geneid | 54823 |
---|---|
ensemblid | ENSG00000116668.13 |
hgncid | 16785 |
symbol | SWT1 |
name | SWT1 RNA endoribonuclease homolog |
refseq_nuc | NM_017673.7 |
refseq_prot | NP_060143.4 |
ensembl_nuc | ENST00000367500.9 |
ensembl_prot | ENSP00000356470.4 |
mane_status | MANE Select |
chr | chr1 |
start | 185157167 |
end | 185291781 |
strand | + |
ver | v1.2 |
region | chr1:185157167-185291781 |
region5000 | chr1:185152167-185296781 |
regionname0 | SWT1_chr1_185157167_185291781 |
regionname5000 | SWT1_chr1_185152167_185296781 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 900 | 122 | 11 | 28 | 65 | 6 | 10 | 45 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0002 | 0/0 | 900 | 72 | 16 | 19 | 25 | 4 | 8 | 22 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003 | 0/0 | 900 | 68 | 42 | 7 | 17 | 1 | 1 | 11 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0004 | 0/0 | 900 | 27 | 7 | 10 | 5 | 1 | 4 | 5 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0005 | 0/0 | 900 | 10 | 0 | 0 | 10 | 0 | 0 | 10 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0006 | 0/0 | 900 | 9 | 6 | 0 | 3 | 0 | 0 | 3 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0007 | 0/0 | 900 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0008 | 0/0 | 900 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0009 | 0/0 | 900 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0010 | 0/0 | 900 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0011 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0012 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0013 | 0/0 | 900 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0014 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0015 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0016 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2703 | 117 | 10 | 26 | 63 | 6 | 10 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0002 | 0/0 | 2703 | 44 | 13 | 10 | 14 | 4 | 3 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0003 | 0/0 | 2703 | 41 | 16 | 6 | 17 | 1 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0004 | 0/0 | 2703 | 28 | 3 | 9 | 11 | 0 | 5 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0005 | 0/0 | 2703 | 26 | 25 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0006 | 0/0 | 2703 | 21 | 7 | 8 | 4 | 0 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0007 | 0/0 | 2703 | 10 | 0 | 0 | 10 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0008 | 0/0 | 2703 | 7 | 6 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0009 | 0/0 | 2703 | 6 | 0 | 2 | 1 | 1 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0010 | 0/0 | 2703 | 5 | 5 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0011 | 0/0 | 2703 | 4 | 1 | 2 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0012 | 0/0 | 2703 | 3 | 3 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0013 | 0/0 | 2703 | 2 | 0 | 0 | 2 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0014 | 0/0 | 2703 | 2 | 0 | 0 | 2 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0015 | 0/0 | 2703 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0016 | 0/0 | 2703 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0017 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0018 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0019 | 0/0 | 2703 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0020 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0021 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0022 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0023 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
c0024 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1136 | 272 | 60 | 67 | 109 | 12 | 22 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
t0002 | 0/0 | 1136 | 20 | 0 | 0 | 18 | 0 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
t0003 | 0/0 | 1136 | 15 | 15 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
t0004 | 0/0 | 1136 | 12 | 12 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
t0005 | 0/0 | 1136 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
t0006 | 0/0 | 1136 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
t0007 | 0/0 | 1136 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
t0008 | 0/0 | 1136 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
t0009 | 0/0 | 1136 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
t0010 | 0/0 | 1136 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
t0011 | 0/0 | 1136 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2703 | 117 | 10 | 26 | 63 | 6 | 10 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0001c0011 | 0/0 | 2703 | 4 | 1 | 2 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0001c0019 | 0/0 | 2703 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0002c0002 | 0/0 | 2703 | 44 | 13 | 10 | 14 | 4 | 3 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0002c0004 | 0/0 | 2703 | 28 | 3 | 9 | 11 | 0 | 5 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003c0003 | 0/0 | 2703 | 41 | 16 | 6 | 17 | 1 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003c0005 | 0/0 | 2703 | 26 | 25 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003c0021 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0004c0006 | 0/0 | 2703 | 21 | 7 | 8 | 4 | 0 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0004c0009 | 0/0 | 2703 | 6 | 0 | 2 | 1 | 1 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0005c0007 | 0/0 | 2703 | 10 | 0 | 0 | 10 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0006c0008 | 0/0 | 2703 | 7 | 6 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0006c0014 | 0/0 | 2703 | 2 | 0 | 0 | 2 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0007c0010 | 0/0 | 2703 | 5 | 5 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0008c0012 | 0/0 | 2703 | 3 | 3 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0009c0017 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0009c0023 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0010c0013 | 0/0 | 2703 | 2 | 0 | 0 | 2 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0011c0020 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0012c0018 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0013c0016 | 0/0 | 2703 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0014c0015 | 0/0 | 2703 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0015c0022 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0016c0024 | 0/0 | 2703 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3838 | 93 | 8 | 25 | 44 | 6 | 8 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0001c0001t0002 | 0/0 | 3838 | 20 | 0 | 0 | 18 | 0 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0001c0001t0004 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0001c0001t0005 | 0/0 | 3838 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0001c0001t0006 | 0/0 | 3838 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0001c0001t0007 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0001c0011t0001 | 0/0 | 3838 | 3 | 0 | 2 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0001c0011t0008 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0001c0019t0001 | 0/0 | 3838 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0002c0002t0001 | 0/0 | 3838 | 44 | 13 | 10 | 14 | 4 | 3 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0002c0004t0001 | 0/0 | 3838 | 28 | 3 | 9 | 11 | 0 | 5 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003c0003t0001 | 0/0 | 3838 | 39 | 14 | 6 | 17 | 1 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003c0003t0004 | 0/0 | 3838 | 2 | 2 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003c0005t0001 | 0/0 | 3838 | 3 | 2 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003c0005t0003 | 0/0 | 3838 | 13 | 13 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003c0005t0004 | 0/0 | 3838 | 9 | 9 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003c0005t0009 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0003c0021t0011 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0004c0006t0001 | 0/0 | 3838 | 21 | 7 | 8 | 4 | 0 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0004c0009t0001 | 0/0 | 3838 | 6 | 0 | 2 | 1 | 1 | 2 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0005c0007t0001 | 0/0 | 3838 | 10 | 0 | 0 | 10 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0006c0008t0001 | 0/0 | 3838 | 5 | 4 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0006c0008t0003 | 0/0 | 3838 | 2 | 2 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0006c0014t0001 | 0/0 | 3838 | 2 | 0 | 0 | 2 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0007c0010t0001 | 0/0 | 3838 | 4 | 4 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0007c0010t0010 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0008c0012t0001 | 0/0 | 3838 | 3 | 3 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0009c0017t0001 | 0/0 | 3838 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0009c0023t0001 | 0/0 | 3838 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0010c0013t0001 | 0/0 | 3838 | 2 | 0 | 0 | 2 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0011c0020t0001 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0012c0018t0001 | 0/0 | 3838 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0013c0016t0001 | 0/0 | 3838 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0014c0015t0001 | 0/0 | 3838 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0015c0022t0001 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
a0016c0024t0001 | 0/0 | 3838 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | copy fasta | chr1 | 185152167 | 185296781 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0011t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0011t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0011t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0011t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0001c0019t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0002c0004t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0003t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0005t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0003c0021t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0006t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0004c0009t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0005c0007t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0008t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0014t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0006c0014t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0010t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0010t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0010t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0010t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0007c0010t0010g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0008c0012t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0008c0012t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0008c0012t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0009c0017t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0009c0023t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0010c0013t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0010c0013t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0011c0020t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0012c0018t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0013c0016t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0014c0015t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0015c0022t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
a0016c0024t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00280 | hp2 | a0004 | c0009 | t0001 | g0061 | EUR | FIN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0198 | EUR | FIN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0185 | EUR | FIN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0194 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0209 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00558 | hp2 | a0003 | c0003 | t0001 | g0220 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00609 | hp2 | a0003 | c0003 | t0001 | g0203 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00621 | hp2 | a0014 | c0015 | t0001 | g0090 | EAS | CHS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00639 | hp2 | a0004 | c0009 | t0001 | g0130 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00738 | hp2 | a0004 | c0006 | t0001 | g0144 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0288 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01069 | hp2 | a0012 | c0018 | t0001 | g0029 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01070 | hp1 | a0004 | c0009 | t0001 | g0068 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01070 | hp2 | a0001 | c0011 | t0001 | g0161 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0287 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0178 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01081 | hp1 | a0004 | c0006 | t0001 | g0165 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0100 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0240 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01106 | hp1 | a0003 | c0003 | t0001 | g0211 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01167 | hp2 | a0002 | c0004 | t0001 | g0300 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01168 | hp1 | a0001 | c0011 | t0001 | g0158 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01168 | hp2 | a0009 | c0017 | t0001 | g0076 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01169 | hp1 | a0002 | c0004 | t0001 | g0301 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01169 | hp2 | a0009 | c0023 | t0001 | g0162 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01192 | hp1 | a0003 | c0003 | t0001 | g0204 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01192 | hp2 | a0004 | c0006 | t0001 | g0163 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01243 | hp1 | a0003 | c0005 | t0001 | g0231 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01255 | hp1 | a0002 | c0004 | t0001 | g0309 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01257 | hp1 | a0003 | c0003 | t0001 | g0205 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01257 | hp2 | a0004 | c0006 | t0001 | g0166 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01346 | hp1 | a0004 | c0006 | t0001 | g0143 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01496 | hp1 | a0002 | c0004 | t0001 | g0289 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0152 | EUR | IBS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01884 | hp1 | a0011 | c0020 | t0001 | g0131 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01884 | hp2 | a0015 | c0022 | t0001 | g0009 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01891 | hp1 | a0006 | c0008 | t0001 | g0140 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01891 | hp2 | a0003 | c0005 | t0004 | g0008 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01928 | hp1 | a0004 | c0006 | t0001 | g0223 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01928 | hp2 | a0002 | c0004 | t0001 | g0303 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01943 | hp1 | a0004 | c0006 | t0001 | g0145 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01943 | hp2 | a0002 | c0004 | t0001 | g0312 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01952 | hp1 | a0002 | c0004 | t0001 | g0304 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01975 | hp1 | a0002 | c0004 | t0001 | g0294 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0206 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01981 | hp1 | a0002 | c0004 | t0001 | g0322 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02040 | hp1 | a0001 | c0019 | t0001 | g0047 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02040 | hp2 | a0002 | c0004 | t0001 | g0315 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02055 | hp1 | a0001 | c0011 | t0008 | g0261 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02055 | hp2 | a0003 | c0005 | t0003 | g0249 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02080 | hp1 | a0003 | c0003 | t0001 | g0208 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | KHV | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02145 | hp2 | a0008 | c0012 | t0001 | g0021 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02148 | hp1 | a0016 | c0024 | t0001 | g0176 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02148 | hp2 | a0004 | c0006 | t0001 | g0159 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02165 | hp1 | a0003 | c0003 | t0001 | g0201 | EAS | CDX | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0263 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0239 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02280 | hp2 | a0006 | c0008 | t0001 | g0141 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0197 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02451 | hp1 | a0003 | c0005 | t0003 | g0254 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02572 | hp1 | a0007 | c0010 | t0001 | g0229 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0216 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02622 | hp1 | a0003 | c0003 | t0001 | g0235 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02622 | hp2 | a0006 | c0008 | t0003 | g0244 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02630 | hp1 | a0004 | c0006 | t0001 | g0226 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0256 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02647 | hp1 | a0003 | c0005 | t0004 | g0269 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02647 | hp2 | a0004 | c0006 | t0001 | g0227 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02717 | hp1 | a0003 | c0005 | t0004 | g0266 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02717 | hp2 | a0006 | c0008 | t0003 | g0245 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02723 | hp2 | a0003 | c0005 | t0003 | g0248 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0212 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02809 | hp2 | a0003 | c0003 | t0004 | g0233 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02818 | hp1 | a0003 | c0005 | t0003 | g0253 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02818 | hp2 | a0007 | c0010 | t0001 | g0071 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02886 | hp1 | a0004 | c0006 | t0001 | g0225 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02886 | hp2 | a0003 | c0005 | t0004 | g0007 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02895 | hp1 | a0008 | c0012 | t0001 | g0020 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0272 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02896 | hp2 | a0003 | c0005 | t0003 | g0247 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02897 | hp1 | a0003 | c0005 | t0003 | g0003 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02897 | hp2 | a0003 | c0003 | t0001 | g0271 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02922 | hp1 | a0003 | c0005 | t0004 | g0270 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02965 | hp1 | a0003 | c0003 | t0001 | g0241 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02965 | hp2 | a0003 | c0003 | t0001 | g0264 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02970 | hp1 | a0003 | c0005 | t0001 | g0014 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0257 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02976 | hp2 | a0003 | c0005 | t0004 | g0230 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03041 | hp1 | a0003 | c0021 | t0011 | g0132 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0236 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03098 | hp2 | a0003 | c0003 | t0004 | g0234 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03130 | hp1 | a0004 | c0006 | t0001 | g0160 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03130 | hp2 | a0003 | c0005 | t0001 | g0232 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03139 | hp1 | a0003 | c0003 | t0001 | g0237 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03139 | hp2 | a0003 | c0005 | t0003 | g0228 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03195 | hp1 | a0006 | c0008 | t0001 | g0142 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03195 | hp2 | a0003 | c0003 | t0001 | g0238 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03209 | hp1 | a0003 | c0005 | t0004 | g0268 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03209 | hp2 | a0007 | c0010 | t0010 | g0085 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03225 | hp1 | a0003 | c0005 | t0003 | g0003 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03225 | hp2 | a0004 | c0006 | t0001 | g0167 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0214 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03453 | hp1 | a0003 | c0005 | t0004 | g0265 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03453 | hp2 | a0007 | c0010 | t0001 | g0073 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0273 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03490 | hp1 | a0004 | c0009 | t0001 | g0113 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03490 | hp2 | a0004 | c0006 | t0001 | g0153 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03491 | hp2 | a0002 | c0004 | t0001 | g0027 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03492 | hp1 | a0004 | c0009 | t0001 | g0114 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03492 | hp2 | a0002 | c0004 | t0001 | g0028 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03516 | hp1 | a0003 | c0005 | t0003 | g0246 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | ESN | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0260 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03540 | hp2 | a0003 | c0005 | t0003 | g0255 | AFR | GWD | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03579 | hp1 | a0003 | c0005 | t0004 | g0267 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03654 | hp2 | a0004 | c0006 | t0001 | g0164 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0179 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03688 | hp1 | a0002 | c0004 | t0001 | g0015 | SAS | STU | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03688 | hp2 | a0002 | c0004 | t0001 | g0297 | SAS | STU | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03704 | hp1 | a0013 | c0016 | t0001 | g0018 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0187 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03927 | hp1 | a0003 | c0003 | t0001 | g0190 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG04228 | hp2 | a0002 | c0004 | t0001 | g0308 | SAS | STU | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18522 | hp1 | a0003 | c0005 | t0003 | g0252 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0213 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18612 | hp1 | a0002 | c0004 | t0001 | g0311 | EAS | CHB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0215 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18906 | hp2 | a0003 | c0005 | t0003 | g0250 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18939 | hp2 | a0004 | c0006 | t0001 | g0150 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18941 | hp1 | a0005 | c0007 | t0001 | g0296 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18942 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18943 | hp1 | a0003 | c0003 | t0001 | g0196 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18946 | hp2 | a0003 | c0003 | t0001 | g0202 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18948 | hp1 | a0006 | c0014 | t0001 | g0293 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18949 | hp1 | a0003 | c0003 | t0001 | g0193 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18950 | hp1 | a0002 | c0004 | t0001 | g0087 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18951 | hp2 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18954 | hp1 | a0002 | c0004 | t0001 | g0314 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18961 | hp1 | a0003 | c0003 | t0001 | g0200 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18967 | hp1 | a0002 | c0004 | t0001 | g0321 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18969 | hp1 | a0006 | c0008 | t0001 | g0189 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18970 | hp1 | a0005 | c0007 | t0001 | g0307 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18973 | hp2 | a0004 | c0006 | t0001 | g0148 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18977 | hp1 | a0010 | c0013 | t0001 | g0074 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0195 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18983 | hp1 | a0002 | c0004 | t0001 | g0320 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18983 | hp2 | a0004 | c0006 | t0001 | g0146 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18989 | hp1 | a0005 | c0007 | t0001 | g0323 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18989 | hp2 | a0006 | c0014 | t0001 | g0295 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18992 | hp1 | a0003 | c0003 | t0001 | g0207 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18992 | hp2 | a0005 | c0007 | t0001 | g0299 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18999 | hp1 | a0003 | c0003 | t0001 | g0210 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19000 | hp1 | a0005 | c0007 | t0001 | g0305 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19000 | hp2 | a0003 | c0003 | t0001 | g0222 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19002 | hp1 | a0004 | c0006 | t0001 | g0147 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19006 | hp1 | a0002 | c0004 | t0001 | g0318 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19009 | hp1 | a0005 | c0007 | t0001 | g0242 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19011 | hp2 | a0010 | c0013 | t0001 | g0075 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19030 | hp1 | a0008 | c0012 | t0001 | g0019 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19030 | hp2 | a0003 | c0003 | t0001 | g0155 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19043 | hp1 | a0002 | c0004 | t0001 | g0292 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19043 | hp2 | a0003 | c0005 | t0003 | g0251 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19056 | hp1 | a0005 | c0007 | t0001 | g0243 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19057 | hp2 | a0005 | c0007 | t0001 | g0298 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19066 | hp1 | a0002 | c0004 | t0001 | g0317 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19068 | hp1 | a0004 | c0009 | t0001 | g0081 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19068 | hp2 | a0001 | c0011 | t0001 | g0149 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19072 | hp2 | a0005 | c0007 | t0001 | g0313 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19074 | hp1 | a0002 | c0004 | t0001 | g0319 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0192 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19081 | hp2 | a0005 | c0007 | t0001 | g0306 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19090 | hp1 | a0002 | c0004 | t0001 | g0302 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19091 | hp2 | a0002 | c0004 | t0001 | g0316 | EAS | JPT | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA19240 | hp2 | a0004 | c0006 | t0001 | g0224 | AFR | YRI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0157 | EUR | TSI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0183 | EUR | TSI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02109 | hp2 | a0003 | c0005 | t0009 | g0004 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0156 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG02559 | hp2 | a0006 | c0008 | t0001 | g0139 | AFR | ACB | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG06807 | hp1 | a0002 | c0004 | t0001 | g0010 | AFR | USA | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20300 | hp1 | a0002 | c0004 | t0001 | g0310 | AFR | USA | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA20300 | hp2 | a0007 | c0010 | t0001 | g0072 | AFR | USA | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
NA21309 | hp2 | a0004 | c0006 | t0001 | g0262 | AFR | LWK | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0119 | REF | REF | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | SWT1_chr1_185152167_185296781 | SWT1 | chr1 | 185152167 | 185296781 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:185174589
|
A | G | 6 | a0002a0003a0005others(3): Show | 161 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(158): Show |
missense_variant | MODERATE | c.442A>G | p.Ile148Val | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/19 | 599/3838 | 442/2703 | 148/900 | chr1 | 185174589 | ||
chr1:185174607
|
C | A | 1 | a0016 | 1 | HG02148.hp1 | missense_variant | MODERATE | c.460C>A | p.Pro154Thr | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/19 | 617/3838 | 460/2703 | 154/900 | chr1 | 185174607 | ||
chr1:185174692
|
A | G | 1 | a0007 | 5 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(2): Show |
missense_variant | MODERATE | c.545A>G | p.Lys182Arg | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/19 | 702/3838 | 545/2703 | 182/900 | chr1 | 185174692 | ||
chr1:185174693
|
G | T | 1 | a0008 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.546G>T | p.Lys182Asn | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/19 | 703/3838 | 546/2703 | 182/900 | chr1 | 185174693 | ||
chr1:185184329
|
A | G | 1 | a0011 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1225A>G | p.Thr409Ala | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 8/19 | 1382/3838 | 1225/2703 | 409/900 | chr1 | 185184329 | ||
chr1:185202737
|
A | G | 5 | a0002a0005a0006others(2): Show | 94 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(91): Show |
missense_variant | MODERATE | c.1607A>G | p.His536Arg | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/19 | 1764/3838 | 1607/2703 | 536/900 | chr1 | 185202737 | ||
chr1:185204702
|
A | G | 1 | a0012 | 1 | HG01069.hp2 | missense_variant&splice_region_variant | MODERATE | c.1672A>G | p.Thr558Ala | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/19 | 1829/3838 | 1672/2703 | 558/900 | chr1 | 185204702 | ||
chr1:185204724
|
A | G | 1 | a0009 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.1694A>G | p.Tyr565Cys | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/19 | 1851/3838 | 1694/2703 | 565/900 | chr1 | 185204724 | ||
chr1:185206667
|
C | G | 1 | a0013 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.1876C>G | p.Gln626Glu | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/19 | 2033/3838 | 1876/2703 | 626/900 | chr1 | 185206667 | ||
chr1:185206705
|
A | C | 1 | a0005 | 10 | NA18941.hp1 NA18970.hp1 NA18989.hp1 others(7): Show |
missense_variant | MODERATE | c.1914A>C | p.Leu638Phe | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/19 | 2071/3838 | 1914/2703 | 638/900 | chr1 | 185206705 | ||
chr1:185221934
|
A | C | 1 | a0014 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.2207A>C | p.Gln736Pro | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/19 | 2364/3838 | 2207/2703 | 736/900 | chr1 | 185221934 | ||
chr1:185271342
|
A | G | 7 | a0002a0004a0005others(4): Show | 115 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(112): Show |
missense_variant | MODERATE | c.2461A>G | p.Asn821Asp | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/19 | 2618/3838 | 2461/2703 | 821/900 | chr1 | 185271342 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:185166613
|
A | G | 7 | a0001c0011a0002c0002a0003c0003others(4): Show | 119 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(116): Show |
synonymous_variant | LOW | c.126A>G | p.Ser42Ser | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/19 | 283/3838 | 126/2703 | 42/900 | chr1 | 185166613 | ||
chr1:185174627
|
G | A | 2 | a0003c0021a0015c0022 | 2 | HG01884.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.480G>A | p.Val160Val | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/19 | 637/3838 | 480/2703 | 160/900 | chr1 | 185174627 | ||
chr1:185202738
|
C | T | 1 | a0001c0019 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.1608C>T | p.His536His | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/19 | 1765/3838 | 1608/2703 | 536/900 | chr1 | 185202738 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:185290819
|
T | G | 1 | a0001c0001t0005 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 16 | chr1 | 185290819 | |||||
chr1:185290873
|
A | G | 1 | a0003c0021t0011 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 70 | chr1 | 185290873 | |||||
chr1:185290939
|
A | G | 1 | a0001c0001t0002 | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*136A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 136 | chr1 | 185290939 | |||||
chr1:185290974
|
A | C | 1 | a0007c0010t0010 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 171 | chr1 | 185290974 | |||||
chr1:185291071
|
G | C | 1 | a0001c0001t0006 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*268G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 268 | chr1 | 185291071 | |||||
chr1:185291229
|
C | T | 1 | a0003c0005t0009 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 426 | chr1 | 185291229 | |||||
chr1:185291283
|
T | G | 2 | a0003c0005t0003a0006c0008t0003 | 15 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*480T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 480 | chr1 | 185291283 | |||||
chr1:185291331
|
C | T | 3 | a0001c0001t0004a0003c0003t0004a0003c0005t0004 | 12 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*528C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 528 | chr1 | 185291331 | |||||
chr1:185291383
|
T | A | 3 | a0001c0001t0007a0003c0005t0009a0003c0021t0011 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*580T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 580 | chr1 | 185291383 | |||||
chr1:185291536
|
A | C | 1 | a0001c0011t0008 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*733A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 19/19 | 733 | chr1 | 185291536 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:185157511
|
G | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10+197G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185157511 | ||||||
chr1:185157564
|
GC | G | 322 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(319): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-10+253delC | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 185157564 | |||||
chr1:185157690
