geneid | 23013 |
---|---|
ensemblid | ENSG00000065526.13 |
hgncid | 17575 |
symbol | SPEN |
name | spen family transcriptional repressor |
refseq_nuc | NM_015001.3 |
refseq_prot | NP_055816.2 |
ensembl_nuc | ENST00000375759.8 |
ensembl_prot | ENSP00000364912.3 |
mane_status | MANE Select |
chr | chr1 |
start | 15847707 |
end | 15940456 |
strand | + |
ver | v1.2 |
region | chr1:15847707-15940456 |
region5000 | chr1:15842707-15945456 |
regionname0 | SPEN_chr1_15847707_15940456 |
regionname5000 | SPEN_chr1_15842707_15945456 |
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 | 0/1 | 3664 | 118 | 51 | 27 | 10 | 11 | 18 | 5 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0002 | 1/0 | 3664 | 73 | 2 | 13 | 46 | 1 | 10 | 35 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0003 | 0/0 | 3664 | 65 | 3 | 12 | 46 | 0 | 4 | 33 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0004 | 0/0 | 3664 | 10 | 7 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0005 | 0/0 | 3664 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0006 | 0/0 | 3664 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0007 | 0/0 | 3664 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0008 | 0/0 | 3664 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0009 | 0/0 | 3663 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0010 | 0/0 | 3664 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0011 | 0/0 | 3664 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0012 | 0/0 | 3664 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0013 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0014 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0015 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0016 | 0/0 | 3664 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0017 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0018 | 0/0 | 3664 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0019 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0020 | 0/0 | 3664 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0021 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0022 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0023 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0024 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0025 | 0/0 | 3664 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
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 | 0/1 | 10995 | 89 | 35 | 22 | 5 | 9 | 17 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0002 | 1/0 | 10995 | 72 | 2 | 13 | 45 | 1 | 10 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0003 | 0/0 | 10995 | 65 | 3 | 12 | 46 | 0 | 4 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0004 | 0/0 | 10995 | 12 | 6 | 2 | 3 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0005 | 0/0 | 10995 | 8 | 6 | 2 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0006 | 0/0 | 10995 | 7 | 4 | 3 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0007 | 0/0 | 10995 | 4 | 4 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0008 | 0/0 | 10995 | 3 | 2 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0009 | 0/0 | 10995 | 3 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0010 | 0/0 | 10995 | 3 | 0 | 0 | 3 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0011 | 0/0 | 10992 | 3 | 0 | 2 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0012 | 0/0 | 10995 | 3 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0013 | 0/0 | 10995 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0014 | 0/0 | 10995 | 2 | 0 | 1 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0015 | 0/0 | 10995 | 2 | 0 | 0 | 2 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0016 | 0/0 | 10995 | 2 | 0 | 0 | 0 | 0 | 2 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0017 | 0/0 | 10995 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0018 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0019 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0020 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0021 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0022 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0023 | 0/0 | 10995 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0024 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0025 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0026 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0027 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0028 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0029 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0030 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0031 | 0/0 | 10995 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0032 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0033 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0034 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0035 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0036 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0037 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0038 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
c0039 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
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 | 1391 | 297 | 77 | 63 | 109 | 13 | 33 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
t0002 | 0/0 | 1391 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
t0003 | 0/0 | 1391 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
t0004 | 0/0 | 1391 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
t0005 | 0/0 | 1391 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
t0006 | 0/0 | 1391 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
t0007 | 0/0 | 1391 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
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 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0013 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
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 | 0/1 | 10995 | 89 | 35 | 22 | 5 | 9 | 17 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0004 | 0/0 | 10995 | 12 | 6 | 2 | 3 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0007 | 0/0 | 10995 | 4 | 4 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0014 | 0/0 | 10995 | 2 | 0 | 1 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0015 | 0/0 | 10995 | 2 | 0 | 0 | 2 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0017 | 0/0 | 10995 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0023 | 0/0 | 10995 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0026 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0027 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0028 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0029 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0037 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0038 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0002c0002 | 1/0 | 10995 | 72 | 2 | 13 | 45 | 1 | 10 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0002c0018 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0003c0003 | 0/0 | 10995 | 65 | 3 | 12 | 46 | 0 | 4 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0004c0006 | 0/0 | 10995 | 7 | 4 | 3 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0004c0009 | 0/0 | 10995 | 3 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0005c0005 | 0/0 | 10995 | 8 | 6 | 2 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0006c0012 | 0/0 | 10995 | 3 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0007c0010 | 0/0 | 10995 | 3 | 0 | 0 | 3 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0008c0008 | 0/0 | 10995 | 3 | 2 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0009c0011 | 0/0 | 10992 | 3 | 0 | 2 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0010c0016 | 0/0 | 10995 | 2 | 0 | 0 | 0 | 0 | 2 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0011c0013 | 0/0 | 10995 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0012c0019 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0013c0033 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0014c0034 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0015c0021 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0016c0022 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0017c0024 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0018c0025 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0019c0030 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0020c0031 | 0/0 | 10995 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0021c0032 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0022c0020 | 0/0 | 10995 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0023c0035 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0024c0036 | 0/0 | 10995 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0025c0039 | 0/0 | 10995 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 12385 | 87 | 34 | 21 | 5 | 9 | 17 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0001t0005 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0001t0006 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0004t0001 | 0/0 | 12385 | 12 | 6 | 2 | 3 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0007t0001 | 0/0 | 12385 | 4 | 4 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0014t0001 | 0/0 | 12385 | 2 | 0 | 1 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0015t0001 | 0/0 | 12385 | 2 | 0 | 0 | 2 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0017t0001 | 0/0 | 12385 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0023t0003 | 0/0 | 12385 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0026t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0027t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0028t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0029t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0037t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0001c0038t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0002c0002t0001 | 1/0 | 12385 | 71 | 2 | 13 | 44 | 1 | 10 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0002c0002t0004 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0002c0018t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0003c0003t0001 | 0/0 | 12385 | 64 | 3 | 12 | 46 | 0 | 3 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0003c0003t0007 | 0/0 | 12385 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0004c0006t0001 | 0/0 | 12385 | 7 | 4 | 3 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0004c0009t0001 | 0/0 | 12385 | 3 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0005c0005t0001 | 0/0 | 12385 | 8 | 6 | 2 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0006c0012t0001 | 0/0 | 12385 | 3 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0007c0010t0001 | 0/0 | 12385 | 3 | 0 | 0 | 3 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0008c0008t0001 | 0/0 | 12385 | 3 | 2 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0009c0011t0001 | 0/0 | 12382 | 3 | 0 | 2 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0010c0016t0001 | 0/0 | 12385 | 2 | 0 | 0 | 0 | 0 | 2 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0011c0013t0002 | 0/0 | 12385 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0012c0019t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0013c0033t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0014c0034t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0015c0021t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0016c0022t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0017c0024t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0018c0025t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0019c0030t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0020c0031t0001 | 0/0 | 12385 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0021c0032t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0022c0020t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0023c0035t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0024c0036t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
