others(7): Show | 10 | HG01358.hp1 HG01993.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.573+11A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 8/10 | chr6 | 25689228 | ||||||
chr6:25689259
|
G | C | 169 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(166): Show | 180 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.573+42G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 8/10 | chr6 | 25689259 | ||||||
chr6:25689361
|
G | T | 5 | a0001c0001t0002g0096a0001c0001t0002g0142a0001c0001t0002g0150others(2): Show | 5 | NA18956.hp1 NA18983.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-112G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 8/10 | chr6 | 25689361 | ||||||
chr6:25689563
|
A | G | 1 | a0001c0001t0003g0249 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.633+31A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25689563 | ||||||
chr6:25689630
|
A | G | 2 | a0001c0001t0003g0032a0001c0001t0003g0249 | 2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.633+98A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25689630 | ||||||
chr6:25689933
|
A | G | 1 | a0001c0001t0002g0096 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.633+401A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25689933 | ||||||
chr6:25690062
|
G | A | 85 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0138others(82): Show | 96 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.633+530G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690062 | ||||||
chr6:25690118
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.633+586T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690118 | ||||||
chr6:25690172
|
C | T | 1 | a0001c0001t0003g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.633+640C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690172 | ||||||
chr6:25690175
|
G | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG01069.hp1 HG01515.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.633+643G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690175 | ||||||
chr6:25690223
|
A | G | 7 | a0001c0001t0008g0017a0001c0001t0008g0057a0001c0001t0008g0161others(4): Show | 8 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.633+691A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690223 | ||||||
chr6:25690708
|
C | A | 51 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0015others(48): Show | 60 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.634-348C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690708 | ||||||
chr6:25690912
|
T | C | 1 | a0001c0001t0004g0272 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.634-144T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690912 | ||||||
chr6:25690949
|
A | G | 5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0213others(2): Show | 5 | NA18940.hp2 NA19003.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-107A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690949 | ||||||
chr6:25691134
|
C | T | 17 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0051others(14): Show | 18 | HG00741.hp2 HG01433.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.702+10C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691134 | ||||||
chr6:25691596
|
G | A | 1 | a0001c0001t0003g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.702+472G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691596 | ||||||
chr6:25691637
|
T | G | 1 | a0001c0001t0001g0156 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.702+513T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691637 | ||||||
chr6:25691669
|
C | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0249 | 2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+545C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691669 | ||||||
chr6:25691670
|
G | A | 51 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0015others(48): Show | 60 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.702+546G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691670 | ||||||
chr6:25691688
|
A | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0249 | 2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+564A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691688 | ||||||
chr6:25691728
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.702+604A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691728 | ||||||
chr6:25691793
|
T | C | 22 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0138others(19): Show | 24 | HG00438.hp2 HG01496.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.702+669T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691793 | ||||||
chr6:25691923
|
C | A | 17 | a0001c0001t0002g0001a0001c0001t0002g0056a0001c0001t0002g0071others(14): Show | 19 | HG01358.hp1 HG01993.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.702+799C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691923 | ||||||
chr6:25692012
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.702+888T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25692012 | ||||||
chr6:25692685
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.702+1561G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25692685 | ||||||
chr6:25692909
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.702+1785G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25692909 | ||||||
chr6:25692966
|
G | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0134a0001c0001t0001g0214 | 4 | NA18965.hp1 NA18987.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+1842G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25692966 | ||||||
chr6:25693046
|
C | T | 39 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0010others(36): Show | 45 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.702+1922C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693046 | ||||||
chr6:25693173
|
C | T | 5 | a0002c0002t0003g0009a0002c0002t0003g0094a0002c0002t0003g0115others(2): Show | 6 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+2049C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693173 | ||||||
chr6:25693177
|
C | T | 2 | a0001c0001t0002g0175a0001c0001t0005g0305 | 2 | HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.702+2053C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693177 | ||||||
chr6:25693180
|
G | T | 1 | a0001c0001t0005g0322 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.702+2056G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693180 | ||||||
chr6:25693204
|
C | T | 5 | a0001c0001t0002g0096a0001c0001t0002g0142a0001c0001t0002g0150others(2): Show | 5 | NA18956.hp1 NA18983.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+2080C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693204 | ||||||
chr6:25693265
|
C | T | 7 | a0001c0001t0002g0001a0001c0001t0002g0071a0001c0001t0002g0072others(4): Show | 9 | NA18945.hp2 NA18955.hp2 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+2141C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693265 | ||||||
chr6:25693287
|
T | A | 1 | a0001c0001t0001g0148 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.702+2163T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693287 | ||||||
chr6:25693353
|
T | G | 168 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0138others(165): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.702+2229T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693353 | ||||||
chr6:25693437
|
G | A | 1 | a0001c0001t0003g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.702+2313G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693437 | ||||||
chr6:25693447
|