|
A | G | 1 | a0005c0007t0001g0323 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-10+376A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185157690 | ||||||
chr1:185157734
|
G | T | 35 | a0001c0001t0002g0290a0001c0001t0002g0291a0002c0004t0001g0289others(32): Show | 35 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.-10+420G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185157734 | ||||||
chr1:185158093
|
G | A | 4 | a0001c0001t0001g0006a0003c0005t0004g0007a0003c0005t0004g0008others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+779G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158093 | ||||||
chr1:185158223
|
G | A | 1 | a0002c0004t0001g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10+909G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158223 | ||||||
chr1:185158259
|
A | G | 2 | a0002c0002t0001g0287a0002c0002t0001g0288 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-10+945A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158259 | ||||||
chr1:185158261
|
C | T | 13 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(10): Show | 13 | HG02071.hp2 HG03654.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+947C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158261 | ||||||
chr1:185158361
|
G | T | 1 | a0002c0002t0001g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10+1047G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158361 | ||||||
chr1:185158383
|
C | T | 10 | a0003c0003t0001g0263a0003c0003t0001g0264a0003c0003t0001g0271others(7): Show | 10 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+1069C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158383 | ||||||
chr1:185158417
|
C | CA | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013 | 3 | NA18972.hp1 NA19006.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-10+1105dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 185158417 | |||||
chr1:185158509
|
C | CT | 52 | a0001c0001t0002g0290a0001c0001t0002g0291a0001c0011t0008g0261others(49): Show | 53 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(50): Show |
intron_variant | MODIFIER | c.-10+1209dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 185158509 | |||||
chr1:185158684
|
A | G | 2 | a0006c0008t0003g0244a0006c0008t0003g0245 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-10+1370A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158684 | ||||||
chr1:185158979
|
T | C | 15 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(12): Show | 15 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+1665T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185158979 | ||||||
chr1:185159118
|
C | T | 134 | a0001c0011t0001g0149a0001c0011t0001g0158a0001c0011t0001g0161others(131): Show | 135 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-9-1715C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159118 | ||||||
chr1:185159158
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-9-1675C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159158 | ||||||
chr1:185159173
|
G | A | 1 | a0003c0005t0001g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-9-1660G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159173 | ||||||
chr1:185159327
|
T | A | 1 | a0002c0004t0001g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9-1506T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159327 | ||||||
chr1:185159359
|
G | A | 2 | a0002c0002t0001g0136a0002c0002t0001g0137 | 2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-9-1474G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159359 | ||||||
chr1:185159413
|
C | G | 47 | a0002c0004t0001g0010a0002c0004t0001g0289a0002c0004t0001g0292others(44): Show | 48 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.-9-1420C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159413 | ||||||
chr1:185159475
|
A | G | 12 | a0003c0003t0001g0235a0003c0003t0001g0236a0003c0003t0001g0237others(9): Show | 12 | HG01099.hp2 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-1358A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159475 | ||||||
chr1:185159549
|
C | A | 5 | a0002c0002t0001g0138a0006c0008t0001g0139a0006c0008t0001g0140others(2): Show | 5 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1284C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159549 | ||||||
chr1:185159696
|
C | CAT | 3 | a0004c0006t0001g0143a0004c0006t0001g0144a0004c0006t0001g0145 | 3 | HG00738.hp2 HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-9-1128_-9-1127dup others(2): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 185159696 | |||||
chr1:185159755
|
C | T | 5 | a0003c0003t0001g0237a0003c0003t0001g0238a0003c0003t0001g0239others(2): Show | 5 | HG01099.hp2 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1078C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159755 | ||||||
chr1:185159809
|
C | G | 47 | a0002c0004t0001g0010a0002c0004t0001g0289a0002c0004t0001g0292others(44): Show | 48 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.-9-1024C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185159809 | ||||||
chr1:185160028
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-9-805A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185160028 | ||||||
chr1:185160513
|
C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-9-320C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185160513 | ||||||
chr1:185160631
|
G | C | 118 | a0001c0011t0001g0149a0001c0011t0001g0158a0001c0011t0001g0161others(115): Show | 119 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-9-202G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185160631 | ||||||
chr1:185160757
|
A | G | 5 | a0001c0001t0001g0133a0004c0006t0001g0224a0004c0006t0001g0225others(2): Show | 5 | HG02630.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-76A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 1/18 | chr1 | 185160757 | ||||||
chr1:185160944
|
T | C | 1 | a0003c0005t0001g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.84+19T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185160944 | ||||||
chr1:185160993
|
C | G | 2 | a0003c0021t0011g0132a0015c0022t0001g0009 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.84+68C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185160993 | ||||||
chr1:185161221
|
T | TA | 5 | a0001c0011t0001g0149a0004c0006t0001g0146a0004c0006t0001g0147others(2): Show | 5 | NA18939.hp2 NA18973.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+299dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 185161221 | |||||
chr1:185161274
|
C | G | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.84+349C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185161274 | ||||||
chr1:185161285
|
A | G | 12 | a0003c0003t0001g0235a0003c0003t0001g0236a0003c0003t0001g0237others(9): Show | 12 | HG01099.hp2 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.84+360A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185161285 | ||||||
chr1:185161627
|
G | A | 1 | a0002c0002t0001g0151 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.84+702G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185161627 | ||||||
chr1:185161716
|
A | G | 1 | a0004c0006t0001g0150 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.84+791A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185161716 | ||||||
chr1:185162288
|
A | C | 1 | a0004c0009t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.84+1363A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162288 | ||||||
chr1:185162361
|
C | T | 34 | a0002c0004t0001g0289a0002c0004t0001g0294a0002c0004t0001g0297others(31): Show | 34 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.84+1436C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162361 | ||||||
chr1:185162417
|
A | G | 1 | a0001c0011t0008g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.84+1492A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162417 | ||||||
chr1:185162707
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.84+1782G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162707 | ||||||
chr1:185162730
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84+1805C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162730 | ||||||
chr1:185162742
|
T | C | 1 | a0002c0002t0001g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.84+1817T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162742 | ||||||
chr1:185162811
|
A | G | 1 | a0004c0006t0001g0223 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.84+1886A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185162811 | ||||||
chr1:185163037
|
C | T | 13 | a0003c0005t0001g0231a0003c0005t0001g0232a0003c0005t0004g0007others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+2112C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163037 | ||||||
chr1:185163153
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.84+2228T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163153 | ||||||
chr1:185163214
|
A | G | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(15): Show |
intron_variant | MODIFIER | c.84+2289A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163214 | ||||||
chr1:185163393
|
C | CT | 11 | a0001c0001t0001g0006a0001c0001t0001g0125a0001c0001t0001g0127others(8): Show | 11 | HG00597.hp2 HG00741.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+2486dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 185163393 | |||||
chr1:185163393
|
CT | C | 7 | a0002c0002t0001g0154a0002c0004t0001g0294a0004c0006t0001g0153others(4): Show | 7 | HG01975.hp1 HG02896.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+2486delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 185163393 | |||||
chr1:185163432
|
C | T | 2 | a0003c0003t0001g0271a0003c0003t0001g0272 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.84+2507C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163432 | ||||||
chr1:185163487
|
G | A | 34 | a0002c0004t0001g0289a0002c0004t0001g0294a0002c0004t0001g0297others(31): Show | 34 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.84+2562G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163487 | ||||||
chr1:185163708
|
A | G | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(15): Show |
intron_variant | MODIFIER | c.84+2783A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163708 | ||||||
chr1:185163710
|
T | C | 203 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(200): Show | 205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.84+2785T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163710 | ||||||
chr1:185163723
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.84+2798A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163723 | ||||||
chr1:185163899
|
A | G | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | NA18973.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.85-2673A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185163899 | ||||||
chr1:185164328
|
T | G | 2 | a0003c0003t0001g0155a0003c0003t0001g0156 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.85-2244T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185164328 | ||||||
chr1:185164663
|
G | A | 2 | a0003c0005t0001g0014a0003c0005t0003g0228 | 2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.85-1909G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185164663 | ||||||
chr1:185164753
|
A | C | 2 | a0008c0012t0001g0020a0008c0012t0001g0021 | 2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.85-1819A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185164753 | ||||||
chr1:185164892
|
A | C | 38 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0089others(35): Show | 38 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.85-1680A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185164892 | ||||||
chr1:185165133
|
G | A | 3 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247 | 4 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-1439G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165133 | ||||||
chr1:185165337
|
A | G | 1 | a0003c0003t0001g0220 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.85-1235A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165337 | ||||||
chr1:185165374
|
C | T | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.85-1198C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165374 | ||||||
chr1:185165464
|
T | C | 1 | a0003c0003t0001g0220 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.85-1108T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165464 | ||||||
chr1:185165535
|
C | T | 2 | a0003c0021t0011g0132a0015c0022t0001g0009 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.85-1037C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165535 | ||||||
chr1:185165739
|
C | T | 3 | a0002c0002t0001g0217a0002c0002t0001g0218a0002c0002t0001g0219 | 3 | NA18961.hp2 NA19083.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.85-833C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165739 | ||||||
chr1:185165800
|
G | A | 1 | a0002c0004t0001g0297 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.85-772G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165800 | ||||||
chr1:185165920
|
C | T | 1 | a0002c0004t0001g0087 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.85-652C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185165920 | ||||||
chr1:185166121
|
C | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85-451C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185166121 | ||||||
chr1:185166309
|
A | G | 9 | a0003c0005t0004g0007a0003c0005t0004g0008a0003c0005t0004g0230others(6): Show | 9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-263A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185166309 | ||||||
chr1:185166436
|
C | G | 1 | a0013c0016t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.85-136C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 2/18 | chr1 | 185166436 | ||||||
chr1:185166916
|
A | T | 1 | a0002c0002t0001g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+264A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185166916 | ||||||
chr1:185166918
|
T | A | 52 | a0001c0001t0001g0006a0001c0001t0001g0022a0002c0004t0001g0010others(49): Show | 53 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.165+266T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185166918 | ||||||
chr1:185167167
|
C | T | 47 | a0002c0004t0001g0010a0002c0004t0001g0289a0002c0004t0001g0292others(44): Show | 48 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.165+515C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167167 | ||||||
chr1:185167226
|
A | G | 9 | a0003c0005t0004g0007a0003c0005t0004g0008a0003c0005t0004g0230others(6): Show | 9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+574A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167226 | ||||||
chr1:185167232
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.165+580A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167232 | ||||||
chr1:185167326
|
C | A | 184 | a0001c0011t0001g0149a0001c0011t0001g0158a0001c0011t0001g0161others(181): Show | 186 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.165+674C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167326 | ||||||
chr1:185167366
|
G | A | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.165+714G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167366 | ||||||
chr1:185167417
|
T | C | 9 | a0003c0005t0004g0007a0003c0005t0004g0008a0003c0005t0004g0230others(6): Show | 9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+765T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167417 | ||||||
chr1:185167695
|
C | A | 1 | a0002c0002t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.166-645C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167695 | ||||||
chr1:185167872
|
T | G | 1 | a0002c0002t0001g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.166-468T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185167872 | ||||||
chr1:185168234
|
G | A | 1 | a0001c0011t0008g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-106G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185168234 | ||||||
chr1:185168322
|
T | TAAATGAT others(4): Show |
203 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(200): Show | 205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.166-18_166-17insAA others(9): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185168322 | ||||||
chr1:185168329
|
A | T | 203 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(200): Show | 205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.166-11A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | chr1 | 185168329 | ||||||
chr1:185168332
|
T | TAA | 203 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(200): Show | 205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
splice_region_variant&intron_variant | LOW | c.166-7_166-6insAA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 185168332 | |||||
chr1:185168453
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.224+55A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168453 | ||||||
chr1:185168496
|
C | T | 203 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(200): Show | 205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.224+98C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168496 | ||||||
chr1:185168541
|
G | A | 2 | a0003c0005t0004g0265a0003c0005t0004g0266 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.224+143G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168541 | ||||||
chr1:185168889
|
A | G | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(15): Show |
intron_variant | MODIFIER | c.224+491A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168889 | ||||||
chr1:185168937
|
C | T | 2 | a0002c0002t0001g0215a0002c0002t0001g0216 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.224+539C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168937 | ||||||
chr1:185168973
|
C | T | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.224+575C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185168973 | ||||||
chr1:185169003
|
T | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG00438.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.224+605T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169003 | ||||||
chr1:185169194
|
G | T | 1 | a0002c0002t0001g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.224+796G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169194 | ||||||
chr1:185169196
|
A | C | 2 | a0002c0004t0001g0010a0002c0004t0001g0292 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.224+798A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169196 | ||||||
chr1:185169227
|
C | G | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.224+829C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169227 | ||||||
chr1:185169276
|
A | G | 1 | a0002c0002t0001g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.224+878A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169276 | ||||||
chr1:185169279
|
CT | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0088others(15): Show | 18 | HG00621.hp2 HG01123.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.224+898delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185169279 | |||||
chr1:185169540
|
A | G | 1 | a0003c0003t0001g0213 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.224+1142A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185169540 | ||||||
chr1:185169780
|
AT | A | 19 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(16): Show | 19 | HG00438.hp1 HG02071.hp2 HG03486.hp2 others(16): Show |
intron_variant | MODIFIER | c.224+1397delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185169780 | |||||
chr1:185170074
|
C | T | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(15): Show |
intron_variant | MODIFIER | c.224+1676C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170074 | ||||||
chr1:185170183
|
G | A | 1 | a0002c0004t0001g0297 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.224+1785G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170183 | ||||||
chr1:185170221
|
G | A | 47 | a0002c0004t0001g0010a0002c0004t0001g0289a0002c0004t0001g0292others(44): Show | 48 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.224+1823G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170221 | ||||||
chr1:185170249
|
T | C | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(15): Show |
intron_variant | MODIFIER | c.224+1851T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170249 | ||||||
chr1:185170400
|
C | T | 1 | a0007c0010t0010g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.224+2002C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170400 | ||||||
chr1:185170402
|
A | G | 1 | a0003c0005t0003g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.224+2004A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170402 | ||||||
chr1:185170519
|
A | G | 1 | a0002c0002t0001g0219 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.224+2121A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170519 | ||||||
chr1:185170732
|
G | A | 321 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(318): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.224+2334G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170732 | ||||||
chr1:185170797
|
C | T | 5 | a0003c0005t0001g0014a0003c0005t0003g0228a0008c0012t0001g0019others(2): Show | 5 | HG02145.hp2 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+2399C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170797 | ||||||
chr1:185170830
|
T | G | 1 | a0005c0007t0001g0323 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.224+2432T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170830 | ||||||
chr1:185170971
|
T | C | 1 | a0002c0004t0001g0297 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.224+2573T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185170971 | ||||||
chr1:185171160
|
GA | G | 121 | a0001c0001t0001g0083a0001c0001t0001g0123a0001c0001t0002g0283others(118): Show | 122 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.224+2774delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185171160 | |||||
chr1:185171162
|
A | G | 2 | a0003c0003t0001g0263a0003c0003t0001g0264 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.224+2764A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171162 | ||||||
chr1:185171203
|
G | A | 1 | a0002c0004t0001g0087 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.224+2805G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171203 | ||||||
chr1:185171265
|
G | C | 1 | a0006c0014t0001g0293 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.224+2867G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171265 | ||||||
chr1:185171322
|
C | A | 1 | a0001c0001t0002g0283 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.224+2924C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171322 | ||||||
chr1:185171323
|
A | T | 1 | a0001c0001t0002g0283 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.224+2925A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171323 | ||||||
chr1:185171530
|
A | G | 61 | a0001c0001t0001g0026a0001c0001t0002g0122a0002c0004t0001g0010others(58): Show | 62 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(59): Show |
intron_variant | MODIFIER | c.225-2842A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171530 | ||||||
chr1:185171609
|
A | G | 12 | a0003c0005t0004g0007a0003c0005t0004g0008a0003c0005t0004g0230others(9): Show | 12 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.225-2763A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171609 | ||||||
chr1:185171663
|
T | G | 3 | a0003c0005t0001g0231a0003c0005t0001g0232a0003c0005t0009g0004 | 3 | HG01243.hp1 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.225-2709T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171663 | ||||||
chr1:185171735
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.225-2637A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171735 | ||||||
chr1:185171799
|
A | G | 3 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247 | 4 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-2573A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171799 | ||||||
chr1:185171981
|
T | C | 1 | a0001c0001t0002g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.225-2391T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185171981 | ||||||
chr1:185172183
|
TC | T | 7 | a0002c0004t0001g0316a0002c0004t0001g0317a0002c0004t0001g0318others(4): Show | 7 | NA18948.hp1 NA18967.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-2185delC | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185172183 | |||||
chr1:185172192
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.225-2180T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172192 | ||||||
chr1:185172276
|
G | T | 26 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(23): Show | 26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.225-2096G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172276 | ||||||
chr1:185172382
|
T | C | 1 | a0004c0006t0001g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.225-1990T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172382 | ||||||
chr1:185172603
|
G | C | 2 | a0001c0001t0001g0129a0012c0018t0001g0029 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.225-1769G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172603 | ||||||
chr1:185172695
|
A | G | 161 | a0001c0001t0001g0082a0002c0002t0001g0002a0002c0002t0001g0136others(158): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.225-1677A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172695 | ||||||
chr1:185172711
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.225-1661C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172711 | ||||||
chr1:185172831
|
G | A | 2 | a0002c0004t0001g0300a0002c0004t0001g0301 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.225-1541G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185172831 | ||||||
chr1:185173020
|
G | A | 160 | a0001c0001t0001g0082a0002c0002t0001g0002a0002c0002t0001g0136others(157): Show | 162 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.225-1352G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173020 | ||||||
chr1:185173042
|
C | CA | 160 | a0001c0001t0001g0031a0001c0001t0001g0097a0001c0001t0001g0123others(157): Show | 162 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.225-1311dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185173042 | |||||
chr1:185173042
|
C | CAA | 6 | a0001c0001t0001g0096a0001c0001t0002g0011a0001c0001t0002g0122others(3): Show | 6 | HG01361.hp1 HG02074.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-1312_225-1311d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185173042 | |||||
chr1:185173200
|
G | A | 179 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(176): Show | 181 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.225-1172G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173200 | ||||||
chr1:185173376
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.225-996G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173376 | ||||||
chr1:185173379
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.225-993T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173379 | ||||||
chr1:185173412
|
G | A | 3 | a0002c0002t0001g0136a0002c0002t0001g0137a0002c0002t0001g0256 | 3 | HG02451.hp2 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.225-960G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173412 | ||||||
chr1:185173456
|
A | T | 40 | a0002c0002t0001g0215a0002c0002t0001g0216a0002c0004t0001g0010others(37): Show | 40 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.225-916A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173456 | ||||||
chr1:185173492
|
C | T | 1 | a0008c0012t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.225-880C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173492 | ||||||
chr1:185173530
|
C | CA | 11 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG00597.hp2 HG01081.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-821dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185173530 | |||||
chr1:185173530
|
CA | C | 46 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0030others(43): Show | 47 | HG00438.hp1 HG01243.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.225-821delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185173530 | |||||
chr1:185173530
|
CAA | C | 128 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(125): Show | 129 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.225-822_225-821del others(2): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 185173530 | |||||
chr1:185173582
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.225-790A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173582 | ||||||
chr1:185173638
|
T | C | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.225-734T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173638 | ||||||
chr1:185173681
|
C | T | 2 | a0002c0004t0001g0314a0002c0004t0001g0315 | 2 | HG02040.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.225-691C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173681 | ||||||
chr1:185173738
|
G | A | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.225-634G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 4/18 | chr1 | 185173738 | ||||||
chr1:185175202
|
G | GT | 19 | a0001c0001t0002g0011a0001c0001t0002g0013a0001c0001t0002g0030others(16): Show | 19 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.966+104dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185175202 | |||||
chr1:185175202
|
GT | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0040a0003c0003t0001g0155others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.966+104delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185175202 | |||||
chr1:185175215
|
T | G | 168 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0036others(165): Show | 170 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.966+102T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175215 | ||||||
chr1:185175215
|
T | TG | 4 | a0001c0001t0002g0284a0002c0002t0001g0217a0002c0002t0001g0218others(1): Show | 4 | NA18961.hp2 NA19001.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+102_966+103ins others(1): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175215 | ||||||
chr1:185175228
|
G | T | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.966+115G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175228 | ||||||
chr1:185175381
|
C | T | 1 | a0002c0002t0001g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.966+268C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175381 | ||||||
chr1:185175414
|
A | T | 2 | a0001c0001t0001g0080a0004c0009t0001g0081 | 2 | NA18954.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.966+301A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175414 | ||||||
chr1:185175496
|
G | A | 1 | a0006c0008t0003g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.966+383G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175496 | ||||||
chr1:185175507
|
C | T | 1 | a0008c0012t0001g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.966+394C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175507 | ||||||
chr1:185175522
|
A | G | 14 | a0003c0005t0001g0014a0003c0005t0003g0228a0003c0005t0004g0007others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.966+409A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175522 | ||||||
chr1:185175616
|
C | A | 4 | a0001c0001t0001g0006a0008c0012t0001g0019a0008c0012t0001g0020others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+503C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175616 | ||||||
chr1:185175752
|
C | CAG | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.966+639_966+640ins others(2): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175752 | ||||||
chr1:185175826
|
A | G | 1 | a0003c0003t0001g0211 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.966+713A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185175826 | ||||||
chr1:185176286
|
CA | C | 174 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0031others(171): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.966+1201delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176286 | |||||
chr1:185176286
|
CAA | C | 42 | a0001c0001t0001g0120a0001c0001t0001g0129a0001c0001t0002g0012others(39): Show | 42 | HG00438.hp1 HG01167.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.966+1200_966+1201d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176286 | |||||
chr1:185176286
|
CAAAAAAA others(6): Show |
C | 1 | a0004c0006t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.966+1189_966+1201d others(15): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176286 | |||||
chr1:185176286
|
CAAAAAAA others(8): Show |
C | 24 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(21): Show | 24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.966+1187_966+1201d others(17): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176286 | |||||
chr1:185176347
|
AAC | A | 9 | a0003c0005t0004g0007a0003c0005t0004g0008a0003c0005t0004g0230others(6): Show | 9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+1236_966+1237d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176347 | |||||
chr1:185176385
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.966+1272G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185176385 | ||||||
chr1:185176798
|
C | T | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.966+1685C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185176798 | ||||||
chr1:185176978
|
C | T | 1 | a0003c0003t0001g0190 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.966+1865C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185176978 | ||||||
chr1:185176983
|
T | TA | 107 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(104): Show | 108 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.966+1888dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 185176983 | |||||
chr1:185177266
|
T | A | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.966+2153T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185177266 | ||||||
chr1:185177412
|
T | A | 1 | a0003c0005t0004g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.966+2299T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185177412 | ||||||
chr1:185177649
|
T | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.966+2536T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185177649 | ||||||
chr1:185177653
|
C | A | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+2540C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185177653 | ||||||
chr1:185177804