a0025c0039t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | copy fasta | chr1 | 15842707 | 15945456 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0013 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0007t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0007t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0007t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0007t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0014t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0014t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0015t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0015t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0017t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0017t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0023t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0026t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0027t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0028t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0029t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0037t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0038t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0018t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0007g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0009t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0009t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0009t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0005t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0005t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0005t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0005t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0005t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0006c0012t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0006c0012t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0006c0012t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0007c0010t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0007c0010t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0007c0010t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0008c0008t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0008c0008t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0008c0008t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0009c0011t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0009c0011t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0009c0011t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0010c0016t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0010c0016t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0011c0013t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0011c0013t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0012c0019t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0013c0033t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0014c0034t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0015c0021t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0016c0022t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0017c0024t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0018c0025t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0019c0030t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0020c0031t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0021c0032t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0022c0020t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0023c0035t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0024c0036t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0025c0039t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00280 | hp2 | a0009 | c0011 | t0001 | g0159 | EUR | FIN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0227 | EUR | FIN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00323 | hp2 | a0001 | c0014 | t0001 | g0019 | EUR | FIN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00423 | hp1 | a0003 | c0003 | t0001 | g0183 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00423 | hp2 | a0003 | c0003 | t0001 | g0167 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00438 | hp1 | a0003 | c0003 | t0001 | g0138 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0137 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00558 | hp1 | a0003 | c0003 | t0001 | g0109 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00558 | hp2 | a0014 | c0034 | t0001 | g0265 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00642 | hp1 | a0018 | c0025 | t0001 | g0043 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00673 | hp2 | a0003 | c0003 | t0001 | g0187 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00735 | hp1 | a0001 | c0026 | t0001 | g0096 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00741 | hp2 | a0001 | c0038 | t0001 | g0093 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01069 | hp1 | a0001 | c0014 | t0001 | g0034 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01069 | hp2 | a0005 | c0005 | t0001 | g0208 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01070 | hp1 | a0004 | c0006 | t0001 | g0112 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0286 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01071 | hp1 | a0005 | c0005 | t0001 | g0209 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01071 | hp2 | a0004 | c0006 | t0001 | g0113 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01074 | hp2 | a0001 | c0004 | t0001 | g0083 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01099 | hp2 | a0001 | c0004 | t0001 | g0095 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01109 | hp2 | a0004 | c0006 | t0001 | g0117 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01167 | hp1 | a0008 | c0008 | t0001 | g0099 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0172 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01192 | hp1 | a0012 | c0019 | t0001 | g0035 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01192 | hp2 | a0025 | c0039 | t0001 | g0125 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0097 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0279 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01255 | hp2 | a0003 | c0003 | t0001 | g0173 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01256 | hp2 | a0003 | c0003 | t0001 | g0123 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0271 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0229 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01346 | hp2 | a0003 | c0003 | t0001 | g0170 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01361 | hp2 | a0003 | c0003 | t0001 | g0130 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01433 | hp1 | a0003 | c0003 | t0001 | g0128 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0264 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01496 | hp1 | a0009 | c0011 | t0001 | g0003 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01515 | hp2 | a0001 | c0023 | t0003 | g0006 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01516 | hp1 | a0020 | c0031 | t0001 | g0007 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01891 | hp2 | a0005 | c0005 | t0001 | g0210 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01928 | hp1 | a0003 | c0003 | t0001 | g0146 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01934 | hp2 | a0009 | c0011 | t0001 | g0175 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01943 | hp1 | a0003 | c0003 | t0001 | g0127 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01975 | hp1 | a0003 | c0003 | t0001 | g0129 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01975 | hp2 | a0016 | c0022 | t0001 | g0012 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02015 | hp1 | a0003 | c0003 | t0001 | g0145 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02040 | hp1 | a0003 | c0003 | t0001 | g0144 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0166 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02083 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02132 | hp1 | a0001 | c0015 | t0001 | g0046 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02132 | hp2 | a0003 | c0003 | t0001 | g0136 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02145 | hp1 | a0019 | c0030 | t0001 | g0080 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | CDX | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02257 | hp2 | a0005 | c0005 | t0001 | g0212 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02273 | hp1 | a0003 | c0003 | t0001 | g0126 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0168 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02293 | hp2 | a0003 | c0003 | t0001 | g0132 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02572 | hp1 | a0022 | c0020 | t0001 | g0110 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0089 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0270 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02602 | hp2 | a0003 | c0003 | t0007 | g0162 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02615 | hp2 | a0001 | c0027 | t0001 | g0076 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02622 | hp1 | a0005 | c0005 | t0001 | g0204 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02630 | hp1 | a0005 | c0005 | t0001 | g0288 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02630 | hp2 | a0003 | c0003 | t0001 | g0169 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02647 | hp2 | a0004 | c0006 | t0001 | g0116 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0178 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0248 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02738 | hp1 | a0003 | c0003 | t0001 | g0141 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02809 | hp1 | a0006 | c0012 | t0001 | g0105 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02818 | hp2 | a0008 | c0008 | t0001 | g0100 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02886 | hp1 | a0011 | c0013 | t0002 | g0054 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02895 | hp2 | a0004 | c0009 | t0001 | g0118 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02896 | hp1 | a0006 | c0012 | t0001 | g0104 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02896 | hp2 | a0001 | c0037 | t0001 | g0197 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02897 | hp1 | a0006 | c0012 | t0001 | g0103 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02922 | hp2 | a0008 | c0008 | t0001 | g0101 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02970 | hp1 | a0004 | c0009 | t0001 | g0114 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02976 | hp2 | a0004 | c0006 | t0001 | g0115 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0177 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0241 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03130 | hp1 | a0001 | c0007 | t0001 | g0294 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03139 | hp1 | a0017 | c0024 | t0001 | g0304 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03225 | hp1 | a0001 | c0017 | t0001 | g0049 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03225 | hp2 | a0001 | c0028 | t0001 | g0088 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03453 | hp2 | a0004 | c0009 | t0001 | g0189 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03486 | hp1 | a0011 | c0013 | t0002 | g0055 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0242 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0246 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03516 | hp1 | a0001 | c0017 | t0001 | g0060 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0092 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03579 | hp1 | a0005 | c0005 | t0001 | g0211 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03579 | hp2 | a0001 | c0007 | t0001 | g0295 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0228 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0231 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04115 | hp2 | a0010 | c0016 | t0001 | g0222 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04184 | hp2 | a0010 | c0016 | t0001 | g0284 | SAS | BEB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0233 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04204 | hp2 | a0001 | c0004 | t0001 | g0084 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0256 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | YRI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | CHB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18612 | hp2 | a0003 | c0003 | t0001 | g0303 | EAS | CHB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | CHB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18747 | hp2 | a0003 | c0003 | t0001 | g0140 | EAS | CHB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18941 | hp1 | a0003 | c0003 | t0001 | g0142 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18943 | hp1 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18944 | hp1 | a0003 | c0003 | t0001 | g0139 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18950 | hp1 | a0003 | c0003 | t0001 | g0163 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18952 | hp2 | a0001 | c0004 | t0001 | g0081 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0135 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18954 | hp1 | a0013 | c0033 | t0001 | g0217 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18957 | hp1 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18961 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18965 | hp2 | a0001 | c0004 | t0001 | g0275 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18966 | hp1 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18968 | hp1 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18971 | hp1 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18973 | hp2 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18977 | hp2 | a0023 | c0035 | t0001 | g0176 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18978 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18980 | hp1 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18984 | hp1 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18987 | hp1 | a0003 | c0003 | t0001 | g0122 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18987 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18995 | hp2 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18998 | hp1 | a0003 | c0003 | t0001 | g0124 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19003 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19004 | hp1 | a0003 | c0003 | t0001 | g0186 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19005 | hp2 | a0021 | c0032 | t0001 | g0087 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19007 | hp1 | a0002 | c0002 | t0004 | g0244 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0150 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19010 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19011 | hp1 | a0024 | c0036 | t0001 | g0164 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19011 | hp2 | a0002 | c0018 | t0001 | g0276 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19030 | hp1 | a0005 | c0005 | t0001 | g0287 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19043 | hp1 | a0001 | c0004 | t0001 | g0085 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19043 | hp2 | a0003 | c0003 | t0001 | g0133 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19054 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19064 | hp1 | a0007 | c0010 | t0001 | g0220 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19064 | hp2 | a0003 | c0003 | t0001 | g0184 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19066 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19067 | hp1 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19068 | hp1 | a0007 | c0010 | t0001 | g0218 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19068 | hp2 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19074 | hp1 | a0003 | c0003 | t0001 | g0171 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19079 | hp1 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19079 | hp2 | a0007 | c0010 | t0001 | g0219 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19087 | hp2 | a0003 | c0003 | t0001 | g0188 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19090 | hp1 | a0001 | c0015 | t0001 | g0062 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19090 | hp2 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19240 | hp1 | a0001 | c0004 | t0001 | g0090 | AFR | YRI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19240 | hp2 | a0001 | c0007 | t0001 | g0293 | AFR | YRI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0282 | AFR | ASW | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20129 | hp2 | a0004 | c0006 | t0001 | g0111 | AFR | ASW | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | GIH | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | GIH | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0131 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02486 | hp1 | a0001 | c0004 | t0001 | g0091 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02486 | hp2 | a0004 | c0006 | t0001 | g0002 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02559 | hp1 | a0001 | c0029 | t0001 | g0094 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG06807 | hp2 | a0001 | c0007 | t0001 | g0296 | AFR | USA | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20300 | hp1 | a0001 | c0004 | t0001 | g0064 | AFR | USA | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | USA | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA21309 | hp2 | a0015 | c0021 | t0001 | g0063 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0013 | REF | REF | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0107 | REF | REF | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15876500
|
C | T | 1 | a0025 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.703C>T | p.Arg235Trp | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/15 | 1064/12385 | 703/10995 | 235/3664 | chr1 | 15876500 | ||
chr1:15920891
|
G | A | 1 | a0011 | 2 | HG02886.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.1657G>A | p.Gly553Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/15 | 2018/12385 | 1657/10995 | 553/3664 | chr1 | 15920891 | ||
chr1:15928591
|
G | A | 1 | a0012 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.2351G>A | p.Arg784His | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 2712/12385 | 2351/10995 | 784/3664 | chr1 | 15928591 | ||
chr1:15928710
|
C | T | 1 | a0006 | 3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.2470C>T | p.Arg824Cys | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 2831/12385 | 2470/10995 | 824/3664 | chr1 | 15928710 | ||
chr1:15929149
|
C | T | 5 | a0003a0009a0023others(2): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
missense_variant | MODERATE | c.2909C>T | p.Ala970Val | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 3270/12385 | 2909/10995 | 970/3664 | chr1 | 15929149 | ||
chr1:15929259
|
C | A | 1 | a0022 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.3019C>A | p.Pro1007Thr | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 3380/12385 | 3019/10995 | 1007/3664 | chr1 | 15929259 | ||
chr1:15929304
|
G | A | 1 | a0012 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.3064G>A | p.Val1022Met | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 3425/12385 | 3064/10995 | 1022/3664 | chr1 | 15929304 | ||
chr1:15929511
|
C | G | 1 | a0005 | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
missense_variant | MODERATE | c.3271C>G | p.Leu1091Val | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 3632/12385 | 3271/10995 | 1091/3664 | chr1 | 15929511 | ||
chr1:15929512
|
T | C | 20 | a0001a0003a0004others(17): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
missense_variant | MODERATE | c.3272T>C | p.Leu1091Pro | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 3633/12385 | 3272/10995 | 1091/3664 | chr1 | 15929512 | ||
chr1:15931150
|
T | C | 2 | a0008a0015 | 4 | HG01167.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
missense_variant | MODERATE | c.4910T>C | p.Val1637Ala | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 5271/12385 | 4910/10995 | 1637/3664 | chr1 | 15931150 | ||
chr1:15931311
|
C | T | 1 | a0024 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.5071C>T | p.Pro1691Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 5432/12385 | 5071/10995 | 1691/3664 | chr1 | 15931311 | ||
chr1:15931623
|
C | T | 1 | a0021 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.5383C>T | p.Pro1795Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 5744/12385 | 5383/10995 | 1795/3664 | chr1 | 15931623 | ||
chr1:15931807
|
A | G | 1 | a0020 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.5567A>G | p.Asn1856Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 5928/12385 | 5567/10995 | 1856/3664 | chr1 | 15931807 | ||
chr1:15932188
|