G | A | 168 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0138others(165): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.702+2323G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693447 | ||||||
chr6:25693451
|
C | CA | 84 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0041others(81): Show | 92 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.702+2352dupA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25693451 | |||||
chr6:25693451
|
C | CAA | 22 | a0001c0001t0001g0040a0001c0001t0001g0131a0001c0001t0002g0007others(19): Show | 23 | HG01192.hp2 HG01433.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.702+2351_702+2352d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25693451 | |||||
chr6:25693451
|
CA | C | 22 | a0001c0001t0001g0045a0001c0001t0001g0105a0001c0001t0002g0073others(19): Show | 23 | HG00323.hp1 HG00323.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.702+2352delA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25693451 | |||||
chr6:25693593
|
T | G | 1 | a0001c0001t0005g0314 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.702+2469T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693593 | ||||||
chr6:25693656
|
GATT | G | 147 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(144): Show | 155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.702+2535_702+2537d others(5): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25693656 | |||||
chr6:25693674
|
TTAAC | T | 17 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0051others(14): Show | 18 | HG00741.hp2 HG01433.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.702+2555_702+2558d others(6): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25693674 | |||||
chr6:25693878
|
C | T | 2 | a0001c0001t0002g0201a0001c0001t0002g0248 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.702+2754C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693878 | ||||||
chr6:25693898
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.702+2774A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693898 | ||||||
chr6:25694080
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.702+2956C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694080 | ||||||
chr6:25694130
|
C | T | 4 | a0001c0001t0008g0017a0001c0001t0008g0161a0001c0001t0008g0162others(1): Show | 5 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+3006C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694130 | ||||||
chr6:25694200
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.702+3076C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694200 | ||||||
chr6:25694263
|
T | G | 48 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0010others(45): Show | 54 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.702+3139T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694263 | ||||||
chr6:25694456
|
T | C | 50 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0030others(47): Show | 52 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.702+3332T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694456 | ||||||
chr6:25694574
|
A | G | 17 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0051others(14): Show | 18 | HG00741.hp2 HG01433.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.702+3450A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694574 | ||||||
chr6:25694776
|
C | T | 9 | a0001c0001t0003g0074a0001c0001t0003g0076a0001c0001t0003g0086others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+3652C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694776 | ||||||
chr6:25694999
|
G | A | 1 | a0001c0001t0003g0032 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.702+3875G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694999 | ||||||
chr6:25695065
|
T | G | 1 | a0001c0001t0003g0146 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.702+3941T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695065 | ||||||
chr6:25695130
|
C | T | 8 | a0001c0001t0002g0093a0001c0001t0002g0226a0001c0001t0002g0228others(5): Show | 8 | HG01358.hp1 HG01993.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+4006C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695130 | ||||||
chr6:25695213
|
G | T | 140 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(137): Show | 147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.702+4089G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695213 | ||||||
chr6:25695238
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.702+4114T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695238 | ||||||
chr6:25695317
|
T | C | 332 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.702+4193T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695317 | ||||||
chr6:25695592
|
T | C | 170 | a0001c0001t0001g0019a0001c0001t0001g0088a0001c0001t0001g0125others(167): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.702+4468T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695592 | ||||||
chr6:25695963
|
T | C | 17 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0051others(14): Show | 18 | HG00741.hp2 HG01433.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.702+4839T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695963 | ||||||
chr6:25696151
|
A | T | 1 | a0001c0001t0004g0258 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.702+5027A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25696151 | ||||||
chr6:25696383
|
T | A | 169 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0138others(166): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.703-4824T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25696383 | ||||||
chr6:25696750
|
A | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18973.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.703-4457A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25696750 | ||||||
chr6:25697136
|
A | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0118a0001c0001t0001g0167others(1): Show | 4 | HG02083.hp1 HG02129.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-4071A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697136 | ||||||
chr6:25697175
|
C | T | 1 | a0001c0001t0005g0255 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.703-4032C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697175 | ||||||
chr6:25697316
|
G | T | 5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0213others(2): Show | 5 | NA18940.hp2 NA19003.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-3891G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697316 | ||||||
chr6:25697348
|
C | G | 332 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.703-3859C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697348 | ||||||
chr6:25697400
|
A | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0018a0001c0001t0003g0235 | 6 | HG02486.hp1 HG02615.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-3807A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697400 | ||||||
chr6:25697933
|
C | T | 1 | a0001c0001t0005g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703-3274C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697933 | ||||||
chr6:25698232
|
A | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0337 | 3 | HG02165.hp2 NA18943.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.703-2975A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698232 | ||||||
chr6:25698253
|
C | T | 139 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(136): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.703-2954C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698253 | ||||||
chr6:25698566
|
A | T | 9 | a0001c0001t0003g0074a0001c0001t0003g0076a0001c0001t0003g0086others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.703-2641A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698566 | ||||||