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.967-2587A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185177804 | ||||||
chr1:185178142
|
A | G | 179 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(176): Show | 181 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.967-2249A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178142 | ||||||
chr1:185178162
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.967-2229T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178162 | ||||||
chr1:185178207
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.967-2184T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178207 | ||||||
chr1:185178410
|
C | T | 1 | a0001c0001t0002g0291 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.967-1981C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178410 | ||||||
chr1:185178466
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.967-1925G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178466 | ||||||
chr1:185178602
|
T | C | 9 | a0003c0005t0004g0007a0003c0005t0004g0008a0003c0005t0004g0230others(6): Show | 9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.967-1789T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178602 | ||||||
chr1:185178715
|
T | A | 321 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(318): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.967-1676T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178715 | ||||||
chr1:185178737
|
GCACTTCT others(43): Show |
G | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.967-1653_967-1604d others(52): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178737 | ||||||
chr1:185178828
|
A | T | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.967-1563A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185178828 | ||||||
chr1:185179140
|
G | A | 2 | a0003c0003t0001g0155a0003c0003t0001g0156 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.967-1251G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179140 | ||||||
chr1:185179255
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.967-1136C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179255 | ||||||
chr1:185179367
|
A | G | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.967-1024A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179367 | ||||||
chr1:185179377
|
C | T | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.967-1014C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179377 | ||||||
chr1:185179557
|
A | G | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.967-834A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179557 | ||||||
chr1:185179752
|
C | A | 322 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(319): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.967-639C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179752 | ||||||
chr1:185179760
|
T | G | 2 | a0003c0003t0001g0263a0003c0003t0001g0264 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.967-631T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185179760 | ||||||
chr1:185180004
|
G | C | 1 | a0004c0006t0001g0148 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.967-387G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185180004 | ||||||
chr1:185180131
|
T | C | 183 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(180): Show | 185 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.967-260T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185180131 | ||||||
chr1:185180221
|
A | G | 2 | a0006c0008t0003g0244a0006c0008t0003g0245 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.967-170A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 5/18 | chr1 | 185180221 | ||||||
chr1:185180813
|
A | T | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1026+363A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 6/18 | chr1 | 185180813 | ||||||
chr1:185181478
|
A | G | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1027-468A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 6/18 | chr1 | 185181478 | ||||||
chr1:185182246
|
T | G | 28 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0096others(25): Show | 28 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.1138+189T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182246 | ||||||
chr1:185182266
|
G | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1138+209G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182266 | ||||||
chr1:185182379
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1138+322T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182379 | ||||||
chr1:185182538
|
G | A | 91 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(88): Show | 92 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.1138+481G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182538 | ||||||
chr1:185182664
|
C | G | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138+607C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182664 | ||||||
chr1:185182668
|
CA | C | 136 | a0001c0001t0001g0060a0001c0001t0002g0011a0001c0001t0002g0012others(133): Show | 137 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1138+635delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr1 | 185182668 | |||||
chr1:185182668
|
CAA | C | 39 | a0002c0002t0001g0216a0002c0002t0001g0288a0002c0004t0001g0301others(36): Show | 39 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1138+634_1138+635d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr1 | 185182668 | |||||
chr1:185182689
|
AAAAG | A | 7 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0039others(4): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.1138+639_1138+642d others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr1 | 185182689 | |||||
chr1:185182862
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1138+805A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182862 | ||||||
chr1:185182873
|
C | T | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138+816C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182873 | ||||||
chr1:185182983
|
A | G | 2 | a0002c0004t0001g0027a0002c0004t0001g0028 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1138+926A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185182983 | ||||||
chr1:185183028
|
T | G | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1138+971T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183028 | ||||||
chr1:185183059
|
C | A | 2 | a0003c0003t0001g0271a0003c0003t0001g0272 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1138+1002C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183059 | ||||||
chr1:185183137
|
CA | C | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1139-1091delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr1 | 185183137 | |||||
chr1:185183287
|
G | T | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(6): Show | 9 | NA18949.hp2 NA18964.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.1139-956G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183287 | ||||||
chr1:185183318
|
G | A | 137 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(134): Show | 138 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1139-925G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183318 | ||||||
chr1:185183470
|
C | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1139-773C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183470 | ||||||
chr1:185183527
|
C | T | 1 | a0004c0006t0001g0148 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1139-716C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183527 | ||||||
chr1:185183634
|
G | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1139-609G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183634 | ||||||
chr1:185183868
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1139-375A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183868 | ||||||
chr1:185183945
|
T | G | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1139-298T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183945 | ||||||
chr1:185183975
|
C | T | 6 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(3): Show | 6 | NA18964.hp2 NA18972.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.1139-268C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185183975 | ||||||
chr1:185184068
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1139-175C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185184068 | ||||||
chr1:185184070
|
G | T | 1 | a0003c0003t0001g0264 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1139-173G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 7/18 | chr1 | 185184070 | ||||||
chr1:185184413
|
G | GT | 179 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(176): Show | 181 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1240+69_1240+70ins others(1): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 8/18 | chr1 | 185184413 | ||||||
chr1:185184433
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1240+89A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 8/18 | chr1 | 185184433 | ||||||
chr1:185184514
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1240+170T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 8/18 | chr1 | 185184514 | ||||||
chr1:185184942
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1429+11T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185184942 | ||||||
chr1:185184993
|
T | C | 2 | a0003c0021t0011g0132a0015c0022t0001g0009 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1429+62T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185184993 | ||||||
chr1:185185015
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1429+84T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185185015 | ||||||
chr1:185185191
|
G | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1429+260G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185185191 | ||||||
chr1:185185217
|
A | G | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1429+286A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185185217 | ||||||
chr1:185185365
|
T | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG01099.hp1 HG01256.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+434T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185185365 | ||||||
chr1:185185996
|
G | C | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1429+1065G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185185996 | ||||||
chr1:185186139
|
T | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG00140.hp1 HG01081.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+1208T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186139 | ||||||
chr1:185186383
|
A | G | 1 | a0004c0006t0001g0145 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1429+1452A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186383 | ||||||
chr1:185186418
|
G | A | 2 | a0002c0004t0001g0010a0002c0004t0001g0292 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1429+1487G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186418 | ||||||
chr1:185186683
|
G | A | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1429+1752G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186683 | ||||||
chr1:185186795
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0277 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1429+1864C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186795 | ||||||
chr1:185186916
|
G | A | 2 | a0003c0003t0001g0263a0003c0003t0001g0264 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1429+1985G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185186916 | ||||||
chr1:185187029
|
A | G | 33 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(30): Show | 33 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1429+2098A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187029 | ||||||
chr1:185187053
|
C | CT | 284 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(281): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1429+2141dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185187053 | |||||
chr1:185187053
|
C | CTT | 11 | a0001c0001t0001g0037a0001c0011t0001g0149a0001c0011t0008g0261others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1429+2140_1429+214 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185187053 | |||||
chr1:185187062
|
T | TTTTTTTT others(288): Show |
15 | a0001c0001t0002g0013a0001c0001t0002g0030a0001c0001t0002g0274others(12): Show | 15 | HG00438.hp1 HG02071.hp2 HG03654.hp1 others(12): Show |
intron_variant | MODIFIER | c.1429+2141_1429+214 others(299): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185187062 | |||||
chr1:185187062
|
T | TTTTTTTT others(289): Show |
4 | a0001c0001t0002g0011a0001c0001t0002g0122a0001c0001t0002g0276others(1): Show | 4 | HG02074.hp1 NA18949.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+2141_1429+214 others(300): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185187062 | |||||
chr1:185187062
|
T | TTTTTTTT others(290): Show |
1 | a0001c0001t0002g0012 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1429+2141_1429+214 others(301): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185187062 | |||||
chr1:185187073
|
A | T | 28 | a0001c0001t0001g0022a0003c0003t0001g0155a0003c0003t0001g0156others(25): Show | 28 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.1429+2142A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187073 | ||||||
chr1:185187241
|
G | A | 1 | a0006c0014t0001g0295 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1429+2310G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187241 | ||||||
chr1:185187248
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1429+2317T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187248 | ||||||
chr1:185187342
|
G | A | 1 | a0015c0022t0001g0009 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1429+2411G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187342 | ||||||
chr1:185187711
|
T | G | 1 | a0003c0003t0001g0192 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1429+2780T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187711 | ||||||
chr1:185187771
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1430-2778G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187771 | ||||||
chr1:185187832
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0042 | 4 | HG00738.hp1 HG01261.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1430-2717G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187832 | ||||||
chr1:185187984
|
C | T | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1430-2565C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187984 | ||||||
chr1:185187999
|
C | A | 183 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(180): Show | 185 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1430-2550C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185187999 | ||||||
chr1:185188050
|
A | G | 1 | a0002c0002t0001g0151 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1430-2499A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188050 | ||||||
chr1:185188172
|
TCTTTATT others(7): Show |
T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1430-2361_1430-234 others(18): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 185188172 | |||||
chr1:185188227
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1430-2322T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188227 | ||||||
chr1:185188337
|
G | A | 2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1430-2212G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188337 | ||||||
chr1:185188568
|
T | C | 179 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(176): Show | 181 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1430-1981T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188568 | ||||||
chr1:185188633
|
G | A | 2 | a0003c0003t0001g0155a0003c0003t0001g0156 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1430-1916G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188633 | ||||||
chr1:185188710
|
G | A | 5 | a0003c0005t0001g0014a0003c0005t0003g0228a0003c0005t0009g0004others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1430-1839G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188710 | ||||||
chr1:185188917
|
A | G | 1 | a0006c0014t0001g0295 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1430-1632A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185188917 | ||||||
chr1:185189232
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1430-1317C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185189232 | ||||||
chr1:185189422
|
C | A | 24 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(21): Show | 24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1430-1127C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185189422 | ||||||
chr1:185190341
|
A | G | 1 | a0002c0002t0001g0186 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1430-208A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 9/18 | chr1 | 185190341 | ||||||
chr1:185190862
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1523+220G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185190862 | ||||||
chr1:185190910
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1523+268C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185190910 | ||||||
chr1:185191023
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+381A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191023 | ||||||
chr1:185191067
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+425T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191067 | ||||||
chr1:185191255
|
G | A | 5 | a0003c0005t0001g0014a0003c0005t0003g0228a0003c0005t0009g0004others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1523+613G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191255 | ||||||
chr1:185191304
|
C | G | 1 | a0004c0006t0001g0163 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1523+662C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191304 | ||||||
chr1:185191337
|
T | A | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+695T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191337 | ||||||
chr1:185191467
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+825T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191467 | ||||||
chr1:185191669
|
T | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1523+1027T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191669 | ||||||
chr1:185191744
|
A | G | 1 | a0002c0004t0001g0311 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1523+1102A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191744 | ||||||
chr1:185191805
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1523+1163A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191805 | ||||||
chr1:185191857
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+1215A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191857 | ||||||
chr1:185191905
|
C | A | 1 | a0004c0006t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1523+1263C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185191905 | ||||||
chr1:185192278
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG01099.hp1 HG01256.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+1636C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192278 | ||||||
chr1:185192380
|
G | T | 1 | a0003c0003t0001g0209 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1523+1738G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192380 | ||||||
chr1:185192396
|
C | T | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1523+1754C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192396 | ||||||
chr1:185192451
|
T | C | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+1809T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192451 | ||||||
chr1:185192535
|
C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1523+1893C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192535 | ||||||
chr1:185192586
|
C | G | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1523+1944C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192586 | ||||||
chr1:185192738
|
C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1523+2096C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192738 | ||||||
chr1:185192891
|
G | A | 4 | a0003c0005t0003g0248a0003c0005t0003g0249a0003c0005t0003g0250others(1): Show | 4 | HG02055.hp2 HG02723.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+2249G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192891 | ||||||
chr1:185192925
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2283A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185192925 | ||||||
chr1:185193097
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2455G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193097 | ||||||
chr1:185193462
|
C | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0277 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1523+2820C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193462 | ||||||
chr1:185193467
|
C | CT | 17 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(14): Show | 18 | HG02055.hp2 HG02451.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.1523+2839dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185193467 | |||||
chr1:185193467
|
C | CTT | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2838_1523+283 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185193467 | |||||
chr1:185193472
|
T | C | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+2830T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193472 | ||||||
chr1:185193501
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2859T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193501 | ||||||
chr1:185193562
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2920A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193562 | ||||||
chr1:185193630
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+2988A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193630 | ||||||
chr1:185193657
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1523+3015G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193657 | ||||||
chr1:185193687
|
G | T | 131 | a0001c0001t0002g0122a0001c0001t0002g0279a0001c0011t0001g0149others(128): Show | 132 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1523+3045G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193687 | ||||||
chr1:185193751
|
C | T | 1 | a0002c0002t0001g0185 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1523+3109C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193751 | ||||||
chr1:185193963
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1523+3321T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193963 | ||||||
chr1:185193969
|
G | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+3327G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185193969 | ||||||
chr1:185194190
|
A | G | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523+3548A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194190 | ||||||
chr1:185194324
|
T | A | 1 | a0003c0021t0011g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1523+3682T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194324 | ||||||
chr1:185194366
|
G | T | 178 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(175): Show | 180 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1523+3724G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194366 | ||||||
chr1:185194527
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1523+3885G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194527 | ||||||
chr1:185194532
|
T | TTGCTGTT others(12): Show |
1 | a0005c0007t0001g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1523+3891_1523+390 others(23): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185194532 | |||||
chr1:185194571
|
T | TAA | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1523+3940_1523+394 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185194571 | |||||
chr1:185194576
|
A | T | 1 | a0005c0007t0001g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1523+3934A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194576 | ||||||
chr1:185194577
|
AAAAAAAG others(8): Show |
A | 1 | a0005c0007t0001g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1523+3936_1523+395 others(19): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194577 | ||||||
chr1:185194603
|
T | G | 1 | a0005c0007t0001g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1523+3961T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194603 | ||||||
chr1:185194664
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+4022A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194664 | ||||||
chr1:185194752
|
T | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0277 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1523+4110T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194752 | ||||||
chr1:185194975
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1523+4333C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185194975 | ||||||
chr1:185195128
|
C | G | 1 | a0008c0012t0001g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1523+4486C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195128 | ||||||
chr1:185195172
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1523+4530C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195172 | ||||||
chr1:185195246
|
G | A | 160 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(157): Show | 162 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1523+4604G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195246 | ||||||
chr1:185195447
|
C | T | 2 | a0009c0017t0001g0076a0009c0023t0001g0162 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1523+4805C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195447 | ||||||
chr1:185195661
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1523+5019T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195661 | ||||||
chr1:185195713
|
C | A | 2 | a0003c0003t0001g0263a0003c0003t0001g0264 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1523+5071C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195713 | ||||||
chr1:185195714
|
A | G | 2 | a0003c0003t0001g0263a0003c0003t0001g0264 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1523+5072A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195714 | ||||||
chr1:185195771
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1523+5129T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195771 | ||||||
chr1:185195785
|
T | C | 1 | a0003c0003t0001g0237 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1523+5143T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195785 | ||||||
chr1:185195843
|
T | G | 1 | a0003c0005t0001g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1523+5201T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195843 | ||||||
chr1:185195978
|
C | A | 1 | a0001c0001t0001g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1523+5336C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185195978 | ||||||
chr1:185196085
|
G | T | 1 | a0003c0003t0001g0209 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1523+5443G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196085 | ||||||
chr1:185196133
|
G | A | 2 | a0001c0001t0001g0080a0004c0009t0001g0081 | 2 | NA18954.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1523+5491G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196133 | ||||||
chr1:185196291
|
T | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1523+5649T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196291 | ||||||
chr1:185196323
|
C | G | 1 | a0002c0002t0001g0186 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1523+5681C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196323 | ||||||
chr1:185196408
|
G | T | 1 | a0004c0009t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1523+5766G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196408 | ||||||
chr1:185196725
|
A | G | 2 | a0003c0003t0001g0155a0003c0003t0001g0156 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1524-5929A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196725 | ||||||
chr1:185196842
|
T | C | 1 | a0001c0001t0002g0290 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1524-5812T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196842 | ||||||
chr1:185196996
|
A | G | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-5658A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185196996 | ||||||
chr1:185197194
|
G | A | 1 | a0002c0004t0001g0311 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1524-5460G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197194 | ||||||
chr1:185197430
|
T | TC | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-5224_1524-522 others(5): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197430 | ||||||
chr1:185197484
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1524-5170G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197484 | ||||||
chr1:185197534
|
G | T | 4 | a0001c0001t0001g0006a0008c0012t0001g0019a0008c0012t0001g0020others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524-5120G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197534 | ||||||
chr1:185197558
|
T | C | 1 | a0001c0001t0006g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1524-5096T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197558 | ||||||
chr1:185197653
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-5001A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197653 | ||||||
chr1:185197685
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-4969T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197685 | ||||||
chr1:185197791
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-4863T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197791 | ||||||
chr1:185197819
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1524-4835T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197819 | ||||||
chr1:185197879
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00597.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1524-4775A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185197879 | ||||||
chr1:185198010
|
C | T | 4 | a0007c0010t0001g0071a0007c0010t0001g0072a0007c0010t0001g0073others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-4644C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198010 | ||||||
chr1:185198075
|
A | G | 1 | a0003c0005t0003g0246 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1524-4579A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198075 | ||||||
chr1:185198111
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-4543G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198111 | ||||||
chr1:185198213
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1524-4441A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198213 | ||||||
chr1:185198224
|
C | T | 1 | a0004c0006t0001g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1524-4430C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198224 | ||||||
chr1:185198236
|
C | T | 1 | a0003c0005t0004g0267 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1524-4418C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198236 | ||||||
chr1:185198326
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1524-4328T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198326 | ||||||
chr1:185198352
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1524-4302C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198352 | ||||||
chr1:185198626
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-4028C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198626 | ||||||
chr1:185198680
|
G | C | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-3974G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198680 | ||||||
chr1:185198707
|
C | T | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-3947C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198707 | ||||||
chr1:185198752
|
G | A | 1 | a0004c0006t0001g0153 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1524-3902G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198752 | ||||||
chr1:185198762
|
G | GT | 15 | a0001c0001t0001g0026a0001c0001t0001g0059a0002c0002t0001g0152others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1524-3880dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185198762 | |||||
chr1:185198775
|
G | T | 12 | a0001c0001t0001g0134a0003c0005t0003g0003a0003c0005t0003g0246others(9): Show | 13 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1524-3879G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198775 | ||||||
chr1:185198863
|
G | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-3791G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185198863 | ||||||
chr1:185198938
|
AT | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0002g0030others(5): Show | 8 | HG00438.hp2 HG01884.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.1524-3698delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185198938 | |||||
chr1:185198938
|
ATT | A | 17 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(14): Show | 17 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1524-3699_1524-369 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185198938 | |||||
chr1:185199094
|
T | G | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-3560T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199094 | ||||||
chr1:185199128
|
G | A | 5 | a0003c0005t0001g0014a0003c0005t0003g0228a0003c0005t0009g0004others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524-3526G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199128 | ||||||
chr1:185199171
|
C | T | 5 | a0004c0006t0001g0159a0004c0006t0001g0166a0004c0006t0001g0223others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524-3483C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199171 | ||||||
chr1:185199383
|
G | A | 1 | a0002c0002t0001g0218 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1524-3271G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199383 | ||||||
chr1:185199435
|
G | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1524-3219G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199435 | ||||||
chr1:185199469
|
G | A | 2 | a0003c0003t0001g0193a0003c0003t0001g0194 | 2 | HG00408.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1524-3185G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199469 | ||||||
chr1:185199523
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-3131T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199523 | ||||||
chr1:185199625
|
C | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-3029C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199625 | ||||||
chr1:185199662
|