C | T | 1 | a0022 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.5948C>T | p.Ser1983Leu | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6309/12385 | 5948/10995 | 1983/3664 | chr1 | 15932188 | ||
chr1:15932307
|
G | A | 1 | a0016 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.6067G>A | p.Val2023Met | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6428/12385 | 6067/10995 | 2023/3664 | chr1 | 15932307 | ||
chr1:15932413
|
C | T | 1 | a0014 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.6173C>T | p.Ala2058Val | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6534/12385 | 6173/10995 | 2058/3664 | chr1 | 15932413 | ||
chr1:15932440
|
C | T | 1 | a0010 | 2 | HG04115.hp2 HG04184.hp2 |
missense_variant | MODERATE | c.6200C>T | p.Pro2067Leu | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6561/12385 | 6200/10995 | 2067/3664 | chr1 | 15932440 | ||
chr1:15932835
|
G | T | 1 | a0023 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.6595G>T | p.Ala2199Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6956/12385 | 6595/10995 | 2199/3664 | chr1 | 15932835 | ||
chr1:15932959
|
C | T | 2 | a0007a0013 | 4 | NA18954.hp1 NA19064.hp1 NA19068.hp1 others(1): Show |
missense_variant | MODERATE | c.6719C>T | p.Pro2240Leu | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7080/12385 | 6719/10995 | 2240/3664 | chr1 | 15932959 | ||
chr1:15933152
|
TAGC | T | 1 | a0009 | 3 | HG00280.hp2 HG01496.hp1 HG01934.hp2 |
disruptive_inframe_deletion | MODERATE | c.6915_6917delCAG | p.Ser2306del | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7276/12385 | 6915/10995 | 2305/3664 | INFO_REALIGN_3_PRIME | chr1 | 15933152 | |
chr1:15933318
|
A | G | 20 | a0001a0003a0004others(17): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
missense_variant | MODERATE | c.7078A>G | p.Asn2360Asp | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7439/12385 | 7078/10995 | 2360/3664 | chr1 | 15933318 | ||
chr1:15933420
|
C | T | 1 | a0019 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.7180C>T | p.Pro2394Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7541/12385 | 7180/10995 | 2394/3664 | chr1 | 15933420 | ||
chr1:15933897
|
A | G | 1 | a0008 | 3 | HG01167.hp1 HG02818.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.7657A>G | p.Ser2553Gly | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8018/12385 | 7657/10995 | 2553/3664 | chr1 | 15933897 | ||
chr1:15934018
|
A | G | 2 | a0004a0022 | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
missense_variant | MODERATE | c.7778A>G | p.Asn2593Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8139/12385 | 7778/10995 | 2593/3664 | chr1 | 15934018 | ||
chr1:15934308
|
G | A | 1 | a0017 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.8068G>A | p.Val2690Met | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8429/12385 | 8068/10995 | 2690/3664 | chr1 | 15934308 | ||
chr1:15934428
|
A | T | 1 | a0013 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.8188A>T | p.Ser2730Cys | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8549/12385 | 8188/10995 | 2730/3664 | chr1 | 15934428 | ||
chr1:15937527
|
G | C | 1 | a0018 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.10391G>C | p.Gly3464Ala | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 12/15 | 10752/12385 | 10391/10995 | 3464/3664 | chr1 | 15937527 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15872927
|
G | A | 1 | a0002c0018 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.195G>A | p.Ser65Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/15 | 556/12385 | 195/10995 | 65/3664 | chr1 | 15872927 | ||
chr1:15919484
|
A | T | 1 | a0001c0017 | 2 | HG03225.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.1602A>T | p.Thr534Thr | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/15 | 1963/12385 | 1602/10995 | 534/3664 | chr1 | 15919484 | ||
chr1:15919487
|
A | C | 1 | a0001c0038 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.1605A>C | p.Arg535Arg | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/15 | 1966/12385 | 1605/10995 | 535/3664 | chr1 | 15919487 | ||
chr1:15928412
|
A | G | 1 | a0001c0037 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.2172A>G | p.Arg724Arg | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 2533/12385 | 2172/10995 | 724/3664 | chr1 | 15928412 | ||
chr1:15930761
|
A | G | 3 | a0004c0006a0004c0009a0022c0020 | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
synonymous_variant | LOW | c.4521A>G | p.Lys1507Lys | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 4882/12385 | 4521/10995 | 1507/3664 | chr1 | 15930761 | ||
chr1:15932066
|
A | T | 1 | a0001c0015 | 2 | HG02132.hp1 NA19090.hp1 |
synonymous_variant | LOW | c.5826A>T | p.Ala1942Ala | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6187/12385 | 5826/10995 | 1942/3664 | chr1 | 15932066 | ||
chr1:15932648
|
G | A | 5 | a0001c0007a0001c0023a0004c0006others(2): Show | 16 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(13): Show |
synonymous_variant | LOW | c.6408G>A | p.Gln2136Gln | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6769/12385 | 6408/10995 | 2136/3664 | chr1 | 15932648 | ||
chr1:15933164
|
C | T | 2 | a0001c0029a0019c0030 | 2 | HG02145.hp1 HG02559.hp1 |
synonymous_variant | LOW | c.6924C>T | p.Thr2308Thr | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7285/12385 | 6924/10995 | 2308/3664 | chr1 | 15933164 | ||
chr1:15933374
|
C | T | 1 | a0001c0028 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.7134C>T | p.Pro2378Pro | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7495/12385 | 7134/10995 | 2378/3664 | chr1 | 15933374 | ||
chr1:15933887
|
C | T | 1 | a0001c0027 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.7647C>T | p.Val2549Val | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8008/12385 | 7647/10995 | 2549/3664 | chr1 | 15933887 | ||
chr1:15934421
|
C | T | 5 | a0003c0003a0009c0011a0023c0035others(2): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
synonymous_variant | LOW | c.8181C>T | p.Ala2727Ala | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8542/12385 | 8181/10995 | 2727/3664 | chr1 | 15934421 | ||
chr1:15934460
|
C | G | 1 | a0001c0026 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.8220C>G | p.Thr2740Thr | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8581/12385 | 8220/10995 | 2740/3664 | chr1 | 15934460 | ||
chr1:15935319
|
C | A | 1 | a0001c0014 | 2 | HG00323.hp2 HG01069.hp1 |
synonymous_variant | LOW | c.9079C>A | p.Arg3027Arg | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 9440/12385 | 9079/10995 | 3027/3664 | chr1 | 15935319 | ||
chr1:15935861
|
C | T | 1 | a0004c0006 | 7 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(4): Show |
synonymous_variant | LOW | c.9621C>T | p.Ser3207Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 9982/12385 | 9621/10995 | 3207/3664 | chr1 | 15935861 | ||
chr1:15935909
|
C | T | 5 | a0003c0003a0009c0011a0023c0035others(2): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
synonymous_variant | LOW | c.9669C>T | p.Ser3223Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 10030/12385 | 9669/10995 | 3223/3664 | chr1 | 15935909 | ||
chr1:15936224
|
T | C | 3 | a0004c0006a0004c0009a0022c0020 | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
synonymous_variant | LOW | c.9984T>C | p.Ala3328Ala | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 10345/12385 | 9984/10995 | 3328/3664 | chr1 | 15936224 | ||
chr1:15937621
|
C | T | 1 | a0001c0007 | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.10485C>T | p.Pro3495Pro | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 12/15 | 10846/12385 | 10485/10995 | 3495/3664 | chr1 | 15937621 | ||
chr1:15937835
|
C | T | 1 | a0001c0038 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.10533C>T | p.Gly3511Gly | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/15 | 10894/12385 | 10533/10995 | 3511/3664 | chr1 | 15937835 | ||
chr1:15939409
|
T | A | 4 | a0001c0004a0001c0028a0001c0038others(1): Show | 15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
synonymous_variant | LOW | c.10977T>A | p.Ile3659Ile | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 11338/12385 | 10977/10995 | 3659/3664 | chr1 | 15939409 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15847829
|
G | C | 1 | a0001c0023t0003 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-239G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/15 | 239 | chr1 | 15847829 | |||||
chr1:15939688
|
C | G | 1 | a0003c0003t0007 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*261C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 261 | chr1 | 15939688 | |||||
chr1:15939812
|
G | A | 1 | a0011c0013t0002 | 2 | HG02886.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 385 | chr1 | 15939812 | |||||
chr1:15939858
|
C | A | 1 | a0002c0002t0004 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*431C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 431 | chr1 | 15939858 | |||||
chr1:15939938
|
T | C | 1 | a0001c0001t0005 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*511T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 511 | chr1 | 15939938 | |||||
chr1:15940413
|
T | C | 1 | a0001c0001t0006 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*986T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 986 | chr1 | 15940413 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15848166
|
C | G | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+16C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848166 | ||||||
chr1:15848218
|
G | T | 1 | a0003c0003t0001g0303 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.83+68G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848218 | ||||||
chr1:15848244
|
G | T | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+94G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848244 | ||||||
chr1:15848252
|
C | G | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.83+102C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848252 | ||||||
chr1:15848283
|
C | G | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+133C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848283 | ||||||
chr1:15848379
|
C | A | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+229C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848379 | ||||||
chr1:15848410
|
C | G | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.83+260C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848410 | ||||||
chr1:15848491
|
C | CG | 5 | a0001c0001t0005g0001a0002c0002t0001g0004a0002c0002t0001g0005others(2): Show | 5 | HG00621.hp1 HG01496.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+345dupG | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15848491 | |||||
chr1:15848510
|
G | C | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83+360G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848510 | ||||||
chr1:15848609
|
CT | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.83+461delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15848609 | |||||
chr1:15848626
|