chr6:25698585
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0132 | 2 | NA19068.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.703-2622C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698585 | ||||||
chr6:25698765
|
A | G | 1 | a0001c0006t0003g0046 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.703-2442A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698765 | ||||||
chr6:25698878
|
G | A | 5 | a0002c0002t0003g0009a0002c0002t0003g0094a0002c0002t0003g0115others(2): Show | 6 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-2329G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698878 | ||||||
chr6:25698895
|
C | T | 11 | a0001c0001t0002g0056a0001c0001t0002g0163a0001c0001t0002g0175others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.703-2312C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698895 | ||||||
chr6:25698991
|
G | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0222 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.703-2216G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698991 | ||||||
chr6:25699055
|
C | A | 47 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0010others(44): Show | 53 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.703-2152C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699055 | ||||||
chr6:25699088
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.703-2119G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699088 | ||||||
chr6:25699122
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG01168.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.703-2085G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699122 | ||||||
chr6:25699170
|
G | A | 1 | a0001c0001t0003g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.703-2037G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699170 | ||||||
chr6:25699245
|
A | G | 5 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0075others(2): Show | 5 | HG01496.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-1962A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699245 | ||||||
chr6:25699422
|
C | G | 1 | a0001c0001t0002g0259 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.703-1785C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699422 | ||||||
chr6:25699446
|
C | T | 1 | a0001c0001t0003g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.703-1761C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699446 | ||||||
chr6:25699589
|
C | CA | 15 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0030others(12): Show | 16 | HG00438.hp2 HG00673.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-1597dupA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25699589 | |||||
chr6:25699589
|
C | CAA | 13 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0213others(10): Show | 13 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.703-1598_703-1597d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25699589 | |||||
chr6:25699589
|
CA | C | 20 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0132others(17): Show | 22 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.703-1597delA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25699589 | |||||
chr6:25699607
|
A | G | 1 | a0001c0001t0005g0260 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.703-1600A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699607 | ||||||
chr6:25699635
|
A | G | 1 | a0001c0004t0001g0103 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.703-1572A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699635 | ||||||
chr6:25699691
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.703-1516A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699691 | ||||||
chr6:25699754
|
C | T | 2 | a0002c0002t0003g0009a0002c0002t0003g0117 | 3 | HG02572.hp2 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.703-1453C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699754 | ||||||
chr6:25699771
|
A | G | 139 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(136): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.703-1436A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699771 | ||||||
chr6:25699782
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.703-1425G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699782 | ||||||
chr6:25700021
|
G | A | 1 | a0002c0002t0003g0115 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.703-1186G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700021 | ||||||
chr6:25700055
|
G | A | 1 | a0001c0001t0003g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.703-1152G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700055 | ||||||
chr6:25700079
|
C | G | 1 | a0001c0001t0007g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.703-1128C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700079 | ||||||
chr6:25700090
|
C | G | 5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0213others(2): Show | 5 | NA18940.hp2 NA19003.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-1117C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700090 | ||||||
chr6:25700114
|
G | A | 13 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0018others(10): Show | 18 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.703-1093G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700114 | ||||||
chr6:25700122
|
G | A | 88 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(85): Show | 93 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.703-1085G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700122 | ||||||
chr6:25700180
|
A | G | 169 | a0001c0001t0001g0019a0001c0001t0001g0125a0001c0001t0001g0138others(166): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.703-1027A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700180 | ||||||
chr6:25700224
|
C | T | 2 | a0001c0001t0003g0229a0001c0001t0003g0231 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.703-983C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700224 | ||||||
chr6:25700241
|
C | A | 1 | a0001c0001t0013g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.703-966C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700241 | ||||||
chr6:25700241
|
C | CA | 8 | a0001c0001t0001g0109a0001c0001t0001g0154a0001c0001t0001g0245others(5): Show | 8 | HG01081.hp1 HG01243.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-945dupA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25700241 | |||||
chr6:25700241
|
C | CAA | 188 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(185): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.703-946_703-945dup others(2): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25700241 | |||||
chr6:25700241
|
C | CAAA | 118 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0040others(115): Show | 130 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.703-947_703-945dup others(3): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25700241 | |||||
chr6:25700241
|
C | CAAAA | 15 | a0001c0001t0001g0138a0001c0001t0001g0212a0001c0001t0001g0240others(12): Show | 15 | HG00741.hp1 HG02145.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.703-948_703-945dup others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25700241 | |||||
chr6:25700241
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0249 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.703-960_703-945dup others(16): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25700241 | |||||
chr6:25700611
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.703-596T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700611 |