C | T | 4 | a0001c0001t0001g0006a0008c0012t0001g0019a0008c0012t0001g0020others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524-2992C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199662 | ||||||
chr1:185199831
|
A | C | 2 | a0002c0004t0001g0010a0002c0004t0001g0292 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1524-2823A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199831 | ||||||
chr1:185199901
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-2753C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185199901 | ||||||
chr1:185200041
|
G | A | 81 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(78): Show | 82 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1524-2613G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200041 | ||||||
chr1:185200317
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG00621.hp2 HG01952.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524-2337G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200317 | ||||||
chr1:185200531
|
G | T | 1 | a0003c0005t0003g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1524-2123G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200531 | ||||||
chr1:185200595
|
G | A | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-2059G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200595 | ||||||
chr1:185200673
|
G | T | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-1981G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200673 | ||||||
chr1:185200768
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1524-1886C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200768 | ||||||
chr1:185200805
|
G | C | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-1849G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200805 | ||||||
chr1:185200809
|
C | T | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-1845C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200809 | ||||||
chr1:185200864
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-1790C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185200864 | ||||||
chr1:185201002
|
C | T | 2 | a0001c0001t0005g0100a0003c0005t0004g0008 | 2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1524-1652C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201002 | ||||||
chr1:185201015
|
C | T | 1 | a0010c0013t0001g0075 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1524-1639C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201015 | ||||||
chr1:185201227
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-1427T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201227 | ||||||
chr1:185201230
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-1424G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201230 | ||||||
chr1:185201244
|
C | T | 2 | a0004c0009t0001g0113a0004c0009t0001g0114 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1524-1410C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201244 | ||||||
chr1:185201285
|
C | T | 1 | a0007c0010t0010g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1524-1369C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201285 | ||||||
chr1:185201342
|
C | T | 139 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(136): Show | 140 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1524-1312C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201342 | ||||||
chr1:185201406
|
C | T | 1 | a0001c0011t0008g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1524-1248C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201406 | ||||||
chr1:185201415
|
G | A | 1 | a0003c0005t0003g0252 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1524-1239G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201415 | ||||||
chr1:185201539
|
G | A | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524-1115G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201539 | ||||||
chr1:185201696
|
T | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-958T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201696 | ||||||
chr1:185201706
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0060 | 2 | NA18612.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1524-948C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201706 | ||||||
chr1:185201785
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1524-869C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185201785 | ||||||
chr1:185201946
|
AT | A | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-698delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185201946 | |||||
chr1:185202135
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-519A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185202135 | ||||||
chr1:185202455
|
T | TTA | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524-184_1524-183d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 185202455 | |||||
chr1:185202547
|
G | A | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1524-107G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 10/18 | chr1 | 185202547 | ||||||
chr1:185202816
|
A | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1669+17A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185202816 | ||||||
chr1:185203240
|
C | CCTT | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1669+443_1669+444i others(5): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 185203240 | |||||
chr1:185203352
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1669+553A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203352 | ||||||
chr1:185203362
|
G | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1669+563G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203362 | ||||||
chr1:185203428
|
G | A | 22 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(19): Show | 22 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1669+629G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203428 | ||||||
chr1:185203443
|
C | A | 185 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(182): Show | 187 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.1669+644C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203443 | ||||||
chr1:185203482
|
G | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1669+683G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203482 | ||||||
chr1:185203616
|
C | T | 51 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(48): Show | 52 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.1669+817C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203616 | ||||||
chr1:185203648
|
A | G | 5 | a0003c0005t0001g0014a0003c0005t0003g0228a0003c0005t0009g0004others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1669+849A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203648 | ||||||
chr1:185203905
|
A | G | 139 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(136): Show | 140 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1670-795A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185203905 | ||||||
chr1:185204058
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1670-642C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185204058 | ||||||
chr1:185204171
|
G | A | 2 | a0002c0004t0001g0010a0002c0004t0001g0292 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1670-529G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185204171 | ||||||
chr1:185204263
|
C | T | 4 | a0001c0001t0001g0006a0008c0012t0001g0019a0008c0012t0001g0020others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670-437C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185204263 | ||||||
chr1:185204575
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1670-125T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185204575 | ||||||
chr1:185204585
|
A | G | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1670-115A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 11/18 | chr1 | 185204585 | ||||||
chr1:185204986
|
T | C | 1 | a0002c0002t0001g0171 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1833+123T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185204986 | ||||||
chr1:185205075
|
A | T | 63 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0033others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1833+212A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205075 | ||||||
chr1:185205078
|
CAG | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1833+217_1833+218d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 185205078 | |||||
chr1:185205390
|
C | T | 1 | a0003c0005t0004g0270 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1833+527C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205390 | ||||||
chr1:185205406
|
T | C | 6 | a0003c0005t0003g0248a0003c0005t0003g0249a0003c0005t0003g0250others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1833+543T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205406 | ||||||
chr1:185205709
|
A | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1833+846A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205709 | ||||||
chr1:185205717
|
T | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1833+854T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205717 | ||||||
chr1:185205729
|
A | T | 1 | a0001c0001t0002g0274 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1833+866A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205729 | ||||||
chr1:185205884
|
C | T | 35 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1834-741C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205884 | ||||||
chr1:185205980
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1834-645T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185205980 | ||||||
chr1:185206131
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1834-494G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185206131 | ||||||
chr1:185206228
|
A | G | 1 | a0004c0006t0001g0223 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1834-397A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185206228 | ||||||
chr1:185206412
|
C | T | 1 | a0003c0005t0003g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834-213C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 12/18 | chr1 | 185206412 | ||||||
chr1:185206772
|
C | G | 2 | a0003c0021t0011g0132a0015c0022t0001g0009 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1972+9C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185206772 | ||||||
chr1:185206883
|
A | G | 161 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(158): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1972+120A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185206883 | ||||||
chr1:185207191
|
G | C | 2 | a0002c0002t0001g0215a0002c0002t0001g0216 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1972+428G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207191 | ||||||
chr1:185207263
|
G | A | 104 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(101): Show | 105 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(102): Show |
intron_variant | MODIFIER | c.1972+500G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207263 | ||||||
chr1:185207373
|
G | C | 1 | a0003c0003t0001g0212 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1972+610G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207373 | ||||||
chr1:185207469
|
A | G | 2 | a0010c0013t0001g0074a0010c0013t0001g0075 | 2 | NA18977.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1972+706A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207469 | ||||||
chr1:185207470
|
A | C | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1972+707A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207470 | ||||||
chr1:185207620
|
G | A | 1 | a0007c0010t0010g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1972+857G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207620 | ||||||
chr1:185207761
|
G | A | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1972+998G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207761 | ||||||
chr1:185207849
|
C | T | 36 | a0002c0002t0001g0002a0002c0002t0001g0151a0002c0002t0001g0152others(33): Show | 37 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1972+1086C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185207849 | ||||||
chr1:185208187
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1972+1424A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208187 | ||||||
chr1:185208248
|
A | G | 1 | a0003c0003t0001g0207 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1972+1485A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208248 | ||||||
chr1:185208379
|
A | G | 1 | a0002c0002t0001g0217 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1972+1616A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208379 | ||||||
chr1:185208392
|
A | G | 1 | a0003c0021t0011g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1972+1629A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208392 | ||||||
chr1:185208649
|
AAAGT | A | 11 | a0002c0004t0001g0289a0002c0004t0001g0294a0002c0004t0001g0303others(8): Show | 11 | HG01255.hp1 HG01496.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1972+1891_1972+189 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185208649 | |||||
chr1:185208652
|
G | C | 1 | a0001c0011t0008g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1972+1889G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208652 | ||||||
chr1:185208659
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1972+1896G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208659 | ||||||
chr1:185208675
|
C | T | 4 | a0001c0001t0001g0006a0008c0012t0001g0019a0008c0012t0001g0020others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1972+1912C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208675 | ||||||
chr1:185208726
|
G | A | 2 | a0009c0017t0001g0076a0009c0023t0001g0162 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1972+1963G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208726 | ||||||
chr1:185208742
|
C | CT | 74 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(71): Show | 75 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1972+1993dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185208742 | |||||
chr1:185208742
|
C | CTT | 35 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1972+1992_1972+199 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185208742 | |||||
chr1:185208759
|
T | A | 36 | a0002c0002t0001g0002a0002c0002t0001g0151a0002c0002t0001g0152others(33): Show | 37 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1972+1996T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208759 | ||||||
chr1:185208783
|
A | G | 24 | a0001c0011t0001g0149a0004c0006t0001g0143a0004c0006t0001g0144others(21): Show | 24 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1972+2020A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208783 | ||||||
chr1:185208811
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1972+2048G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208811 | ||||||
chr1:185208938
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1972+2175T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185208938 | ||||||
chr1:185208968
|
CACTGTT | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1972+2210_1972+221 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185208968 | |||||
chr1:185209019
|
G | A | 181 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(178): Show | 183 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1972+2256G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209019 | ||||||
chr1:185209303
|
C | T | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1972+2540C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209303 | ||||||
chr1:185209319
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1972+2556G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209319 | ||||||
chr1:185209323
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1972+2560C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209323 | ||||||
chr1:185209331
|
A | C | 1 | a0003c0003t0001g0208 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1972+2568A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209331 | ||||||
chr1:185209601
|
C | A | 1 | a0015c0022t0001g0009 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1972+2838C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209601 | ||||||
chr1:185209685
|
A | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0042 | 4 | HG00738.hp1 HG01261.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972+2922A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209685 | ||||||
chr1:185209727
|
T | C | 1 | a0002c0004t0001g0314 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1972+2964T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209727 | ||||||
chr1:185209730
|
G | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG02165.hp2 NA18612.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1972+2967G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209730 | ||||||
chr1:185209800
|
A | C | 161 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(158): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1972+3037A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209800 | ||||||
chr1:185209934
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1972+3171G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185209934 | ||||||
chr1:185210334
|
C | T | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1972+3571C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210334 | ||||||
chr1:185210420
|
G | A | 2 | a0009c0017t0001g0076a0009c0023t0001g0162 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1972+3657G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210420 | ||||||
chr1:185210545
|
A | G | 1 | a0003c0003t0004g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1972+3782A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210545 | ||||||
chr1:185210617
|
T | G | 1 | a0001c0001t0001g0025 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1972+3854T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210617 | ||||||
chr1:185210631
|
C | A | 1 | a0003c0005t0003g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1972+3868C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210631 | ||||||
chr1:185210781
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1973-3726G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185210781 | ||||||
chr1:185211020
|
C | CCGCT | 93 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(90): Show | 94 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(91): Show |
intron_variant | MODIFIER | c.1973-3486_1973-348 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185211020 | |||||
chr1:185211339
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1973-3168A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185211339 | ||||||
chr1:185211412
|
C | T | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1973-3095C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185211412 | ||||||
chr1:185211431
|
A | G | 1 | a0002c0002t0001g0183 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1973-3076A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185211431 | ||||||
chr1:185211769
|
T | C | 1 | a0002c0002t0001g0187 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1973-2738T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185211769 | ||||||
chr1:185211990
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1973-2517G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185211990 | ||||||
chr1:185212015
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1973-2492G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212015 | ||||||
chr1:185212352
|
C | G | 161 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(158): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1973-2155C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212352 | ||||||
chr1:185212376
|
A | C | 5 | a0003c0005t0004g0265a0003c0005t0004g0266a0003c0005t0004g0268others(2): Show | 5 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1973-2131A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212376 | ||||||
chr1:185212382
|
G | T | 5 | a0003c0005t0004g0265a0003c0005t0004g0266a0003c0005t0004g0268others(2): Show | 5 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1973-2125G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212382 | ||||||
chr1:185212395
|
C | T | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1973-2112C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212395 | ||||||
chr1:185212407
|
G | A | 2 | a0002c0002t0001g0173a0002c0002t0001g0174 | 2 | NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1973-2100G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212407 | ||||||
chr1:185212539
|
G | A | 1 | a0003c0005t0003g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1973-1968G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212539 | ||||||
chr1:185212589
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1973-1918C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212589 | ||||||
chr1:185212608
|
G | A | 1 | a0012c0018t0001g0029 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1973-1899G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212608 | ||||||
chr1:185212695
|
C | T | 1 | a0003c0003t0001g0209 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1973-1812C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212695 | ||||||
chr1:185212725
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1973-1782C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185212725 | ||||||
chr1:185212803
|
C | CA | 153 | a0001c0001t0001g0102a0002c0002t0001g0002a0002c0002t0001g0136others(150): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1973-1689dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185212803 | |||||
chr1:185212803
|
C | CAA | 9 | a0002c0004t0001g0303a0002c0004t0001g0318a0003c0003t0001g0190others(6): Show | 9 | HG01928.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1973-1690_1973-168 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185212803 | |||||
chr1:185212817
|
A | AAAT | 19 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0030others(16): Show | 19 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1973-1689_1973-168 others(7): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185212817 | |||||
chr1:185213086
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1973-1421C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185213086 | ||||||
chr1:185213138
|
CT | C | 10 | a0005c0007t0001g0242a0005c0007t0001g0243a0005c0007t0001g0296others(7): Show | 10 | NA18941.hp1 NA18970.hp1 NA18989.hp1 others(7): Show |
intron_variant | MODIFIER | c.1973-1365delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185213138 | |||||
chr1:185213205
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1973-1302G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185213205 | ||||||
chr1:185213555
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1973-952A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185213555 | ||||||
chr1:185213750
|
A | ATTAG | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1973-754_1973-753i others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 185213750 | |||||
chr1:185213917
|
A | G | 1 | a0001c0001t0002g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1973-590A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185213917 | ||||||
chr1:185214166
|
C | A | 2 | a0003c0003t0001g0192a0003c0003t0001g0195 | 2 | NA18977.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1973-341C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185214166 | ||||||
chr1:185214169
|
C | T | 2 | a0003c0003t0001g0192a0003c0003t0001g0195 | 2 | NA18977.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1973-338C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185214169 | ||||||
chr1:185214269
|
G | A | 1 | a0002c0002t0001g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1973-238G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 13/18 | chr1 | 185214269 | ||||||
chr1:185214698
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2121+43A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185214698 | ||||||
chr1:185214743
|
T | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0277 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2121+88T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185214743 | ||||||
chr1:185214776
|
G | A | 21 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(18): Show | 21 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2121+121G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185214776 | ||||||
chr1:185214840
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2121+185C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185214840 | ||||||
chr1:185215029
|
T | C | 14 | a0002c0004t0001g0297a0002c0004t0001g0302a0002c0004t0001g0308others(11): Show | 14 | HG03688.hp2 HG04228.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.2121+374T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215029 | ||||||
chr1:185215101
|
T | C | 162 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(159): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.2121+446T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215101 | ||||||
chr1:185215104
|
C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2121+449C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215104 | ||||||
chr1:185215383
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+728A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215383 | ||||||
chr1:185215559
|
A | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+904A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215559 | ||||||
chr1:185215587
|
C | T | 2 | a0002c0002t0001g0136a0002c0002t0001g0137 | 2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2121+932C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215587 | ||||||
chr1:185215678
|
A | G | 2 | a0002c0004t0001g0300a0002c0004t0001g0301 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2121+1023A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215678 | ||||||
chr1:185215691
|
C | T | 157 | a0001c0011t0001g0149a0002c0002t0001g0002a0002c0002t0001g0136others(154): Show | 159 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.2121+1036C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215691 | ||||||
chr1:185215765
|
C | T | 2 | a0004c0009t0001g0113a0004c0009t0001g0114 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2121+1110C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215765 | ||||||
chr1:185215806
|
T | C | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2121+1151T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215806 | ||||||
chr1:185215922
|
G | A | 5 | a0003c0005t0001g0014a0003c0005t0003g0228a0003c0005t0009g0004others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2121+1267G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215922 | ||||||
chr1:185215957
|
T | G | 1 | a0002c0002t0001g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2121+1302T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185215957 | ||||||
chr1:185215974
|
C | CT | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2121+1320dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185215974 | |||||
chr1:185216104
|
C | CT | 11 | a0003c0003t0001g0235a0003c0003t0001g0236a0003c0003t0001g0237others(8): Show | 11 | HG01099.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2121+1450dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185216104 | |||||
chr1:185216547
|
C | T | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2121+1892C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216547 | ||||||
chr1:185216561
|
A | G | 1 | a0003c0003t0001g0212 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2121+1906A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216561 | ||||||
chr1:185216687
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2032C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216687 | ||||||
chr1:185216831
|
A | T | 1 | a0001c0001t0001g0035 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2121+2176A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216831 | ||||||
chr1:185216951
|
C | CA | 17 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(14): Show | 17 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2121+2310dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185216951 | |||||
chr1:185216951
|
CA | C | 13 | a0002c0004t0001g0292a0002c0004t0001g0300a0003c0003t0001g0236others(10): Show | 13 | HG01099.hp2 HG01167.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2121+2310delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185216951 | |||||
chr1:185216966
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2311G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216966 | ||||||
chr1:185216968
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2121+2313A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185216968 | ||||||
chr1:185217017
|
T | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2362T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217017 | ||||||
chr1:185217088
|
A | G | 2 | a0003c0021t0011g0132a0015c0022t0001g0009 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2121+2433A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217088 | ||||||
chr1:185217266
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2121+2611G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217266 | ||||||
chr1:185217302
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2647C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217302 | ||||||
chr1:185217304
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2649A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217304 | ||||||
chr1:185217369
|
C | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG00140.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2121+2714C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217369 | ||||||
chr1:185217408
|
T | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2121+2753T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217408 | ||||||
chr1:185217419
|
A | G | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2121+2764A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217419 | ||||||
chr1:185217441
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2121+2786C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217441 | ||||||
chr1:185217743
|
G | A | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2121+3088G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217743 | ||||||
chr1:185217869
|
T | C | 1 | a0001c0001t0006g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2121+3214T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185217869 | ||||||
chr1:185218069
|
T | C | 1 | a0002c0002t0001g0219 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2121+3414T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185218069 | ||||||
chr1:185218265
|
G | T | 2 | a0003c0003t0001g0155a0003c0003t0001g0156 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2122-3584G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185218265 | ||||||
chr1:185218289
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2122-3560A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185218289 | ||||||
chr1:185218404
|
G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG01099.hp1 HG01256.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-3445G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185218404 | ||||||
chr1:185219576
|
T | G | 1 | a0002c0002t0001g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2122-2273T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185219576 | ||||||
chr1:185219635
|
T | C | 24 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(21): Show | 24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.2122-2214T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185219635 | ||||||
chr1:185219659
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2122-2190G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185219659 | ||||||
chr1:185219661
|
T | C | 182 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(179): Show | 184 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.2122-2188T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185219661 | ||||||
chr1:185219980
|
C | A | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2122-1869C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185219980 | ||||||
chr1:185220138
|
C | CA | 14 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0043others(11): Show | 14 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.2122-1685dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185220138 | |||||
chr1:185220138
|
CA | C | 107 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.2122-1685delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185220138 | |||||
chr1:185220138
|
CAA | C | 148 | a0001c0001t0002g0012a0001c0001t0002g0030a0001c0001t0002g0122others(145): Show | 150 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.2122-1686_2122-168 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185220138 | |||||
chr1:185220181
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2122-1668T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220181 | ||||||
chr1:185220375
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2122-1474A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220375 | ||||||
chr1:185220479
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2122-1370T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220479 | ||||||
chr1:185220610
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2122-1239T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220610 | ||||||
chr1:185220654
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0102 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2122-1195A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220654 | ||||||
chr1:185220688
|
T | C | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2122-1161T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220688 | ||||||
chr1:185220746
|
A | G | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2122-1103A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220746 | ||||||
chr1:185220949
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2122-900G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185220949 | ||||||
chr1:185221010
|
A | G | 5 | a0003c0005t0001g0014a0003c0005t0003g0228a0003c0005t0009g0004others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2122-839A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221010 | ||||||
chr1:185221040
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2122-809C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221040 | ||||||