G | C | 1 | a0020c0031t0001g0007 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.83+476G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848626 | ||||||
chr1:15848668
|
C | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+518C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848668 | ||||||
chr1:15848822
|
C | T | 106 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(103): Show | 106 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.83+672C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848822 | ||||||
chr1:15848896
|
A | C | 89 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0007t0001g0293others(86): Show | 89 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.83+746A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848896 | ||||||
chr1:15848903
|
C | G | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.83+753C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848903 | ||||||
chr1:15848947
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.83+797G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848947 | ||||||
chr1:15848958
|
C | G | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.83+808C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848958 | ||||||
chr1:15849066
|
TGTAGTGC others(10): Show |
T | 1 | a0002c0002t0001g0292 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.83+917_83+933delGT others(15): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849066 | ||||||
chr1:15849100
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.83+950C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849100 | ||||||
chr1:15849309
|
T | A | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.83+1159T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849309 | ||||||
chr1:15849436
|
T | C | 1 | a0003c0003t0001g0109 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.83+1286T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849436 | ||||||
chr1:15849556
|
G | A | 1 | a0002c0002t0001g0190 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.83+1406G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849556 | ||||||
chr1:15849622
|
G | C | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG01106.hp2 HG01884.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+1472G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849622 | ||||||
chr1:15850030
|
A | C | 1 | a0005c0005t0001g0288 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.83+1880A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850030 | ||||||
chr1:15850225
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.83+2075G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850225 | ||||||
chr1:15850226
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.83+2076C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850226 | ||||||
chr1:15850383
|
ATTCTT | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.83+2236_83+2240del others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15850383 | |||||
chr1:15850400
|
GT | G | 225 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.83+2261delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15850400 | |||||
chr1:15850475
|
G | A | 1 | a0002c0002t0001g0195 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.83+2325G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850475 | ||||||
chr1:15850489
|
G | C | 11 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(8): Show | 11 | HG01106.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.83+2339G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850489 | ||||||
chr1:15850514
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.83+2364G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850514 | ||||||
chr1:15850678
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.83+2528A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850678 | ||||||
chr1:15850688
|
A | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.83+2538A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850688 | ||||||
chr1:15850770
|
T | A | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+2620T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850770 | ||||||
chr1:15850790
|
A | G | 79 | a0001c0004t0001g0275a0002c0002t0001g0004a0002c0002t0001g0005others(76): Show | 79 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.83+2640A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850790 | ||||||
chr1:15850975
|
C | G | 1 | a0002c0002t0001g0286 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.83+2825C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850975 | ||||||
chr1:15851083
|
G | A | 216 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.83+2933G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851083 | ||||||
chr1:15851172
|
A | C | 4 | a0005c0005t0001g0210a0005c0005t0001g0211a0005c0005t0001g0212others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+3022A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851172 | ||||||
chr1:15851555
|
C | T | 1 | a0002c0002t0001g0286 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.83+3405C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851555 | ||||||
chr1:15851575
|
T | G | 2 | a0002c0002t0001g0004a0002c0002t0001g0213 | 2 | HG00621.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.83+3425T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851575 | ||||||
chr1:15851697
|
TAAAG | T | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+3549_83+3552del others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15851697 | |||||
chr1:15851760
|
G | A | 82 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(79): Show | 82 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.83+3610G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851760 | ||||||
chr1:15851768
|
A | G | 1 | a0020c0031t0001g0007 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.83+3618A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851768 | ||||||
chr1:15851937
|
C | T | 3 | a0008c0008t0001g0099a0008c0008t0001g0100a0008c0008t0001g0101 | 3 | HG01167.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.83+3787C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851937 | ||||||
chr1:15852168
|
A | C | 1 | a0004c0009t0001g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.83+4018A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852168 | ||||||
chr1:15852289
|
C | A | 1 | a0002c0002t0001g0214 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.83+4139C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852289 | ||||||
chr1:15852389
|
A | G | 1 | a0001c0015t0001g0062 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.83+4239A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852389 | ||||||
chr1:15852422
|
T | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.83+4272T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852422 | ||||||
chr1:15852613
|
T | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+4463T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852613 | ||||||
chr1:15852694
|
G | C | 4 | a0005c0005t0001g0210a0005c0005t0001g0211a0005c0005t0001g0212others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+4544G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852694 | ||||||
chr1:15852713
|
A | G | 303 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.83+4563A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852713 | ||||||
chr1:15853067
|
G | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+4917G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853067 | ||||||
chr1:15853100
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.83+4950C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853100 | ||||||
chr1:15853219
|
T | A | 1 | a0015c0021t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83+5069T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853219 | ||||||
chr1:15853290
|
A | G | 1 | a0003c0003t0001g0188 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.83+5140A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853290 | ||||||
chr1:15853668
|
A | AT | 12 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.83+5531dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15853668 | |||||
chr1:15853688
|
G | A | 1 | a0003c0003t0001g0121 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.83+5538G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853688 | ||||||
chr1:15853707
|
A | G | 1 | a0001c0001t0006g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83+5557A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853707 | ||||||
chr1:15853769
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.83+5619A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853769 | ||||||
chr1:15853858
|
G | A | 1 | a0001c0004t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.83+5708G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853858 | ||||||
chr1:15853866
|
A | G | 1 | a0002c0002t0001g0285 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.83+5716A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853866 | ||||||
chr1:15853877
|
C | T | 9 | a0003c0003t0001g0121a0003c0003t0001g0180a0003c0003t0001g0181others(6): Show | 9 | HG00423.hp1 HG00673.hp2 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+5727C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853877 | ||||||
chr1:15853912
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011 | 3 | HG00735.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.83+5762G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853912 | ||||||
chr1:15853935
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(2): Show | 5 | HG00099.hp2 HG01175.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+5785G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853935 | ||||||
chr1:15854003
|
G | A | 19 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(16): Show | 19 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.83+5853G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854003 | ||||||
chr1:15854147
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.83+5997A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854147 | ||||||
chr1:15854473
|
A | T | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+6323A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854473 | ||||||
chr1:15854509
|
C | T | 1 | a0003c0003t0001g0179 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.83+6359C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854509 | ||||||
chr1:15854544
|
A | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+6394A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854544 | ||||||
chr1:15854556
|
C | G | 1 | a0001c0026t0001g0096 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.83+6406C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854556 | ||||||
chr1:15854566
|
C | T | 7 | a0005c0005t0001g0208a0005c0005t0001g0209a0005c0005t0001g0210others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+6416C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854566 | ||||||
chr1:15854665
|
G | A | 1 | a0015c0021t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83+6515G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854665 | ||||||