chr1:185221050
|
G | GAC | 25 | a0001c0001t0001g0045a0001c0001t0002g0011a0001c0001t0002g0012others(22): Show | 25 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2122-766_2122-765d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221050 | |||||
chr1:185221050
|
GAC | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2122-766_2122-765d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221050 | |||||
chr1:185221050
|
GACAC | G | 21 | a0001c0001t0001g0108a0001c0001t0001g0119a0002c0002t0001g0152others(18): Show | 22 | HG00609.hp1 HG01515.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2122-768_2122-765d others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221050 | |||||
chr1:185221050
|
GACACAC | G | 139 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(136): Show | 140 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2122-770_2122-765d others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221050 | |||||
chr1:185221050
|
GACACACA others(3): Show |
G | 5 | a0002c0004t0001g0315a0003c0003t0001g0196a0003c0005t0001g0231others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.2122-774_2122-765d others(12): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221050 | |||||
chr1:185221083
|
A | T | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-766A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221083 | ||||||
chr1:185221147
|
G | T | 1 | a0003c0005t0004g0008 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2122-702G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221147 | ||||||
chr1:185221436
|
A | G | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-413A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221436 | ||||||
chr1:185221442
|
A | AT | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2122-397dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr1 | 185221442 | |||||
chr1:185221511
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2122-338G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221511 | ||||||
chr1:185221512
|
C | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2122-337C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221512 | ||||||
chr1:185221619
|
C | T | 1 | a0003c0005t0003g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2122-230C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221619 | ||||||
chr1:185221678
|
T | C | 7 | a0002c0002t0001g0188a0002c0004t0001g0316a0002c0004t0001g0317others(4): Show | 7 | NA18948.hp2 NA18967.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.2122-171T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 14/18 | chr1 | 185221678 | ||||||
chr1:185222285
|
G | T | 1 | a0001c0001t0001g0001 | 2 | HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2309+249G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222285 | ||||||
chr1:185222304
|
A | G | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2309+268A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222304 | ||||||
chr1:185222366
|
A | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0118 | 2 | HG00408.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.2309+330A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222366 | ||||||
chr1:185222483
|
G | A | 5 | a0003c0003t0001g0237a0003c0003t0001g0238a0003c0003t0001g0239others(2): Show | 5 | HG01099.hp2 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2309+447G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222483 | ||||||
chr1:185222485
|
G | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+449G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222485 | ||||||
chr1:185222514
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0107a0001c0001t0001g0124 | 3 | HG00558.hp1 HG01952.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2309+478C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222514 | ||||||
chr1:185222629
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+593A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222629 | ||||||
chr1:185222634
|
G | A | 1 | a0004c0006t0001g0153 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2309+598G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222634 | ||||||
chr1:185222638
|
A | G | 2 | a0003c0005t0001g0014a0003c0005t0003g0228 | 2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2309+602A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222638 | ||||||
chr1:185222762
|
C | CA | 54 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0031others(51): Show | 54 | HG00438.hp1 HG01106.hp2 HG01123.hp2 others(51): Show |
intron_variant | MODIFIER | c.2309+751dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185222762 | |||||
chr1:185222762
|
C | CAA | 38 | a0001c0001t0001g0108a0003c0003t0001g0190a0003c0003t0001g0191others(35): Show | 39 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2309+750_2309+751d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185222762 | |||||
chr1:185222762
|
C | CAAA | 11 | a0003c0003t0001g0193a0003c0003t0001g0194a0003c0003t0001g0195others(8): Show | 11 | HG00408.hp2 HG01106.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2309+749_2309+751d others(5): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185222762 | |||||
chr1:185222939
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+903C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222939 | ||||||
chr1:185222991
|
T | A | 186 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(183): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2309+955T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185222991 | ||||||
chr1:185223162
|
T | C | 182 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(179): Show | 184 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.2309+1126T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223162 | ||||||
chr1:185223279
|
G | A | 27 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 27 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.2309+1243G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223279 | ||||||
chr1:185223470
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0056a0001c0001t0001g0078others(1): Show | 4 | HG00140.hp2 HG00642.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+1434C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223470 | ||||||
chr1:185223471
|
G | A | 1 | a0004c0006t0001g0153 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2309+1435G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223471 | ||||||
chr1:185223722
|
G | T | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2309+1686G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223722 | ||||||
chr1:185223815
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0053others(1): Show | 4 | HG01168.hp1 HG01243.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+1779A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223815 | ||||||
chr1:185223895
|
C | T | 3 | a0001c0001t0001g0006a0003c0021t0011g0132a0015c0022t0001g0009 | 3 | HG01884.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2309+1859C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185223895 | ||||||
chr1:185224015
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+1979G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224015 | ||||||
chr1:185224322
|
G | A | 24 | a0001c0011t0001g0149a0004c0006t0001g0143a0004c0006t0001g0144others(21): Show | 24 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.2309+2286G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224322 | ||||||
chr1:185224399
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+2363A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224399 | ||||||
chr1:185224412
|
A | G | 2 | a0003c0003t0001g0263a0003c0003t0001g0264 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2309+2376A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224412 | ||||||
chr1:185224426
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2309+2390C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224426 | ||||||
chr1:185224492
|
A | AT | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2309+2465dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185224492 | |||||
chr1:185224555
|
G | A | 1 | a0003c0003t0001g0194 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2309+2519G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224555 | ||||||
chr1:185224692
|
T | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0128 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2309+2656T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224692 | ||||||
chr1:185224858
|
G | A | 6 | a0003c0005t0001g0014a0003c0005t0003g0228a0003c0005t0009g0004others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+2822G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224858 | ||||||
chr1:185224887
|
C | T | 1 | a0001c0011t0008g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2309+2851C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185224887 | ||||||
chr1:185225129
|
G | A | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+3093G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225129 | ||||||
chr1:185225239
|
C | G | 186 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(183): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2309+3203C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225239 | ||||||
chr1:185225277
|
C | G | 104 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(101): Show | 105 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(102): Show |
intron_variant | MODIFIER | c.2309+3241C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225277 | ||||||
chr1:185225467
|
A | C | 1 | a0001c0001t0001g0049 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2309+3431A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225467 | ||||||
chr1:185225548
|
T | A | 4 | a0001c0001t0001g0006a0008c0012t0001g0019a0008c0012t0001g0020others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2309+3512T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225548 | ||||||
chr1:185225668
|
G | C | 24 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(21): Show | 24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.2309+3632G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225668 | ||||||
chr1:185225832
|
A | G | 1 | a0003c0003t0001g0206 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2309+3796A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225832 | ||||||
chr1:185225909
|
C | T | 1 | a0001c0001t0002g0274 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2309+3873C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185225909 | ||||||
chr1:185226357
|
C | T | 2 | a0006c0008t0003g0244a0006c0008t0003g0245 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2309+4321C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185226357 | ||||||
chr1:185226446
|
C | T | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2309+4410C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185226446 | ||||||
chr1:185226679
|
CA | C | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+4648delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185226679 | |||||
chr1:185226732
|
CT | C | 132 | a0001c0001t0001g0129a0001c0001t0002g0274a0001c0001t0002g0278others(129): Show | 134 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(131): Show |
intron_variant | MODIFIER | c.2309+4712delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185226732 | |||||
chr1:185226732
|
CTT | C | 35 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2309+4711_2309+471 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185226732 | |||||
chr1:185226821
|
C | T | 162 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(159): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.2310-4756C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185226821 | ||||||
chr1:185226883
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2310-4694G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185226883 | ||||||
chr1:185226988
|
C | T | 1 | a0004c0006t0001g0143 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2310-4589C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185226988 | ||||||
chr1:185227201
|
A | T | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2310-4376A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227201 | ||||||
chr1:185227247
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2310-4330G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227247 | ||||||
chr1:185227429
|
A | G | 35 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2310-4148A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227429 | ||||||
chr1:185227430
|
G | A | 1 | a0003c0003t0001g0222 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2310-4147G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227430 | ||||||
chr1:185227540
|
G | A | 1 | a0006c0008t0001g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2310-4037G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227540 | ||||||
chr1:185227633
|
C | T | 9 | a0003c0005t0004g0007a0003c0005t0004g0008a0003c0005t0004g0230others(6): Show | 9 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2310-3944C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227633 | ||||||
chr1:185227634
|
G | A | 11 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2310-3943G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227634 | ||||||
chr1:185227769
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-3808G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227769 | ||||||
chr1:185227854
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-3723G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227854 | ||||||
chr1:185227869
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-3708T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185227869 | ||||||
chr1:185228016
|
G | A | 3 | a0004c0006t0001g0160a0004c0006t0001g0163a0004c0006t0001g0167 | 3 | HG01192.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2310-3561G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228016 | ||||||
chr1:185228128
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2310-3449G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228128 | ||||||
chr1:185228165
|
ATG | A | 3 | a0003c0005t0003g0228a0003c0005t0003g0252a0003c0005t0003g0255 | 3 | HG03139.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2310-3408_2310-340 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228165 | |||||
chr1:185228165
|
ATGT | A | 11 | a0003c0003t0001g0235a0003c0003t0001g0236a0003c0003t0001g0237others(8): Show | 11 | HG01099.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2310-3411_2310-340 others(7): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228165 | ||||||
chr1:185228167
|
G | GTATGTAT others(7): Show |
6 | a0001c0001t0002g0030a0001c0001t0002g0276a0001c0001t0002g0278others(3): Show | 6 | HG00438.hp1 HG03704.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.2310-3409_2310-340 others(18): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | |||||
chr1:185228167
|
G | GTATGTAT others(9): Show |
6 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0122others(3): Show | 6 | HG02071.hp2 HG02074.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.2310-3409_2310-340 others(20): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | |||||
chr1:185228167
|
G | GTATGTAT others(11): Show |
1 | a0001c0001t0002g0285 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2310-3409_2310-340 others(22): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | |||||
chr1:185228167
|
G | GTATGTAT others(13): Show |
2 | a0001c0001t0002g0277a0001c0001t0002g0281 | 2 | HG03654.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2310-3409_2310-340 others(24): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | |||||
chr1:185228167
|
G | GTATGTAT others(15): Show |
1 | a0001c0001t0002g0013 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2310-3409_2310-340 others(26): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | |||||
chr1:185228167
|
G | GTATGTAT others(17): Show |
2 | a0001c0001t0002g0280a0001c0001t0002g0283 | 2 | NA18964.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.2310-3409_2310-340 others(28): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | |||||
chr1:185228167
|
G | GTATGTAT others(19): Show |
1 | a0001c0001t0002g0282 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2310-3409_2310-340 others(30): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | |||||
chr1:185228167
|
GTGTATA | G | 75 | a0002c0002t0001g0002a0002c0002t0001g0138a0002c0002t0001g0151others(72): Show | 76 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2310-3408_2310-340 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228167 | |||||
chr1:185228169
|
G | A | 89 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(86): Show | 90 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2310-3408G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228169 | ||||||
chr1:185228169
|
G | GTA | 7 | a0001c0001t0001g0095a0001c0001t0001g0106a0001c0001t0001g0110others(4): Show | 7 | HG00735.hp1 HG01496.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2310-3389_2310-338 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228169 | |||||
chr1:185228169
|
G | GTATATAT others(3): Show |
1 | a0008c0012t0001g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2310-3397_2310-338 others(14): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228169 | |||||
chr1:185228169
|
G | GTATATAT others(5): Show |
1 | a0008c0012t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2310-3399_2310-338 others(16): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228169 | |||||
chr1:185228169
|
G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2310-3403_2310-338 others(20): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228169 | |||||
chr1:185228184
|
TATATAC | T | 11 | a0003c0003t0001g0235a0003c0003t0001g0236a0003c0003t0001g0237others(8): Show | 11 | HG01099.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2310-3387_2310-338 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228184 | |||||
chr1:185228190
|
C | T | 120 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(117): Show | 122 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.2310-3387C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228190 | ||||||
chr1:185228190
|
CATATAT | C | 3 | a0002c0002t0001g0257a0002c0002t0001g0258a0002c0002t0001g0260 | 3 | HG02572.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2310-3381_2310-337 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228190 | |||||
chr1:185228190
|
CATATATA others(1): Show |
C | 51 | a0002c0002t0001g0215a0002c0002t0001g0216a0002c0004t0001g0010others(48): Show | 51 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.2310-3383_2310-337 others(12): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228190 | |||||
chr1:185228196
|
T | C | 1 | a0002c0002t0001g0259 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2310-3381T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228196 | ||||||
chr1:185228198
|
T | C | 97 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(94): Show | 99 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(96): Show |
intron_variant | MODIFIER | c.2310-3379T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228198 | ||||||
chr1:185228198
|
T | TAC | 4 | a0003c0005t0001g0014a0003c0005t0003g0249a0003c0005t0003g0253others(1): Show | 4 | HG02055.hp2 HG02451.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310-3378_2310-337 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228198 | |||||
chr1:185228200
|
T | C | 153 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(150): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.2310-3377T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228200 | ||||||
chr1:185228200
|
T | TACAC | 3 | a0003c0005t0003g0248a0003c0005t0003g0250a0003c0005t0009g0004 | 3 | HG02109.hp2 HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2310-3375_2310-337 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228200 | |||||
chr1:185228200
|
T | TATACAC | 3 | a0003c0005t0003g0246a0003c0021t0011g0132a0015c0022t0001g0009 | 3 | HG01884.hp2 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2310-3376_2310-337 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228200 | |||||
chr1:185228200
|
T | TATATATA others(3): Show |
2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2310-3376_2310-337 others(14): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228200 | |||||
chr1:185228200
|
T | TATATATA others(7): Show |
1 | a0001c0001t0002g0275 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2310-3376_2310-337 others(18): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228200 | |||||
chr1:185228200
|
T | TATATATA others(15): Show |
1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2310-3376_2310-337 others(26): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185228200 | |||||
chr1:185228229
|
A | T | 1 | a0002c0002t0001g0221 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2310-3348A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185228229 | ||||||
chr1:185229010
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-2567G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229010 | ||||||
chr1:185229061
|
T | A | 2 | a0003c0003t0001g0271a0003c0003t0001g0272 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2310-2516T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229061 | ||||||
chr1:185229076
|
G | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-2501G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229076 | ||||||
chr1:185229228
|
G | A | 7 | a0004c0006t0001g0224a0004c0006t0001g0225a0004c0006t0001g0226others(4): Show | 7 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310-2349G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229228 | ||||||
chr1:185229494
|
T | A | 1 | a0002c0002t0001g0168 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2310-2083T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229494 | ||||||
chr1:185229659
|
T | G | 1 | a0003c0003t0001g0208 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2310-1918T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229659 | ||||||
chr1:185229735
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2310-1842G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229735 | ||||||
chr1:185229866
|
C | G | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(6): Show | 9 | HG02071.hp2 HG02074.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.2310-1711C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185229866 | ||||||
chr1:185230018
|
A | T | 35 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2310-1559A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185230018 | ||||||
chr1:185230730
|
T | TTG | 59 | a0001c0001t0001g0017a0001c0001t0002g0011a0001c0001t0002g0012others(56): Show | 59 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2310-825_2310-824d others(4): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 185230730 | |||||
chr1:185230833
|
G | A | 1 | a0003c0003t0001g0212 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2310-744G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185230833 | ||||||
chr1:185230941
|
G | T | 1 | a0003c0005t0003g0252 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2310-636G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185230941 | ||||||
chr1:185231001
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2310-576G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231001 | ||||||
chr1:185231036
|
G | A | 1 | a0002c0002t0001g0137 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2310-541G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231036 | ||||||
chr1:185231113
|
T | C | 15 | a0003c0003t0001g0235a0003c0003t0001g0236a0003c0003t0001g0237others(12): Show | 15 | HG01099.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2310-464T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231113 | ||||||
chr1:185231183
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-394A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231183 | ||||||
chr1:185231358
|
T | C | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2310-219T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231358 | ||||||
chr1:185231396
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2310-181C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231396 | ||||||
chr1:185231407
|
T | A | 1 | a0001c0001t0002g0274 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2310-170T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231407 | ||||||
chr1:185231416
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2310-161T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 15/18 | chr1 | 185231416 | ||||||
chr1:185231772
|
C | G | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2441+64C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185231772 | ||||||
chr1:185231929
|
T | C | 188 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(185): Show | 190 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.2441+221T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185231929 | ||||||
chr1:185231942
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+234C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185231942 | ||||||
chr1:185232166
|
G | A | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2441+458G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185232166 | ||||||
chr1:185232291
|
G | A | 1 | a0003c0003t0004g0233 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2441+583G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185232291 | ||||||
chr1:185232292
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+584T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185232292 | ||||||
chr1:185232979
|
C | G | 1 | a0003c0005t0003g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2441+1271C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185232979 | ||||||
chr1:185233048
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2441+1340T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233048 | ||||||
chr1:185233241
|
C | CA | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+1539dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185233241 | |||||
chr1:185233351
|
T | C | 1 | a0006c0008t0001g0141 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2441+1643T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233351 | ||||||
chr1:185233372
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+1664A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233372 | ||||||
chr1:185233709
|
T | C | 2 | a0003c0003t0001g0197a0003c0003t0001g0206 | 2 | HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2441+2001T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233709 | ||||||
chr1:185233813
|
A | G | 184 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(181): Show | 186 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.2441+2105A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233813 | ||||||
chr1:185233829
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+2121C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233829 | ||||||
chr1:185233892
|
C | T | 4 | a0001c0001t0001g0006a0008c0012t0001g0019a0008c0012t0001g0020others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2441+2184C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233892 | ||||||
chr1:185233905
|
A | G | 21 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(18): Show | 21 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2441+2197A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233905 | ||||||
chr1:185233935
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2441+2227C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233935 | ||||||
chr1:185233954
|
A | C | 3 | a0003c0003t0001g0204a0003c0003t0001g0205a0003c0003t0001g0211 | 3 | HG01106.hp1 HG01192.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.2441+2246A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185233954 | ||||||
chr1:185234060
|
G | A | 6 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2441+2352G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234060 | ||||||
chr1:185234082
|
G | A | 2 | a0003c0003t0001g0263a0003c0003t0001g0264 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2441+2374G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234082 | ||||||
chr1:185234463
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2441+2755G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234463 | ||||||
chr1:185234593
|
T | G | 61 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(58): Show | 61 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.2441+2885T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234593 | ||||||
chr1:185234708
|
G | A | 41 | a0001c0001t0004g0038a0003c0003t0001g0155a0003c0003t0001g0156others(38): Show | 41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+3000G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234708 | ||||||
chr1:185234769
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2441+3061A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185234769 | ||||||
chr1:185234901
|
T | TA | 41 | a0001c0001t0004g0038a0003c0003t0001g0155a0003c0003t0001g0156others(38): Show | 41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+3194dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185234901 | |||||
chr1:185235171
|
T | C | 7 | a0001c0001t0001g0129a0007c0010t0001g0071a0007c0010t0001g0072others(4): Show | 7 | HG01069.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2441+3463T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235171 | ||||||
chr1:185235201
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2441+3493C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235201 | ||||||
chr1:185235259
|
A | G | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2441+3551A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235259 | ||||||
chr1:185235407
|
C | T | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2441+3699C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235407 | ||||||
chr1:185235416
|
T | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0017others(294): Show | 300 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.2441+3708T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235416 | ||||||
chr1:185235422
|
A | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3714A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235422 | ||||||
chr1:185235434
|
G | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3726G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235434 | ||||||
chr1:185235437
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3729T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235437 | ||||||
chr1:185235447
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3739G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235447 | ||||||
chr1:185235452
|
A | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3744A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235452 | ||||||
chr1:185235453
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+3745G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235453 | ||||||
chr1:185235584
|
C | T | 1 | a0004c0006t0001g0147 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2441+3876C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235584 | ||||||
chr1:185235592
|
C | T | 1 | a0003c0021t0011g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2441+3884C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235592 | ||||||
chr1:185235706
|
A | G | 1 | a0001c0001t0006g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2441+3998A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235706 | ||||||
chr1:185235731
|
G | T | 1 | a0003c0003t0001g0197 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2441+4023G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235731 | ||||||
chr1:185235808
|
C | A | 3 | a0002c0002t0001g0217a0002c0002t0001g0218a0002c0002t0001g0219 | 3 | NA18961.hp2 NA19083.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2441+4100C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235808 | ||||||
chr1:185235957
|
A | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+4249A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185235957 | ||||||
chr1:185236077
|
G | A | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2441+4369G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236077 | ||||||
chr1:185236153
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2441+4445G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236153 | ||||||
chr1:185236252
|
C | CAAAAAAT | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+4552_2441+455 others(11): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185236252 | |||||
chr1:185236348
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2441+4640A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236348 | ||||||
chr1:185236356
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2441+4648G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236356 | ||||||
chr1:185236665
|
A | C | 1 | a0006c0008t0003g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2441+4957A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236665 | ||||||
chr1:185236700
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2441+4992A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236700 | ||||||
chr1:185236763
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2441+5055C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236763 | ||||||
chr1:185236842
|
T | C | 123 | a0001c0001t0007g0094a0002c0002t0001g0002a0002c0002t0001g0136others(120): Show | 125 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(122): Show |
intron_variant | MODIFIER | c.2441+5134T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236842 | ||||||
chr1:185236867
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+5159A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185236867 | ||||||
chr1:185236868
|
G | GA | 10 | a0001c0001t0004g0038a0003c0005t0004g0007a0003c0005t0004g0008others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2441+5167dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185236868 | |||||
chr1:185237003
|
A | G | 88 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(85): Show | 89 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.2441+5295A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237003 | ||||||
chr1:185237020
|
A | G | 61 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(58): Show | 61 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.2441+5312A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237020 | ||||||
chr1:185237188
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+5480A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237188 | ||||||
chr1:185237197
|
C | T | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2441+5489C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237197 | ||||||
chr1:185237235
|
T | C | 2 | a0010c0013t0001g0074a0010c0013t0001g0075 | 2 | NA18977.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2441+5527T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237235 | ||||||
chr1:185237252
|
A | G | 188 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(185): Show | 190 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.2441+5544A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237252 | ||||||
chr1:185237282
|
C | T | 15 | a0003c0003t0001g0235a0003c0003t0001g0236a0003c0003t0001g0237others(12): Show | 15 | HG01099.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2441+5574C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237282 | ||||||
chr1:185237381
|
A | T | 1 | a0006c0008t0003g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2441+5673A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237381 | ||||||
chr1:185237699
|
A | AAATAAT | 61 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(58): Show | 61 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.2441+5999_2441+600 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185237699 | |||||
chr1:185237802
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2441+6094A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185237802 | ||||||
chr1:185238009
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2441+6301C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238009 | ||||||
chr1:185238123
|
A | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0101 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2441+6415A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238123 | ||||||
chr1:185238222
|
G | A | 1 | a0007c0010t0010g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2441+6514G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238222 | ||||||
chr1:185238295
|
T | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 6 | HG00738.hp1 HG01074.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2441+6587T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238295 | ||||||
chr1:185238366
|
G | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+6658G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238366 | ||||||
chr1:185238431
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2441+6723T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238431 | ||||||
chr1:185238733
|
G | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+7025G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238733 | ||||||
chr1:185238734
|
G | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+7026G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238734 | ||||||
chr1:185238752
|
A | C | 2 | a0003c0003t0001g0155a0003c0003t0001g0156 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2441+7044A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238752 | ||||||
chr1:185238834
|
T | G | 103 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(100): Show | 104 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.2441+7126T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238834 | ||||||
chr1:185238863
|
T | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+7155T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238863 | ||||||
chr1:185238880
|
T | A | 184 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(181): Show | 186 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.2441+7172T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238880 | ||||||
chr1:185238989
|
T | C | 1 | a0006c0008t0003g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2441+7281T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185238989 | ||||||
chr1:185239056
|
G | A | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2441+7348G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239056 | ||||||
chr1:185239086
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2441+7378C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239086 | ||||||
chr1:185239088
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+7380A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239088 | ||||||
chr1:185239449
|
C | T | 103 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(100): Show | 104 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.2441+7741C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239449 | ||||||
chr1:185239505
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+7797A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239505 | ||||||
chr1:185239569
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2441+7861A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239569 | ||||||
chr1:185239607
|
C | T | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2441+7899C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239607 | ||||||
chr1:185239613
|
C | G | 1 | a0003c0005t0004g0267 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2441+7905C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239613 | ||||||
chr1:185239629
|
A | G | 24 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(21): Show | 24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.2441+7921A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185239629 | ||||||
chr1:185240099
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+8391T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240099 | ||||||
chr1:185240224
|
A | G | 1 | a0004c0006t0001g0144 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2441+8516A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240224 | ||||||
chr1:185240340
|
T | G | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2441+8632T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240340 | ||||||
chr1:185240473
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2441+8765A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240473 | ||||||
chr1:185240745
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2441+9037A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240745 | ||||||
chr1:185240898
|
A | T | 1 | a0008c0012t0001g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2441+9190A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185240898 | ||||||
chr1:185241251
|
C | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+9543C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241251 | ||||||
chr1:185241549
|
C | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+9841C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241549 | ||||||
chr1:185241625
|
C | A | 8 | a0002c0004t0001g0289a0002c0004t0001g0294a0002c0004t0001g0303others(5): Show | 8 | HG01255.hp1 HG01496.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2441+9917C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241625 | ||||||
chr1:185241656
|
C | G | 1 | a0004c0006t0001g0150 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2441+9948C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241656 | ||||||
chr1:185241741
|
T | A | 1 | a0005c0007t0001g0296 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2441+10033T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241741 | ||||||
chr1:185241881
|
A | C | 41 | a0001c0001t0004g0038a0003c0003t0001g0155a0003c0003t0001g0156others(38): Show | 41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+10173A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185241881 | ||||||
chr1:185242033
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10325C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242033 | ||||||
chr1:185242102
|
G | A | 1 | a0002c0002t0001g0173 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2441+10394G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242102 | ||||||
chr1:185242114
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10406G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242114 | ||||||
chr1:185242138
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10430C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242138 | ||||||
chr1:185242146
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2441+10438G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242146 | ||||||
chr1:185242367
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10659A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242367 | ||||||
chr1:185242402
|
G | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10694G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242402 | ||||||
chr1:185242413
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0023others(45): Show | 49 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.2441+10705A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242413 | ||||||
chr1:185242444
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10736G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242444 | ||||||
chr1:185242445
|
C | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10737C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242445 | ||||||
chr1:185242484
|
T | A | 41 | a0001c0001t0004g0038a0003c0003t0001g0155a0003c0003t0001g0156others(38): Show | 41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+10776T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242484 | ||||||
chr1:185242532
|
C | T | 1 | a0004c0006t0001g0147 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2441+10824C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242532 | ||||||
chr1:185242637
|
A | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+10929A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242637 | ||||||
chr1:185242772
|
CCTGA | C | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2441+11067_2441+11 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185242772 | |||||
chr1:185242919
|
A | G | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2441+11211A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185242919 | ||||||
chr1:185243007
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2441+11299G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243007 | ||||||
chr1:185243076
|
A | G | 41 | a0001c0001t0004g0038a0003c0003t0001g0155a0003c0003t0001g0156others(38): Show | 41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+11368A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243076 | ||||||
chr1:185243146
|
A | T | 1 | a0003c0003t0001g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2441+11438A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243146 | ||||||
chr1:185243151
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2441+11443C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243151 | ||||||
chr1:185243169
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+11461T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243169 | ||||||
chr1:185243216
|
C | G | 1 | a0003c0003t0001g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2441+11508C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243216 | ||||||
chr1:185243230
|
T | C | 1 | a0003c0003t0001g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2441+11522T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243230 | ||||||
chr1:185243237
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2441+11529T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243237 | ||||||
chr1:185243275
|
A | G | 1 | a0002c0002t0001g0169 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2441+11567A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243275 | ||||||
chr1:185243301
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+11593G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243301 | ||||||
chr1:185243354
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+11646T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243354 | ||||||
chr1:185243367
|
C | T | 1 | a0003c0003t0001g0191 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2441+11659C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243367 | ||||||
chr1:185243512
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2441+11804A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243512 | ||||||
chr1:185243547
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+11839T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243547 | ||||||
chr1:185243554
|
T | C | 186 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(183): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2441+11846T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243554 | ||||||
chr1:185243691
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0067 | 2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2441+11983A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243691 | ||||||
chr1:185243728
|
AT | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+12022delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185243728 | |||||
chr1:185243788
|
A | T | 2 | a0001c0001t0007g0094a0003c0005t0009g0004 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2441+12080A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243788 | ||||||
chr1:185243809
|
T | C | 1 | a0004c0006t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2441+12101T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243809 | ||||||
chr1:185243833
|
T | C | 41 | a0001c0001t0004g0038a0003c0003t0001g0155a0003c0003t0001g0156others(38): Show | 41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+12125T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185243833 | ||||||
chr1:185244028
|
C | T | 103 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(100): Show | 104 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.2441+12320C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244028 | ||||||
chr1:185244231
|
C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2441+12523C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244231 | ||||||
chr1:185244260
|
G | A | 1 | a0002c0004t0001g0310 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2441+12552G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244260 | ||||||
chr1:185244328
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+12620A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244328 | ||||||
chr1:185244392
|
G | A | 41 | a0001c0001t0004g0038a0003c0003t0001g0155a0003c0003t0001g0156others(38): Show | 41 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2441+12684G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244392 | ||||||
chr1:185244479
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2441+12771G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244479 | ||||||
chr1:185244631
|
A | G | 1 | a0003c0003t0001g0264 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2441+12923A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244631 | ||||||
chr1:185244806
|
C | G | 1 | a0002c0002t0001g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2441+13098C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244806 | ||||||
chr1:185244871
|
C | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13163C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244871 | ||||||
chr1:185244910
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13202G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244910 | ||||||
chr1:185244926
|
A | G | 117 | a0001c0001t0001g0031a0001c0011t0008g0261a0002c0002t0001g0002others(114): Show | 119 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(116): Show |
intron_variant | MODIFIER | c.2441+13218A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244926 | ||||||
chr1:185244930
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13222T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185244930 | ||||||
chr1:185245052
|
AG | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0077a0001c0001t0001g0128 | 3 | HG00735.hp2 HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2441+13345delG | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245052 | ||||||
chr1:185245132
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13424T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245132 | ||||||
chr1:185245380
|
T | C | 131 | a0001c0001t0007g0094a0002c0002t0001g0002a0002c0002t0001g0136others(128): Show | 133 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(130): Show |
intron_variant | MODIFIER | c.2441+13672T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245380 | ||||||
chr1:185245394
|
G | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13686G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245394 | ||||||
chr1:185245396
|
G | A | 1 | a0003c0003t0001g0190 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2441+13688G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245396 | ||||||
chr1:185245482
|
G | C | 1 | a0003c0003t0001g0198 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2441+13774G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245482 | ||||||
chr1:185245593
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+13885G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245593 | ||||||
chr1:185245624
|
G | A | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2441+13916G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245624 | ||||||
chr1:185245638
|
C | T | 2 | a0006c0008t0001g0140a0006c0008t0001g0142 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2441+13930C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245638 | ||||||
chr1:185245710
|
T | A | 3 | a0003c0005t0004g0007a0003c0005t0004g0008a0003c0005t0004g0230 | 3 | HG01891.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2441+14002T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245710 | ||||||
chr1:185245737
|
A | AT | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+14036dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185245737 | |||||
chr1:185245820
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2441+14112G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245820 | ||||||
chr1:185245821
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2441+14113C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245821 | ||||||
chr1:185245837
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+14129C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185245837 | ||||||
chr1:185246048
|
G | A | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2441+14340G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185246048 | ||||||
chr1:185246347
|
G | A | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2441+14639G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185246347 | ||||||
chr1:185246357
|
G | A | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2441+14649G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185246357 | ||||||
chr1:185246623
|
C | CT | 33 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0051others(30): Show | 34 | HG01243.hp1 HG02040.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.2441+14936dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185246623 | |||||
chr1:185246623
|
C | CTT | 33 | a0001c0001t0004g0038a0002c0002t0001g0219a0003c0003t0001g0191others(30): Show | 33 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.2441+14935_2441+14 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185246623 | |||||
chr1:185246623
|
C | CTTT | 91 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(88): Show | 92 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.2441+14934_2441+14 others(9): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185246623 | |||||
chr1:185246623
|
C | CTTTT | 32 | a0002c0002t0001g0138a0002c0002t0001g0175a0002c0002t0001g0188others(29): Show | 32 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.2441+14933_2441+14 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185246623 | |||||
chr1:185246623
|
CT | C | 8 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0001g0091others(5): Show | 8 | HG01070.hp2 HG01256.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2441+14936delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185246623 | |||||
chr1:185246822
|
T | A | 1 | a0003c0003t0001g0220 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2441+15114T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185246822 | ||||||
chr1:185247038
|
C | T | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2441+15330C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185247038 | ||||||
chr1:185247128
|
A | G | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2441+15420A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185247128 | ||||||
chr1:185247179
|
G | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0127 | 2 | NA18943.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.2441+15471G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185247179 | ||||||
chr1:185247648
|
C | T | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2441+15940C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185247648 | ||||||
chr1:185247696
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+15988T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185247696 | ||||||
chr1:185248035
|
T | A | 14 | a0003c0005t0003g0003a0003c0005t0003g0228a0003c0005t0003g0246others(11): Show | 15 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2441+16327T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185248035 | ||||||
chr1:185248284
|
AAAC | A | 14 | a0003c0005t0003g0003a0003c0005t0003g0228a0003c0005t0003g0246others(11): Show | 15 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2441+16579_2441+16 others(9): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185248284 | |||||
chr1:185248352
|
A | G | 2 | a0006c0008t0003g0244a0006c0008t0003g0245 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2441+16644A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185248352 | ||||||
chr1:185248606
|
G | A | 8 | a0002c0004t0001g0289a0002c0004t0001g0294a0002c0004t0001g0303others(5): Show | 8 | HG01255.hp1 HG01496.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2441+16898G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185248606 | ||||||
chr1:185248775
|
C | CA | 7 | a0001c0001t0001g0006a0001c0001t0001g0112a0001c0001t0001g0129others(4): Show | 7 | HG02109.hp1 HG02132.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2441+17085dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185248775 | |||||
chr1:185248775
|
CA | C | 26 | a0001c0001t0001g0026a0001c0001t0001g0053a0001c0001t0001g0063others(23): Show | 26 | HG00438.hp1 HG01975.hp2 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.2441+17085delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185248775 | |||||
chr1:185248775
|
CAA | C | 120 | a0001c0001t0007g0094a0002c0002t0001g0002a0002c0002t0001g0136others(117): Show | 122 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(119): Show |
intron_variant | MODIFIER | c.2441+17084_2441+17 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185248775 | |||||
chr1:185248775
|
CAAA | C | 10 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(7): Show | 10 | HG02258.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2441+17083_2441+17 others(9): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185248775 | |||||
chr1:185248860
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2441+17152A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185248860 | ||||||
chr1:185249049
|
G | A | 1 | a0001c0011t0008g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2441+17341G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185249049 | ||||||
chr1:185249551
|
C | T | 2 | a0006c0008t0003g0244a0006c0008t0003g0245 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2441+17843C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185249551 | ||||||
chr1:185249774
|
G | T | 1 | a0002c0004t0001g0297 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2441+18066G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185249774 | ||||||
chr1:185249876
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2441+18168C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185249876 | ||||||
chr1:185250007
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+18299A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250007 | ||||||
chr1:185250103
|
T | C | 6 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2441+18395T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250103 | ||||||
chr1:185250152
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2441+18444G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250152 | ||||||
chr1:185250164
|
G | A | 185 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(182): Show | 187 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.2441+18456G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250164 | ||||||
chr1:185250238
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0017others(294): Show | 300 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.2441+18530T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250238 | ||||||
chr1:185250415
|
T | A | 1 | a0005c0007t0001g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2441+18707T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250415 | ||||||
chr1:185250528
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2441+18820C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250528 | ||||||
chr1:185250530
|
C | A | 1 | a0001c0001t0002g0275 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2441+18822C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250530 | ||||||
chr1:185250548
|
C | T | 170 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(167): Show | 171 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.2441+18840C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250548 | ||||||
chr1:185250622
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2441+18914C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250622 | ||||||
chr1:185250642
|
TATTTAAT others(4): Show |
T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2441+18935_2441+18 others(17): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250642 | ||||||
chr1:185250668
|
A | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00597.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.2441+18960A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250668 | ||||||
chr1:185250749
|
A | G | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2441+19041A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250749 | ||||||
chr1:185250756
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2441+19048G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250756 | ||||||
chr1:185250811
|
C | T | 1 | a0003c0021t0011g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2441+19103C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250811 | ||||||
chr1:185250860
|
G | A | 105 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(102): Show | 106 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(103): Show |
intron_variant | MODIFIER | c.2441+19152G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250860 | ||||||
chr1:185250950
|
A | G | 24 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0033others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2441+19242A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250950 | ||||||
chr1:185250955
|
A | G | 186 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(183): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2441+19247A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185250955 | ||||||
chr1:185251553
|
T | C | 1 | a0002c0002t0001g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2442-19770T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251553 | ||||||
chr1:185251797
|
TA | T | 5 | a0002c0002t0001g0170a0003c0003t0001g0155a0003c0003t0001g0156others(2): Show | 5 | HG01361.hp2 HG02559.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2442-19525delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251797 | ||||||
chr1:185251798
|
A | T | 58 | a0001c0001t0004g0038a0002c0004t0001g0304a0002c0004t0001g0311others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.2442-19525A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251798 | ||||||
chr1:185251800
|
T | A | 2 | a0001c0001t0001g0103a0002c0002t0001g0154 | 2 | HG02896.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.2442-19523T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251800 | ||||||
chr1:185251838
|
C | T | 1 | a0002c0002t0001g0182 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2442-19485C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251838 | ||||||
chr1:185251863
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2442-19460A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185251863 | ||||||
chr1:185252014
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0080a0001c0011t0001g0149 | 3 | HG01106.hp2 NA18954.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2442-19309A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252014 | ||||||
chr1:185252092
|
A | T | 5 | a0004c0006t0001g0224a0004c0006t0001g0225a0004c0006t0001g0226others(2): Show | 5 | HG02630.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2442-19231A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252092 | ||||||
chr1:185252116
|
A | T | 90 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(87): Show | 91 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.2442-19207A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252116 | ||||||
chr1:185252184
|
G | T | 1 | a0001c0001t0002g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2442-19139G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252184 | ||||||
chr1:185252230
|
T | C | 55 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(52): Show | 55 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2442-19093T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252230 | ||||||
chr1:185252231
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-19092G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252231 | ||||||
chr1:185252243
|
C | T | 1 | a0005c0007t0001g0305 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2442-19080C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252243 | ||||||
chr1:185252351
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2442-18972T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252351 | ||||||
chr1:185252352
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2442-18971G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252352 | ||||||
chr1:185252676
|
A | G | 1 | a0003c0021t0011g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2442-18647A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252676 | ||||||
chr1:185252696
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2442-18627G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252696 | ||||||
chr1:185252794
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0277 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2442-18529C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252794 | ||||||
chr1:185252860
|
G | A | 1 | a0003c0005t0003g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2442-18463G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252860 | ||||||
chr1:185252861
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2442-18462C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252861 | ||||||
chr1:185252899
|
G | C | 16 | a0003c0005t0001g0231a0003c0005t0001g0232a0003c0005t0003g0003others(13): Show | 17 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2442-18424G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252899 | ||||||
chr1:185252923
|
G | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0277 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2442-18400G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252923 | ||||||
chr1:185252957
|
G | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0080a0001c0011t0001g0149 | 3 | HG01106.hp2 NA18954.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2442-18366G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252957 | ||||||
chr1:185252963
|
G | T | 1 | a0005c0007t0001g0323 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2442-18360G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185252963 | ||||||
chr1:185253010
|
G | T | 19 | a0001c0001t0007g0094a0003c0005t0001g0231a0003c0005t0001g0232others(16): Show | 20 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2442-18313G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253010 | ||||||
chr1:185253037
|
G | A | 1 | a0004c0006t0001g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2442-18286G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253037 | ||||||
chr1:185253069
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2442-18254G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253069 | ||||||
chr1:185253142
|
A | G | 1 | a0003c0021t0011g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2442-18181A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253142 | ||||||
chr1:185253264
|
A | G | 190 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(187): Show | 192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2442-18059A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253264 | ||||||
chr1:185253443
|
T | C | 1 | a0002c0002t0001g0170 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2442-17880T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253443 | ||||||
chr1:185253466
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2442-17857T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253466 | ||||||
chr1:185253497
|
A | G | 1 | a0002c0004t0001g0308 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2442-17826A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253497 | ||||||
chr1:185253559
|
T | A | 27 | a0002c0002t0001g0002a0002c0002t0001g0151a0002c0002t0001g0168others(24): Show | 28 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.2442-17764T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253559 | ||||||
chr1:185253583
|
T | TTGTC | 55 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(52): Show | 55 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2442-17737_2442-17 others(10): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185253583 | |||||
chr1:185253677
|
C | G | 1 | a0003c0003t0001g0212 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2442-17646C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253677 | ||||||
chr1:185253677
|
C | T | 5 | a0004c0006t0001g0224a0004c0006t0001g0225a0004c0006t0001g0226others(2): Show | 5 | HG02630.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2442-17646C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253677 | ||||||