chr1:15854906
|
C | G | 2 | a0003c0003t0001g0177a0003c0003t0001g0178 | 2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.83+6756C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854906 | ||||||
chr1:15855416
|
T | C | 35 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(32): Show | 35 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.83+7266T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15855416 | ||||||
chr1:15855484
|
T | C | 232 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.83+7334T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15855484 | ||||||
chr1:15855577
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.83+7427C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15855577 | ||||||
chr1:15855989
|
A | AC | 190 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.83+7840dupC | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15855989 | |||||
chr1:15855990
|
C | CCT | 36 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0037others(33): Show | 36 | HG00639.hp2 HG00735.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.83+7840_83+7841ins others(2): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15855990 | ||||||
chr1:15855991
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0198others(1): Show | 4 | HG01081.hp2 HG01167.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+7841T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15855991 | ||||||
chr1:15856016
|
G | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.83+7866G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856016 | ||||||
chr1:15856115
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.83+7965A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856115 | ||||||
chr1:15856208
|
T | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83+8058T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856208 | ||||||
chr1:15856318
|
A | G | 232 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.83+8168A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856318 | ||||||
chr1:15856535
|
T | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+8385T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856535 | ||||||
chr1:15856542
|
G | C | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+8392G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856542 | ||||||
chr1:15856558
|
C | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+8408C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856558 | ||||||
chr1:15856565
|
C | CT | 8 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0007t0001g0293others(5): Show | 8 | HG00741.hp2 HG02145.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+8435dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15856565 | |||||
chr1:15856565
|
CT | C | 158 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.83+8435delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15856565 | |||||
chr1:15856693
|
G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83+8543G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856693 | ||||||
chr1:15856749
|
A | G | 31 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(28): Show | 31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.83+8599A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856749 | ||||||
chr1:15856775
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.83+8625C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856775 | ||||||
chr1:15857050
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.83+8900C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857050 | ||||||
chr1:15857061
|
C | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.83+8911C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857061 | ||||||
chr1:15857317
|
G | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.83+9167G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857317 | ||||||
chr1:15857470
|
C | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83+9320C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857470 | ||||||
chr1:15857637
|
G | A | 106 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(103): Show | 106 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.83+9487G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857637 | ||||||
chr1:15857660
|
A | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+9510A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857660 | ||||||
chr1:15857689
|
G | GT | 213 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.83+9547dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15857689 | |||||
chr1:15857689
|
G | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.83+9539G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857689 | ||||||
chr1:15857703
|
C | T | 21 | a0001c0001t0001g0098a0001c0001t0006g0097a0001c0004t0001g0064others(18): Show | 21 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.83+9553C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857703 | ||||||
chr1:15857745
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0006g0097 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.83+9595C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857745 | ||||||
chr1:15858021
|
G | C | 2 | a0002c0002t0001g0215a0002c0002t0001g0216 | 2 | NA18941.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.83+9871G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858021 | ||||||
chr1:15858145
|
G | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(17): Show | 20 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.83+9995G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858145 | ||||||
chr1:15858252
|
C | CA | 207 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.83+10115dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15858252 | |||||
chr1:15858252
|
C | CAA | 9 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0005g0001others(6): Show | 9 | HG01074.hp2 HG02071.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+10114_83+10115d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15858252 | |||||
chr1:15858252
|
CA | C | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+10115delA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15858252 | |||||
chr1:15858481
|
A | G | 2 | a0001c0004t0001g0064a0001c0004t0001g0092 | 2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.83+10331A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858481 | ||||||
chr1:15858490
|
A | C | 1 | a0003c0003t0001g0122 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.83+10340A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858490 | ||||||
chr1:15858572
|
A | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.83+10422A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858572 | ||||||
chr1:15858628
|
T | C | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.83+10478T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858628 | ||||||
chr1:15858647
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.83+10497A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858647 | ||||||
chr1:15858658
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.83+10508A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858658 | ||||||
chr1:15858800
|
C | G | 1 | a0015c0021t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83+10650C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858800 | ||||||
chr1:15858811
|
G | T | 2 | a0001c0029t0001g0094a0019c0030t0001g0080 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.83+10661G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858811 | ||||||
chr1:15858861
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+10711T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858861 | ||||||
chr1:15858946
|
AAAAC | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+10808_83+10811d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15858946 | |||||
chr1:15858969
|
A | G | 3 | a0006c0012t0001g0103a0006c0012t0001g0104a0006c0012t0001g0105 | 3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.83+10819A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858969 | ||||||
chr1:15858997
|
A | C | 14 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(11): Show | 14 | HG01106.hp2 HG01175.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.83+10847A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858997 | ||||||
chr1:15859110
|
A | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83+10960A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859110 | ||||||
chr1:15859126
|
G | A | 1 | a0010c0016t0001g0222 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.83+10976G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859126 | ||||||
chr1:15859140
|
G | GT | 33 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.83+11006dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859140 | |||||
chr1:15859140
|
G | GTT | 170 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(167): Show | 170 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.83+11005_83+11006d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859140 | |||||
chr1:15859140
|
G | GTTT | 20 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.83+11004_83+11006d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859140 | |||||
chr1:15859140
|
G | GTTTT | 12 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.83+11003_83+11006d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859140 | |||||
chr1:15859140
|
GT | G | 11 | a0003c0003t0001g0122a0003c0003t0001g0123a0003c0003t0001g0124others(8): Show | 11 | HG01123.hp2 HG01192.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+11006delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859140 | |||||
chr1:15859260
|
A | G | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+11110A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859260 | ||||||
chr1:15859340
|
CTGTTTTC others(1): Show |
C | 3 | a0001c0004t0001g0089a0001c0004t0001g0090a0001c0004t0001g0091 | 3 | HG02486.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.83+11192_83+11199d others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859340 | |||||
chr1:15859358
|
C | CT | 126 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(123): Show | 126 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.83+11225dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859358 | |||||
chr1:15859358
|
C | CTT | 9 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0199others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+11224_83+11225d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859358 | |||||
chr1:15859358
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+11208C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859358 | ||||||
chr1:15859358
|
CT | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0301others(4): Show | 7 | HG01167.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+11225delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859358 | |||||
chr1:15859363
|