chr1:185253742
|
T | TC | 55 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(52): Show | 55 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2442-17580dupC | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185253742 | |||||
chr1:185253785
|
A | G | 1 | a0003c0005t0004g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2442-17538A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253785 | ||||||
chr1:185253858
|
A | G | 37 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(34): Show | 37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2442-17465A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253858 | ||||||
chr1:185253894
|
A | G | 105 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(102): Show | 106 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(103): Show |
intron_variant | MODIFIER | c.2442-17429A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253894 | ||||||
chr1:185253925
|
T | C | 16 | a0003c0005t0001g0231a0003c0005t0001g0232a0003c0005t0003g0003others(13): Show | 17 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2442-17398T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185253925 | ||||||
chr1:185254057
|
C | T | 1 | a0003c0003t0001g0240 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2442-17266C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254057 | ||||||
chr1:185254093
|
G | A | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-17230G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254093 | ||||||
chr1:185254174
|
G | A | 2 | a0002c0002t0001g0136a0002c0002t0001g0137 | 2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2442-17149G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254174 | ||||||
chr1:185254175
|
T | G | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2442-17148T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254175 | ||||||
chr1:185254191
|
T | C | 1 | a0002c0002t0001g0178 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2442-17132T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254191 | ||||||
chr1:185254247
|
T | G | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2442-17076T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254247 | ||||||
chr1:185254392
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-16931G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254392 | ||||||
chr1:185254398
|
C | G | 322 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(319): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.2442-16925C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254398 | ||||||
chr1:185254404
|
G | T | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-16919G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254404 | ||||||
chr1:185254415
|
CCT | C | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-16907_2442-16 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254415 | ||||||
chr1:185254416
|
C | T | 186 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(183): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2442-16907C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254416 | ||||||
chr1:185254638
|
T | C | 1 | a0005c0007t0001g0298 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2442-16685T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254638 | ||||||
chr1:185254666
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-16657T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254666 | ||||||
chr1:185254680
|
A | G | 4 | a0004c0009t0001g0061a0004c0009t0001g0130a0009c0017t0001g0076others(1): Show | 4 | HG00280.hp2 HG00639.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-16643A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254680 | ||||||
chr1:185254771
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0017others(257): Show | 263 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.2442-16552C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254771 | ||||||
chr1:185254892
|
T | C | 24 | a0004c0006t0001g0143a0004c0006t0001g0144a0004c0006t0001g0145others(21): Show | 24 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2442-16431T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185254892 | ||||||
chr1:185255030
|
G | A | 1 | a0003c0021t0011g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2442-16293G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255030 | ||||||
chr1:185255243
|
A | G | 1 | a0008c0012t0001g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2442-16080A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255243 | ||||||
chr1:185255387
|
A | G | 190 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(187): Show | 192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2442-15936A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255387 | ||||||
chr1:185255394
|
A | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0006g0126 | 3 | HG00597.hp2 NA18943.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.2442-15929A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255394 | ||||||
chr1:185255435
|
C | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0097 | 3 | HG00438.hp2 HG02056.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.2442-15888C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255435 | ||||||
chr1:185255457
|
G | T | 1 | a0002c0002t0001g0186 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2442-15866G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255457 | ||||||
chr1:185255681
|
C | T | 190 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(187): Show | 192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2442-15642C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255681 | ||||||
chr1:185255780
|
G | A | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2442-15543G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255780 | ||||||
chr1:185255813
|
C | A | 2 | a0002c0002t0001g0175a0002c0002t0001g0214 | 2 | HG01175.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2442-15510C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255813 | ||||||
chr1:185255868
|
C | G | 5 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(2): Show | 6 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-15455C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255868 | ||||||
chr1:185255871
|
A | G | 1 | a0005c0007t0001g0305 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2442-15452A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255871 | ||||||
chr1:185255876
|
T | C | 6 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(3): Show | 7 | HG02647.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2442-15447T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255876 | ||||||
chr1:185255881
|
G | T | 5 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(2): Show | 6 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-15442G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255881 | ||||||
chr1:185255883
|
C | G | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2442-15440C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255883 | ||||||
chr1:185255928
|
G | C | 55 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(52): Show | 55 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2442-15395G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255928 | ||||||
chr1:185255935
|
T | C | 1 | a0002c0002t0001g0170 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2442-15388T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255935 | ||||||
chr1:185255979
|
A | G | 1 | a0003c0003t0001g0202 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2442-15344A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185255979 | ||||||
chr1:185256032
|
G | A | 1 | a0003c0005t0001g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2442-15291G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256032 | ||||||
chr1:185256107
|
C | A | 105 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(102): Show | 106 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(103): Show |
intron_variant | MODIFIER | c.2442-15216C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256107 | ||||||
chr1:185256109
|
C | A | 1 | a0003c0005t0003g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2442-15214C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256109 | ||||||
chr1:185256140
|
C | T | 1 | a0002c0002t0001g0219 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2442-15183C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256140 | ||||||
chr1:185256146
|
A | T | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-15177A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256146 | ||||||
chr1:185256149
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0099 | 2 | HG02080.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.2442-15174C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256149 | ||||||
chr1:185256210
|
A | T | 15 | a0003c0003t0001g0235a0003c0003t0001g0236a0003c0003t0001g0237others(12): Show | 15 | HG01099.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2442-15113A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256210 | ||||||
chr1:185256227
|
T | C | 1 | a0003c0005t0001g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2442-15096T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256227 | ||||||
chr1:185256232
|
G | C | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2442-15091G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256232 | ||||||
chr1:185256508
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0277 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2442-14815C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256508 | ||||||
chr1:185256511
|
C | T | 1 | a0004c0006t0001g0164 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2442-14812C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256511 | ||||||
chr1:185256527
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2442-14796C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256527 | ||||||
chr1:185256530
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2442-14793T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256530 | ||||||
chr1:185256568
|
C | T | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2442-14755C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256568 | ||||||
chr1:185256569
|
G | A | 1 | a0002c0002t0001g0185 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2442-14754G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256569 | ||||||
chr1:185256573
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0017others(294): Show | 300 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.2442-14750T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256573 | ||||||
chr1:185256600
|
C | T | 2 | a0002c0004t0001g0010a0002c0004t0001g0292 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2442-14723C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256600 | ||||||
chr1:185256694
|
CA | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-14626delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185256694 | |||||
chr1:185256736
|
G | C | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-14587G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256736 | ||||||
chr1:185256766
|
G | C | 186 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(183): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2442-14557G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256766 | ||||||
chr1:185256905
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2442-14418T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256905 | ||||||
chr1:185256946
|
C | T | 22 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(19): Show | 22 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.2442-14377C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185256946 | ||||||
chr1:185257016
|
T | G | 1 | a0002c0004t0001g0302 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2442-14307T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257016 | ||||||
chr1:185257022
|
G | C | 1 | a0002c0004t0001g0302 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2442-14301G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257022 | ||||||
chr1:185257030
|
A | C | 1 | a0003c0005t0003g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2442-14293A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257030 | ||||||
chr1:185257038
|
C | T | 4 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(1): Show | 4 | HG02559.hp1 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-14285C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257038 | ||||||
chr1:185257039
|
C | T | 1 | a0013c0016t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2442-14284C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257039 | ||||||
chr1:185257049
|
G | A | 1 | a0002c0004t0001g0302 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2442-14274G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257049 | ||||||
chr1:185257103
|
T | G | 4 | a0002c0002t0001g0172a0002c0002t0001g0273a0002c0004t0001g0302others(1): Show | 4 | HG03486.hp1 HG03704.hp1 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.2442-14220T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257103 | ||||||
chr1:185257109
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0005g0100 | 2 | HG00140.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2442-14214G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257109 | ||||||
chr1:185257136
|
G | A | 2 | a0001c0001t0001g0031a0003c0005t0001g0014 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2442-14187G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257136 | ||||||
chr1:185257143
|
T | G | 2 | a0002c0002t0001g0172a0002c0002t0001g0273 | 2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2442-14180T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257143 | ||||||
chr1:185257221
|
C | T | 4 | a0001c0001t0001g0006a0008c0012t0001g0019a0008c0012t0001g0020others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2442-14102C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257221 | ||||||
chr1:185257247
|
C | G | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-14076C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257247 | ||||||
chr1:185257319
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2442-14004C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257319 | ||||||
chr1:185257324
|
T | C | 5 | a0001c0001t0007g0094a0002c0002t0001g0287a0002c0002t0001g0288others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2442-13999T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257324 | ||||||
chr1:185257338
|
A | G | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-13985A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257338 | ||||||
chr1:185257352
|
G | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0277 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2442-13971G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257352 | ||||||
chr1:185257357
|
A | G | 2 | a0002c0002t0001g0138a0002c0002t0001g0154 | 2 | HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2442-13966A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257357 | ||||||
chr1:185257361
|
A | C | 1 | a0004c0006t0001g0227 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2442-13962A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257361 | ||||||
chr1:185257384
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0052 | 2 | NA18962.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2442-13939C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257384 | ||||||
chr1:185257410
|
C | G | 105 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(102): Show | 106 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(103): Show |
intron_variant | MODIFIER | c.2442-13913C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257410 | ||||||
chr1:185257502
|
G | C | 131 | a0001c0001t0007g0094a0002c0002t0001g0002a0002c0002t0001g0136others(128): Show | 133 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(130): Show |
intron_variant | MODIFIER | c.2442-13821G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257502 | ||||||
chr1:185257506
|
G | A | 2 | a0003c0005t0001g0014a0003c0005t0004g0267 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2442-13817G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257506 | ||||||
chr1:185257513
|
C | T | 2 | a0006c0008t0003g0244a0006c0008t0003g0245 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2442-13810C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257513 | ||||||
chr1:185257555
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2442-13768T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257555 | ||||||
chr1:185257561
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2442-13762C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257561 | ||||||
chr1:185257601
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2442-13722C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257601 | ||||||
chr1:185257619
|
A | G | 190 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(187): Show | 192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2442-13704A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257619 | ||||||
chr1:185257635
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2442-13688C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257635 | ||||||
chr1:185257683
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0037 | 3 | HG02145.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2442-13640C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257683 | ||||||
chr1:185257705
|
G | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-13618G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257705 | ||||||
chr1:185257706
|
G | T | 131 | a0001c0001t0007g0094a0002c0002t0001g0002a0002c0002t0001g0136others(128): Show | 133 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(130): Show |
intron_variant | MODIFIER | c.2442-13617G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257706 | ||||||
chr1:185257734
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-13589C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257734 | ||||||
chr1:185257770
|
A | G | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-13553A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257770 | ||||||
chr1:185257785
|
C | T | 16 | a0003c0005t0001g0231a0003c0005t0001g0232a0003c0005t0003g0003others(13): Show | 17 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2442-13538C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257785 | ||||||
chr1:185257932
|
A | G | 1 | a0003c0021t0011g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2442-13391A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185257932 | ||||||
chr1:185258019
|
C | G | 4 | a0001c0001t0001g0006a0008c0012t0001g0019a0008c0012t0001g0020others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2442-13304C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258019 | ||||||
chr1:185258272
|
C | T | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-13051C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258272 | ||||||
chr1:185258281
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0277 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2442-13042C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258281 | ||||||
chr1:185258394
|
A | G | 2 | a0003c0003t0001g0193a0003c0003t0001g0194 | 2 | HG00408.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.2442-12929A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258394 | ||||||
chr1:185258405
|
T | C | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-12918T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258405 | ||||||
chr1:185258510
|
A | C | 15 | a0003c0003t0001g0235a0003c0003t0001g0236a0003c0003t0001g0237others(12): Show | 15 | HG01099.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2442-12813A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258510 | ||||||
chr1:185258520
|
T | G | 1 | a0002c0002t0001g0138 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2442-12803T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258520 | ||||||
chr1:185258679
|
A | G | 1 | a0002c0002t0001g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2442-12644A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258679 | ||||||
chr1:185258754
|
G | A | 186 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(183): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2442-12569G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258754 | ||||||
chr1:185258766
|
C | G | 6 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-12557C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258766 | ||||||
chr1:185258778
|
A | G | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-12545A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258778 | ||||||
chr1:185258845
|
A | C | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-12478A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185258845 | ||||||
chr1:185259114
|
C | A | 1 | a0002c0004t0001g0294 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2442-12209C>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259114 | ||||||
chr1:185259304
|
C | T | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-12019C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259304 | ||||||
chr1:185259786
|
T | C | 1 | a0003c0005t0003g0252 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2442-11537T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259786 | ||||||
chr1:185259821
|
A | G | 1 | a0003c0003t0001g0205 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2442-11502A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259821 | ||||||
chr1:185259833
|
A | G | 1 | a0003c0003t0001g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2442-11490A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259833 | ||||||
chr1:185259866
|
T | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0014c0015t0001g0090 | 3 | HG00621.hp2 HG01952.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2442-11457T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185259866 | ||||||
chr1:185260153
|
G | A | 10 | a0001c0001t0004g0038a0003c0005t0004g0007a0003c0005t0004g0008others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2442-11170G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185260153 | ||||||
chr1:185260349
|
C | T | 25 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(22): Show | 25 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.2442-10974C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185260349 | ||||||
chr1:185260669
|
T | C | 186 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(183): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2442-10654T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185260669 | ||||||
chr1:185260792
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-10531C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185260792 | ||||||
chr1:185261065
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-10258T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261065 | ||||||
chr1:185261519
|
G | A | 2 | a0003c0003t0001g0271a0003c0003t0001g0272 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2442-9804G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261519 | ||||||
chr1:185261533
|
C | T | 1 | a0010c0013t0001g0075 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2442-9790C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261533 | ||||||
chr1:185261535
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2442-9788T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261535 | ||||||
chr1:185261541
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0055 | 2 | HG02165.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2442-9782A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261541 | ||||||
chr1:185261569
|
A | G | 2 | a0002c0002t0001g0215a0002c0002t0001g0216 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2442-9754A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261569 | ||||||
chr1:185261673
|
CTT | C | 143 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(140): Show | 145 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.2442-9636_2442-963 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185261673 | |||||
chr1:185261673
|
CTTT | C | 67 | a0002c0002t0001g0188a0002c0002t0001g0215a0002c0002t0001g0216others(64): Show | 67 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2442-9637_2442-963 others(7): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185261673 | |||||
chr1:185261718
|
G | T | 155 | a0001c0001t0007g0094a0002c0002t0001g0002a0002c0002t0001g0136others(152): Show | 157 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.2442-9605G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261718 | ||||||
chr1:185261934
|
G | A | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2442-9389G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261934 | ||||||
chr1:185261970
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2442-9353A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185261970 | ||||||
chr1:185262007
|
G | A | 7 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2442-9316G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262007 | ||||||
chr1:185262066
|
C | T | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2442-9257C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262066 | ||||||
chr1:185262183
|
G | A | 10 | a0002c0004t0001g0289a0002c0004t0001g0294a0002c0004t0001g0303others(7): Show | 10 | HG01255.hp1 HG01496.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.2442-9140G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262183 | ||||||
chr1:185262190
|
T | G | 1 | a0015c0022t0001g0009 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2442-9133T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262190 | ||||||
chr1:185262386
|
C | T | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-8937C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262386 | ||||||
chr1:185262440
|
C | T | 10 | a0001c0001t0004g0038a0003c0005t0004g0007a0003c0005t0004g0008others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2442-8883C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262440 | ||||||
chr1:185262514
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2442-8809C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262514 | ||||||
chr1:185262786
|
C | CT | 27 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0007g0094others(24): Show | 27 | HG00735.hp1 HG01099.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.2442-8520dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185262786 | |||||
chr1:185262786
|
CT | C | 9 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0089others(6): Show | 9 | HG01069.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.2442-8520delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185262786 | |||||
chr1:185262810
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2442-8513G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262810 | ||||||
chr1:185262855
|
T | C | 210 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(207): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2442-8468T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262855 | ||||||
chr1:185262894
|
T | A | 1 | a0004c0006t0001g0148 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2442-8429T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262894 | ||||||
chr1:185262933
|
G | A | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-8390G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185262933 | ||||||
chr1:185263024
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-8299T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185263024 | ||||||
chr1:185263042
|
C | T | 12 | a0003c0005t0003g0003a0003c0005t0003g0228a0003c0005t0003g0246others(9): Show | 13 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.2442-8281C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185263042 | ||||||
chr1:185263119
|
G | A | 155 | a0001c0001t0007g0094a0002c0002t0001g0002a0002c0002t0001g0136others(152): Show | 157 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.2442-8204G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185263119 | ||||||
chr1:185263284
|
C | CA | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-8029dupA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185263284 | |||||
chr1:185263372
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2442-7951T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185263372 | ||||||
chr1:185263403
|
C | T | 6 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-7920C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185263403 | ||||||
chr1:185264132
|
T | C | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2442-7191T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185264132 | ||||||
chr1:185264183
|
G | A | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2442-7140G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185264183 | ||||||
chr1:185264227
|
G | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2442-7096G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185264227 | ||||||
chr1:185264253
|
T | C | 1 | a0015c0022t0001g0009 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2442-7070T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185264253 | ||||||
chr1:185264338
|
C | T | 25 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(22): Show | 25 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.2442-6985C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185264338 | ||||||
chr1:185265108
|
C | T | 1 | a0002c0002t0001g0188 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2442-6215C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265108 | ||||||
chr1:185265284
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2442-6039A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265284 | ||||||
chr1:185265351
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2442-5972A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265351 | ||||||
chr1:185265411
|
T | C | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-5912T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265411 | ||||||
chr1:185265541
|
C | T | 1 | a0002c0002t0001g0260 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2442-5782C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265541 | ||||||
chr1:185265580
|
C | T | 1 | a0001c0001t0006g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2442-5743C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265580 | ||||||
chr1:185265597
|
A | G | 1 | a0003c0005t0004g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2442-5726A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185265597 | ||||||
chr1:185266156
|
C | G | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2442-5167C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266156 | ||||||
chr1:185266212
|
C | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0011t0001g0149 | 3 | HG01123.hp2 NA18954.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2442-5111C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266212 | ||||||
chr1:185266213
|
G | A | 1 | a0004c0006t0001g0163 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2442-5110G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266213 | ||||||
chr1:185266230
|
AT | A | 45 | a0002c0002t0001g0002a0002c0002t0001g0136a0002c0002t0001g0137others(42): Show | 46 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2442-5086delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185266230 | |||||
chr1:185266265
|
C | T | 2 | a0001c0001t0001g0045a0012c0018t0001g0029 | 2 | HG01069.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2442-5058C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266265 | ||||||
chr1:185266403
|
T | G | 14 | a0003c0005t0003g0003a0003c0005t0003g0228a0003c0005t0003g0246others(11): Show | 15 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2442-4920T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266403 | ||||||
chr1:185266908
|
G | T | 1 | a0002c0002t0001g0002 | 2 | HG00639.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2442-4415G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185266908 | ||||||
chr1:185267027
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2442-4296G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267027 | ||||||
chr1:185267033
|
G | A | 21 | a0002c0002t0001g0188a0002c0004t0001g0027a0002c0004t0001g0028others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.2442-4290G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267033 | ||||||
chr1:185267045
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2442-4278T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267045 | ||||||
chr1:185267083
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2442-4240G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267083 | ||||||
chr1:185267257
|
C | T | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2442-4066C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267257 | ||||||
chr1:185267352
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2442-3971C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267352 | ||||||
chr1:185267380
|
G | A | 210 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(207): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2442-3943G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267380 | ||||||
chr1:185267467
|
A | G | 2 | a0006c0008t0001g0140a0006c0008t0001g0142 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2442-3856A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267467 | ||||||
chr1:185267649
|
T | C | 1 | a0002c0002t0001g0188 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2442-3674T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267649 | ||||||
chr1:185267798
|
G | T | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2442-3525G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185267798 | ||||||
chr1:185268505
|
A | G | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-2818A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185268505 | ||||||
chr1:185268757
|
C | G | 1 | a0001c0001t0001g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2442-2566C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185268757 | ||||||
chr1:185268853
|
C | CT | 58 | a0001c0001t0001g0088a0002c0002t0001g0002a0002c0002t0001g0151others(55): Show | 59 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.2442-2453dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185268853 | |||||