T | C | 23 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(20): Show | 23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.83+11213T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859363 | ||||||
chr1:15859396
|
C | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+11246C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859396 | ||||||
chr1:15859443
|
C | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+11293C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859443 | ||||||
chr1:15859450
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.83+11300T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859450 | ||||||
chr1:15859658
|
T | C | 1 | a0003c0003t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.83+11508T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859658 | ||||||
chr1:15859660
|
T | C | 1 | a0003c0003t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.83+11510T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859660 | ||||||
chr1:15859665
|
G | A | 1 | a0003c0003t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.83+11515G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859665 | ||||||
chr1:15859905
|
C | CTT | 12 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0014t0001g0019others(9): Show | 12 | HG00323.hp1 HG00323.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.83+11778_83+11779d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | |||||
chr1:15859905
|
C | CTTT | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.83+11777_83+11779d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | |||||
chr1:15859905
|
C | CTTTT | 31 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 31 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.83+11776_83+11779d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | |||||
chr1:15859905
|
C | CTTTTT | 47 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0037others(44): Show | 47 | HG00544.hp1 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.83+11775_83+11779d others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | |||||
chr1:15859905
|
C | CTTTTTT | 11 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(8): Show | 11 | HG00621.hp2 HG01515.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.83+11774_83+11779d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | |||||
chr1:15859905
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0006g0097a0001c0004t0001g0083a0001c0004t0001g0084others(3): Show | 6 | HG00741.hp2 HG01074.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+11772_83+11779d others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | |||||
chr1:15859905
|
C | CTTTTTTT others(3): Show |
5 | a0001c0004t0001g0086a0001c0004t0001g0091a0001c0004t0001g0095others(2): Show | 5 | HG01099.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+11770_83+11779d others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | |||||
chr1:15859905
|
C | CTTTTTTT others(4): Show |
4 | a0001c0004t0001g0064a0001c0028t0001g0088a0008c0008t0001g0099others(1): Show | 4 | HG01167.hp1 HG03225.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+11769_83+11779d others(13): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | |||||
chr1:15859905
|
C | CTTTTTTT others(5): Show |
1 | a0008c0008t0001g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.83+11768_83+11779d others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | |||||
chr1:15859942
|
T | C | 232 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.83+11792T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859942 | ||||||
chr1:15860112
|
T | C | 1 | a0001c0007t0001g0293 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83+11962T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860112 | ||||||
chr1:15860201
|
G | A | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0029t0001g0094others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+12051G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860201 | ||||||
chr1:15860227
|
G | A | 105 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(102): Show | 105 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.83+12077G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860227 | ||||||
chr1:15860378
|
G | GGT | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(90): Show | 93 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.83+12267_83+12268d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
G | GGTGT | 33 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0044others(30): Show | 33 | HG00558.hp2 HG01099.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.83+12265_83+12268d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
G | GGTGTGT | 17 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0001t0001g0290others(14): Show | 17 | HG00741.hp2 HG01243.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.83+12263_83+12268d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
G | GGTGTGTG others(1): Show |
6 | a0001c0001t0001g0057a0001c0001t0001g0298a0001c0004t0001g0084others(3): Show | 6 | HG00642.hp2 HG01516.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+12261_83+12268d others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
G | GGTGTGTG others(3): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0098 | 3 | HG00099.hp1 HG00621.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.83+12259_83+12268d others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
G | GGTGTGTG others(5): Show |
4 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0017t0001g0060others(1): Show | 4 | HG02074.hp1 HG02145.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+12257_83+12268d others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
G | GGTGTGTG others(7): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0048a0001c0017t0001g0049 | 3 | HG00544.hp1 HG03225.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.83+12255_83+12268d others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
G | GGTGTGTG others(9): Show |
1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.83+12253_83+12268d others(18): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
G | GGTGTGTG others(11): Show |
2 | a0001c0001t0001g0050a0001c0004t0001g0085 | 2 | HG03710.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.83+12251_83+12268d others(20): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
G | GGTGTGTG others(15): Show |
1 | a0015c0021t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83+12247_83+12268d others(24): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
GGT | G | 16 | a0001c0001t0001g0031a0001c0001t0001g0191a0001c0001t0001g0192others(13): Show | 16 | HG01099.hp1 HG01346.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.83+12267_83+12268d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
GGTGT | G | 17 | a0001c0001t0001g0066a0001c0001t0001g0205a0001c0001t0001g0206others(14): Show | 17 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.83+12265_83+12268d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
GGTGTGT | G | 6 | a0001c0001t0001g0196a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+12263_83+12268d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
GGTGTGTG others(1): Show |
G | 3 | a0004c0009t0001g0114a0004c0009t0001g0118a0004c0009t0001g0189 | 3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.83+12261_83+12268d others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
GGTGTGTG others(3): Show |
G | 11 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+12259_83+12268d others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860378
|
GGTGTGTG others(5): Show |
G | 1 | a0022c0020t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.83+12257_83+12268d others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | |||||
chr1:15860442
|
A | AGT | 53 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(50): Show | 53 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.83+12325_83+12326d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860442 | |||||
chr1:15860442
|
A | AGTGT | 54 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(51): Show | 54 | HG00621.hp1 HG00639.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.83+12323_83+12326d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860442 | |||||
chr1:15860442
|
A | AGTGTGT | 10 | a0001c0001t0001g0071a0001c0001t0001g0102a0001c0007t0001g0295others(7): Show | 10 | HG01891.hp1 HG02486.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+12321_83+12326d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860442 | |||||
chr1:15860442
|
AGT | A | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.83+12325_83+12326d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860442 | |||||
chr1:15860442
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.83+12317_83+12326d others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860442 | |||||
chr1:15860546
|
C | G | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-12270C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860546 | ||||||
chr1:15860548
|
T | C | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-12268T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860548 | ||||||
chr1:15860549
|
C | T | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-12267C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860549 | ||||||
chr1:15860964
|
G | C | 1 | a0003c0003t0001g0139 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.84-11852G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860964 | ||||||
chr1:15861130
|
G | A | 82 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(79): Show | 82 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.84-11686G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861130 | ||||||
chr1:15861134
|
CT | C | 8 | a0001c0001t0001g0011a0001c0004t0001g0275a0001c0014t0001g0019others(5): Show | 8 | HG00323.hp2 HG01168.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-11666delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15861134 | |||||
chr1:15861265
|
A | G | 232 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.84-11551A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861265 | ||||||
chr1:15861287
|
A | T | 1 | a0002c0002t0001g0273 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.84-11529A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861287 | ||||||
chr1:15861346
|
C | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-11470C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861346 | ||||||
chr1:15861432
|
G | C | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.84-11384G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861432 | ||||||
chr1:15861505
|
A | C | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-11311A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861505 | ||||||
chr1:15861625
|
T | C | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-11191T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861625 | ||||||
chr1:15861652
|
G | T | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.84-11164G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861652 | ||||||