chr1:185268853
|
CT | C | 6 | a0001c0001t0001g0069a0001c0001t0001g0119a0001c0001t0001g0120others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-2453delT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185268853 | |||||
chr1:185268875
|
C | T | 1 | a0003c0005t0009g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2442-2448C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185268875 | ||||||
chr1:185268892
|
G | A | 1 | a0006c0008t0001g0189 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2442-2431G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185268892 | ||||||
chr1:185268937
|
C | G | 6 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442-2386C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185268937 | ||||||
chr1:185269001
|
C | T | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2442-2322C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269001 | ||||||
chr1:185269069
|
G | T | 156 | a0001c0001t0001g0102a0001c0001t0007g0094a0002c0002t0001g0002others(153): Show | 158 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(155): Show |
intron_variant | MODIFIER | c.2442-2254G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269069 | ||||||
chr1:185269074
|
G | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG01099.hp1 HG01256.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-2249G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269074 | ||||||
chr1:185269075
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2442-2248A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269075 | ||||||
chr1:185269084
|
C | T | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2442-2239C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269084 | ||||||
chr1:185269141
|
C | T | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2442-2182C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269141 | ||||||
chr1:185269147
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2442-2176T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269147 | ||||||
chr1:185269335
|
T | C | 1 | a0003c0003t0001g0190 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2442-1988T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269335 | ||||||
chr1:185269367
|
G | GT | 10 | a0001c0001t0004g0038a0003c0005t0004g0007a0003c0005t0004g0008others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2442-1951dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185269367 | |||||
chr1:185269367
|
G | GTTT | 20 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0193others(17): Show | 20 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.2442-1953_2442-195 others(7): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185269367 | |||||
chr1:185269373
|
G | GT | 55 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0031others(52): Show | 56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.2442-1935dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185269373 | |||||
chr1:185269373
|
G | T | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-1950G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269373 | ||||||
chr1:185269379
|
T | G | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2442-1944T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269379 | ||||||
chr1:185269380
|
T | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0089 | 2 | HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2442-1943T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269380 | ||||||
chr1:185269456
|
T | C | 4 | a0002c0002t0001g0257a0002c0002t0001g0258a0002c0002t0001g0259others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-1867T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269456 | ||||||
chr1:185269516
|
A | G | 2 | a0003c0005t0001g0014a0011c0020t0001g0131 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2442-1807A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269516 | ||||||
chr1:185269537
|
G | A | 210 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(207): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2442-1786G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269537 | ||||||
chr1:185269943
|
T | A | 1 | a0003c0005t0004g0267 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2442-1380T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185269943 | ||||||
chr1:185270034
|
T | A | 3 | a0004c0006t0001g0143a0004c0006t0001g0144a0004c0006t0001g0145 | 3 | HG00738.hp2 HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2442-1289T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270034 | ||||||
chr1:185270265
|
A | G | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-1058A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270265 | ||||||
chr1:185270302
|
T | C | 4 | a0001c0001t0007g0094a0003c0005t0003g0252a0003c0005t0003g0255others(1): Show | 4 | HG01257.hp2 HG03486.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442-1021T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270302 | ||||||
chr1:185270302
|
T | TC | 203 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(200): Show | 205 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.2442-1019dupC | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 185270302 | |||||
chr1:185270358
|
A | C | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2442-965A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270358 | ||||||
chr1:185270566
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2442-757G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270566 | ||||||
chr1:185270663
|
C | T | 209 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(206): Show | 211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.2442-660C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270663 | ||||||
chr1:185270697
|
A | G | 1 | a0002c0004t0001g0320 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2442-626A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185270697 | ||||||
chr1:185271018
|
T | A | 2 | a0002c0004t0001g0010a0002c0004t0001g0292 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2442-305T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185271018 | ||||||
chr1:185271044
|
A | T | 1 | a0003c0005t0004g0268 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2442-279A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185271044 | ||||||
chr1:185271268
|
T | C | 5 | a0007c0010t0001g0071a0007c0010t0001g0072a0007c0010t0001g0073others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2442-55T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 16/18 | chr1 | 185271268 | ||||||
chr1:185271439
|
T | G | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2508+50T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185271439 | ||||||
chr1:185271513
|
T | C | 1 | a0004c0009t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2508+124T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185271513 | ||||||
chr1:185271530
|
T | TTGTCAGT others(12): Show |
1 | a0001c0001t0001g0016 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2508+152_2508+153i others(21): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 185271530 | |||||
chr1:185271538
|
G | A | 12 | a0003c0005t0003g0003a0003c0005t0003g0228a0003c0005t0003g0246others(9): Show | 13 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.2508+149G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185271538 | ||||||
chr1:185271591
|
A | G | 3 | a0001c0001t0002g0122a0001c0001t0002g0279a0001c0001t0002g0283 | 3 | HG02071.hp2 HG02074.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2508+202A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185271591 | ||||||
chr1:185271611
|
A | G | 5 | a0004c0006t0001g0146a0004c0006t0001g0147a0004c0006t0001g0148others(2): Show | 5 | NA18939.hp2 NA18973.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.2508+222A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185271611 | ||||||
chr1:185272044
|
G | A | 24 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(21): Show | 24 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.2508+655G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272044 | ||||||
chr1:185272055
|
T | A | 3 | a0004c0006t0001g0143a0004c0006t0001g0144a0004c0006t0001g0145 | 3 | HG00738.hp2 HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2508+666T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272055 | ||||||
chr1:185272141
|
G | C | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2508+752G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272141 | ||||||
chr1:185272150
|
G | T | 1 | a0003c0005t0004g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2508+761G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272150 | ||||||
chr1:185272278
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2508+889C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272278 | ||||||
chr1:185272295
|
A | G | 1 | a0011c0020t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2508+906A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272295 | ||||||
chr1:185272301
|
G | C | 1 | a0002c0004t0001g0320 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2508+912G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272301 | ||||||
chr1:185272661
|
A | G | 66 | a0002c0002t0001g0188a0002c0002t0001g0215a0002c0002t0001g0216others(63): Show | 66 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.2508+1272A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185272661 | ||||||
chr1:185273133
|
C | G | 1 | a0003c0005t0004g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2508+1744C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273133 | ||||||
chr1:185273224
|
A | G | 1 | a0002c0004t0001g0318 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2508+1835A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273224 | ||||||
chr1:185273431
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2508+2042G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273431 | ||||||
chr1:185273492
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2508+2103G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273492 | ||||||
chr1:185273571
|
C | G | 1 | a0003c0003t0001g0222 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2508+2182C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273571 | ||||||
chr1:185273606
|
G | A | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2508+2217G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273606 | ||||||
chr1:185273920
|
G | A | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2508+2531G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185273920 | ||||||
chr1:185274221
|
A | G | 1 | a0003c0021t0011g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2509-2383A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274221 | ||||||
chr1:185274233
|
CAT | C | 10 | a0001c0001t0004g0038a0003c0005t0004g0007a0003c0005t0004g0008others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2509-2368_2509-236 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 185274233 | |||||
chr1:185274336
|
G | GAT | 4 | a0001c0001t0001g0006a0008c0012t0001g0019a0008c0012t0001g0020others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2509-2257_2509-225 others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 185274336 | |||||
chr1:185274454
|
G | A | 1 | a0006c0008t0001g0141 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2509-2150G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274454 | ||||||
chr1:185274455
|
C | T | 1 | a0006c0008t0001g0141 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2509-2149C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274455 | ||||||
chr1:185274457
|
G | A | 1 | a0006c0008t0001g0141 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2509-2147G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274457 | ||||||
chr1:185274459
|
T | A | 1 | a0006c0008t0001g0141 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2509-2145T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274459 | ||||||
chr1:185274648
|
A | T | 5 | a0002c0002t0001g0169a0002c0002t0001g0171a0002c0002t0001g0173others(2): Show | 5 | NA18952.hp2 NA18971.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.2509-1956A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274648 | ||||||
chr1:185274721
|
C | G | 1 | a0002c0002t0001g0178 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2509-1883C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274721 | ||||||
chr1:185274749
|
T | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2509-1855T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185274749 | ||||||
chr1:185275184
|
C | T | 1 | a0004c0006t0001g0143 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2509-1420C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275184 | ||||||
chr1:185275436
|
A | C | 155 | a0001c0001t0007g0094a0002c0002t0001g0002a0002c0002t0001g0136others(152): Show | 157 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.2509-1168A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275436 | ||||||
chr1:185275541
|
T | C | 2 | a0003c0005t0003g0252a0003c0005t0003g0255 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2509-1063T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275541 | ||||||
chr1:185275543
|
T | C | 5 | a0003c0005t0003g0003a0003c0005t0003g0246a0003c0005t0003g0247others(2): Show | 6 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2509-1061T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275543 | ||||||
chr1:185275687
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0101 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2509-917A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275687 | ||||||
chr1:185275915
|
G | A | 210 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(207): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2509-689G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185275915 | ||||||
chr1:185276230
|
G | T | 1 | a0002c0002t0001g0219 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2509-374G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185276230 | ||||||
chr1:185276253
|
A | G | 4 | a0007c0010t0001g0071a0007c0010t0001g0072a0007c0010t0001g0073others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-351A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185276253 | ||||||
chr1:185276268
|
G | A | 1 | a0003c0003t0001g0190 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2509-336G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185276268 | ||||||
chr1:185276314
|
T | C | 2 | a0009c0017t0001g0076a0009c0023t0001g0162 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2509-290T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 17/18 | chr1 | 185276314 | ||||||
chr1:185276816
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0119a0001c0011t0001g0161 | 3 | HG01070.hp2 HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2573+148C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185276816 | ||||||
chr1:185277248
|
CTTTA | C | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2573+596_2573+599d others(6): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185277248 | |||||
chr1:185277289
|
T | A | 2 | a0006c0008t0003g0244a0006c0008t0003g0245 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2573+621T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277289 | ||||||
chr1:185277352
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2573+684G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277352 | ||||||
chr1:185277361
|
T | A | 1 | a0001c0001t0001g0111 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2573+693T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277361 | ||||||
chr1:185277558
|
G | A | 1 | a0002c0002t0001g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2573+890G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277558 | ||||||
chr1:185277612
|
A | G | 6 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(3): Show | 6 | NA18964.hp2 NA18972.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.2573+944A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277612 | ||||||
chr1:185277628
|
T | A | 1 | a0002c0002t0001g0217 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2573+960T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277628 | ||||||
chr1:185277672
|
C | T | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2573+1004C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277672 | ||||||
chr1:185277836
|
G | C | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2573+1168G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185277836 | ||||||
chr1:185278024
|
A | G | 15 | a0003c0003t0001g0235a0003c0003t0001g0236a0003c0003t0001g0237others(12): Show | 15 | HG01099.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2573+1356A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278024 | ||||||
chr1:185278050
|
C | T | 2 | a0003c0003t0001g0263a0003c0003t0001g0264 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2573+1382C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278050 | ||||||
chr1:185278119
|
T | C | 210 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(207): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2573+1451T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278119 | ||||||
chr1:185278120
|
G | A | 1 | a0002c0002t0001g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2573+1452G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278120 | ||||||
chr1:185278137
|
A | G | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2573+1469A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278137 | ||||||
chr1:185278336
|
G | C | 210 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(207): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2573+1668G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278336 | ||||||
chr1:185278421
|
A | T | 210 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(207): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2573+1753A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278421 | ||||||
chr1:185278662
|
G | A | 214 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0012others(211): Show | 216 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.2573+1994G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278662 | ||||||
chr1:185278927
|
G | A | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2573+2259G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278927 | ||||||
chr1:185278969
|
G | A | 1 | a0003c0003t0001g0263 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2573+2301G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185278969 | ||||||
chr1:185279061
|
G | A | 3 | a0008c0012t0001g0019a0008c0012t0001g0020a0008c0012t0001g0021 | 3 | HG02145.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2573+2393G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279061 | ||||||
chr1:185279132
|
A | G | 1 | a0002c0002t0001g0218 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2573+2464A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279132 | ||||||
chr1:185279139
|
C | T | 1 | a0003c0005t0001g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2573+2471C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279139 | ||||||
chr1:185279140
|
G | T | 2 | a0001c0001t0001g0129a0012c0018t0001g0029 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2573+2472G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279140 | ||||||
chr1:185279301
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2573+2633C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279301 | ||||||
chr1:185279302
|
G | A | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2573+2634G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279302 | ||||||
chr1:185279378
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2573+2710G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279378 | ||||||
chr1:185279744
|
G | A | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2573+3076G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279744 | ||||||
chr1:185279918
|
A | T | 1 | a0002c0004t0001g0308 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2573+3250A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279918 | ||||||
chr1:185279926
|
A | G | 1 | a0003c0003t0001g0211 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2573+3258A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185279926 | ||||||
chr1:185280082
|
G | C | 210 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(207): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.2573+3414G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280082 | ||||||
chr1:185280115
|
T | C | 1 | a0001c0011t0008g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2573+3447T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280115 | ||||||
chr1:185280574
|
G | A | 1 | a0003c0021t0011g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2573+3906G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280574 | ||||||
chr1:185280672
|
A | G | 35 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.2573+4004A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280672 | ||||||
chr1:185280699
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2573+4031C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280699 | ||||||
chr1:185280868
|
G | A | 1 | a0016c0024t0001g0176 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2573+4200G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280868 | ||||||
chr1:185280950
|
G | A | 3 | a0004c0006t0001g0164a0004c0006t0001g0165a0004c0009t0001g0068 | 3 | HG01070.hp1 HG01081.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2573+4282G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185280950 | ||||||
chr1:185281222
|
T | G | 3 | a0001c0001t0007g0094a0003c0005t0009g0004a0003c0021t0011g0132 | 3 | HG02109.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2573+4554T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185281222 | ||||||
chr1:185281489
|
G | A | 1 | a0002c0004t0001g0312 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2573+4821G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185281489 | ||||||
chr1:185281499
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2573+4831C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185281499 | ||||||
chr1:185281894
|
C | G | 1 | a0002c0004t0001g0309 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2573+5226C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185281894 | ||||||
chr1:185282376
|
TA | T | 15 | a0002c0002t0001g0138a0002c0002t0001g0154a0003c0005t0003g0003others(12): Show | 16 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.2573+5720delA | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185282376 | |||||
chr1:185282596
|
T | C | 10 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0171others(7): Show | 10 | HG02132.hp2 NA18944.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.2573+5928T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185282596 | ||||||
chr1:185282793
|
C | T | 3 | a0001c0001t0001g0095a0003c0005t0001g0231a0003c0005t0001g0232 | 3 | HG00735.hp1 HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2573+6125C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185282793 | ||||||
chr1:185282819
|
A | T | 1 | a0003c0005t0003g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2573+6151A>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185282819 | ||||||
chr1:185282853
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2573+6185G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185282853 | ||||||
chr1:185283321
|
C | G | 5 | a0002c0002t0001g0169a0002c0002t0001g0171a0002c0002t0001g0173others(2): Show | 5 | NA18952.hp2 NA18971.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.2573+6653C>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185283321 | ||||||
chr1:185283341
|
G | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0067 | 2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2573+6673G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185283341 | ||||||
chr1:185283426
|
A | G | 14 | a0002c0002t0001g0002a0002c0002t0001g0151a0002c0002t0001g0170others(11): Show | 15 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.2573+6758A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185283426 | ||||||
chr1:185283481
|
A | C | 1 | a0001c0001t0001g0127 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2573+6813A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185283481 | ||||||
chr1:185283550
|
T | TTTTG | 37 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(34): Show | 37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2573+6901_2573+690 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185283550 | |||||
chr1:185283550
|
TTTTG | T | 11 | a0002c0002t0001g0002a0002c0002t0001g0151a0002c0002t0001g0170others(8): Show | 12 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.2573+6901_2573+690 others(8): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185283550 | |||||
chr1:185283873
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2574-6801T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185283873 | ||||||
chr1:185284168
|
C | T | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2574-6506C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284168 | ||||||
chr1:185284456
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2574-6218C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284456 | ||||||
chr1:185284478
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2574-6196C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284478 | ||||||
chr1:185284658
|
T | G | 217 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0066others(214): Show | 219 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.2574-6016T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284658 | ||||||
chr1:185284689
|
T | G | 37 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(34): Show | 37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2574-5985T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284689 | ||||||
chr1:185284734
|
G | A | 37 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(34): Show | 37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2574-5940G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284734 | ||||||
chr1:185284782
|
C | T | 5 | a0007c0010t0001g0071a0007c0010t0001g0072a0007c0010t0001g0073others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2574-5892C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284782 | ||||||
chr1:185284876
|
C | T | 6 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2574-5798C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284876 | ||||||
chr1:185284884
|
A | C | 2 | a0003c0003t0001g0263a0003c0003t0001g0264 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2574-5790A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284884 | ||||||
chr1:185284889
|
C | CT | 6 | a0001c0001t0001g0040a0001c0001t0001g0091a0001c0001t0001g0105others(3): Show | 6 | HG00140.hp1 HG00741.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2574-5771dupT | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185284889 | |||||
chr1:185284992
|
G | C | 1 | a0013c0016t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2574-5682G>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185284992 | ||||||
chr1:185285684
|
T | C | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2574-4990T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185285684 | ||||||
chr1:185285879
|
T | A | 2 | a0003c0003t0001g0208a0003c0003t0001g0222 | 2 | HG02080.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2574-4795T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185285879 | ||||||
chr1:185285893
|
T | C | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2574-4781T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185285893 | ||||||
chr1:185286286
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0118a0004c0006t0001g0226 | 3 | HG00408.hp1 HG02630.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2574-4388C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286286 | ||||||
chr1:185286487
|
G | A | 3 | a0002c0002t0001g0138a0002c0002t0001g0154a0015c0022t0001g0009 | 3 | HG01884.hp2 HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2574-4187G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286487 | ||||||
chr1:185286563
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0067 | 2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2574-4111C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286563 | ||||||
chr1:185286585
|
G | T | 3 | a0003c0005t0004g0007a0003c0005t0004g0008a0003c0005t0004g0230 | 3 | HG01891.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2574-4089G>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286585 | ||||||
chr1:185286653
|
T | A | 1 | a0001c0001t0002g0274 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2574-4021T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286653 | ||||||
chr1:185286734
|
A | C | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | NA18973.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2574-3940A>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286734 | ||||||
chr1:185286831
|
T | C | 1 | a0001c0001t0007g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2574-3843T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286831 | ||||||
chr1:185286936
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2574-3738T>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286936 | ||||||
chr1:185286960
|
T | C | 2 | a0002c0004t0001g0300a0002c0004t0001g0301 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2574-3714T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185286960 | ||||||
chr1:185287358
|
G | A | 12 | a0001c0001t0004g0038a0003c0003t0004g0233a0003c0003t0004g0234others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2574-3316G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185287358 | ||||||
chr1:185287576
|
G | A | 25 | a0003c0003t0001g0190a0003c0003t0001g0191a0003c0003t0001g0192others(22): Show | 25 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.2574-3098G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185287576 | ||||||
chr1:185287617
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2574-3057T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185287617 | ||||||
chr1:185287929
|
T | C | 212 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0002g0011others(209): Show | 214 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.2574-2745T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185287929 | ||||||
chr1:185287930
|
T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG00438.hp1 HG02071.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2574-2744T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185287930 | ||||||
chr1:185288067
|
C | T | 6 | a0003c0003t0001g0271a0003c0003t0001g0272a0006c0008t0001g0139others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2574-2607C>T | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288067 | ||||||
chr1:185288080
|
G | A | 1 | a0003c0003t0001g0208 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2574-2594G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288080 | ||||||
chr1:185288137
|
T | A | 1 | a0002c0004t0001g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2574-2537T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288137 | ||||||
chr1:185288440
|
A | G | 1 | a0005c0007t0001g0243 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2574-2234A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288440 | ||||||
chr1:185288584
|
T | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0063a0001c0001t0001g0065others(3): Show | 6 | HG00621.hp1 NA18970.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2574-2090T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288584 | ||||||
chr1:185288736
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0067 | 2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2574-1938A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288736 | ||||||
chr1:185288773
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0127 | 2 | NA18943.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.2574-1901G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185288773 | ||||||
chr1:185289395
|
T | C | 38 | a0001c0001t0004g0038a0003c0003t0001g0190a0003c0003t0001g0191others(35): Show | 38 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.2574-1279T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185289395 | ||||||
chr1:185289509
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0067 | 2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2574-1165A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185289509 | ||||||
chr1:185289560
|
A | G | 1 | a0004c0006t0001g0223 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2574-1114A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185289560 | ||||||
chr1:185289731
|
CATT | C | 14 | a0003c0005t0003g0003a0003c0005t0003g0228a0003c0005t0003g0246others(11): Show | 15 | HG02055.hp2 HG02451.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2574-941_2574-939d others(5): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185289731 | |||||
chr1:185289801
|
T | C | 2 | a0001c0001t0001g0069a0001c0011t0001g0161 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2574-873T>C | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185289801 | ||||||
chr1:185290111
|
GCAAAACA others(3): Show |
G | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2574-552_2574-543d others(12): Show |
SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 185290111 | |||||
chr1:185290293
|
A | G | 2 | a0003c0005t0001g0231a0003c0005t0001g0232 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2574-381A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185290293 | ||||||
chr1:185290299
|
G | A | 1 | a0002c0002t0001g0154 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2574-375G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185290299 | ||||||
chr1:185290500
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2574-174G>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185290500 | ||||||
chr1:185290576
|
T | A | 8 | a0003c0003t0001g0155a0003c0003t0001g0156a0003c0003t0001g0212others(5): Show | 8 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2574-98T>A | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185290576 | ||||||
chr1:185290599
|
A | G | 129 | a0001c0001t0001g0064a0001c0001t0005g0100a0002c0002t0001g0002others(126): Show | 130 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.2574-75A>G | SWT1 | ENSG00000116668.13 | transcript | ENST00000367500.9 | protein_coding | 18/18 | chr1 | 185290599 |