chr1:15861706
|
T | G | 1 | a0002c0002t0001g0236 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.84-11110T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861706 | ||||||
chr1:15861825
|
A | T | 8 | a0005c0005t0001g0204a0005c0005t0001g0208a0005c0005t0001g0209others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-10991A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861825 | ||||||
chr1:15861850
|
G | A | 8 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-10966G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861850 | ||||||
chr1:15861964
|
C | A | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-10852C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861964 | ||||||
chr1:15861966
|
T | C | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-10850T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861966 | ||||||
chr1:15861967
|
G | T | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-10849G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861967 | ||||||
chr1:15861998
|
C | T | 1 | a0003c0003t0001g0171 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.84-10818C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861998 | ||||||
chr1:15862014
|
C | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01175.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.84-10802C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862014 | ||||||
chr1:15862060
|
A | T | 2 | a0003c0003t0001g0166a0003c0003t0001g0174 | 2 | HG02071.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.84-10756A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862060 | ||||||
chr1:15862094
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.84-10722G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862094 | ||||||
chr1:15862186
|
G | A | 216 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.84-10630G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862186 | ||||||
chr1:15862211
|
C | T | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-10605C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862211 | ||||||
chr1:15862566
|
T | C | 232 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.84-10250T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862566 | ||||||
chr1:15862766
|
C | CT | 11 | a0001c0001t0001g0056a0001c0001t0001g0301a0001c0001t0001g0302others(8): Show | 11 | HG02895.hp1 HG02897.hp2 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-10037dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15862766 | |||||
chr1:15862828
|
C | T | 31 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(28): Show | 31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.84-9988C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862828 | ||||||
chr1:15862836
|
A | G | 1 | a0002c0002t0001g0285 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.84-9980A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862836 | ||||||
chr1:15862873
|
T | A | 1 | a0002c0002t0001g0262 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.84-9943T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862873 | ||||||
chr1:15863123
|
A | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0029t0001g0094others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-9693A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863123 | ||||||
chr1:15863185
|
G | A | 1 | a0002c0002t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.84-9631G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863185 | ||||||
chr1:15863474
|
A | G | 15 | a0001c0004t0001g0064a0001c0004t0001g0081a0001c0004t0001g0083others(12): Show | 15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.84-9342A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863474 | ||||||
chr1:15863695
|
G | C | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-9121G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863695 | ||||||
chr1:15863746
|
T | TA | 23 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(20): Show | 23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.84-9069dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15863746 | |||||
chr1:15863766
|
G | C | 79 | a0001c0004t0001g0275a0002c0002t0001g0004a0002c0002t0001g0005others(76): Show | 79 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.84-9050G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863766 | ||||||
chr1:15863782
|
A | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01175.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.84-9034A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863782 | ||||||
chr1:15864105
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.84-8711A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864105 | ||||||
chr1:15864167
|
C | CT | 16 | a0003c0003t0001g0165a0003c0003t0001g0174a0003c0003t0001g0188others(13): Show | 16 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-8630dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864167 | |||||
chr1:15864167
|
CTTTTTTT others(2): Show |
C | 215 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.84-8638_84-8630del others(9): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864167 | |||||
chr1:15864231
|
C | T | 23 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(20): Show | 23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.84-8585C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864231 | ||||||
chr1:15864293
|
C | T | 2 | a0001c0001t0001g0196a0001c0037t0001g0197 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.84-8523C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864293 | ||||||
chr1:15864419
|
C | T | 8 | a0005c0005t0001g0204a0005c0005t0001g0208a0005c0005t0001g0209others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-8397C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864419 | ||||||
chr1:15864470
|
G | GT | 76 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0037others(73): Show | 76 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.84-8327dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864470 | |||||
chr1:15864470
|
G | GTT | 50 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.84-8328_84-8327dup others(2): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864470 | |||||
chr1:15864470
|
GT | G | 9 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(6): Show | 9 | HG01168.hp2 HG01256.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.84-8327delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864470 | |||||
chr1:15864474
|
T | TG | 14 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(11): Show | 14 | HG01106.hp2 HG01175.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.84-8342_84-8341ins others(1): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864474 | ||||||
chr1:15864489
|
T | A | 1 | a0004c0006t0001g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.84-8327T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864489 | ||||||
chr1:15864607
|
G | GT | 20 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0020others(17): Show | 20 | HG00544.hp2 HG00639.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.84-8188dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864607 | |||||
chr1:15864607
|
GT | G | 171 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0037others(168): Show | 171 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.84-8188delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864607 | |||||
chr1:15864717
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.84-8099G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864717 | ||||||
chr1:15864752
|
C | T | 31 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(28): Show | 31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.84-8064C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864752 | ||||||
chr1:15864867
|
G | C | 1 | a0005c0005t0001g0204 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.84-7949G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864867 | ||||||
chr1:15864886
|
G | A | 1 | a0001c0026t0001g0096 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.84-7930G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864886 | ||||||
chr1:15865024
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.84-7792T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865024 | ||||||
chr1:15865050
|
CTTAATT | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(18): Show | 21 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.84-7757_84-7752del others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15865050 | |||||
chr1:15865213
|
G | A | 1 | a0001c0029t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.84-7603G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865213 | ||||||
chr1:15865242
|
G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-7574G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865242 | ||||||
chr1:15865264
|
A | G | 232 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.84-7552A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865264 | ||||||
chr1:15865420
|
G | GT | 30 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0070others(27): Show | 30 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.84-7377dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15865420 | |||||
chr1:15865420
|
GT | G | 105 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(102): Show | 105 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.84-7377delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15865420 | |||||
chr1:15865472
|
G | C | 1 | a0002c0018t0001g0276 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.84-7344G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865472 | ||||||
chr1:15865584
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.84-7232G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865584 | ||||||
chr1:15865701
|
CAGGT | C | 106 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(103): Show | 106 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.84-7114_84-7111del others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865701 | ||||||
chr1:15865722
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.84-7094A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865722 | ||||||
chr1:15865785
|
G | A | 7 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0045others(4): Show | 7 | HG00099.hp1 HG00642.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-7031G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865785 | ||||||
chr1:15865868
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.84-6948G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865868 | ||||||
chr1:15865889
|
T | G | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-6927T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865889 | ||||||
chr1:15865895
|
T | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-6921T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865895 | ||||||
chr1:15865899
|
A | G | 232 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.84-6917A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865899 | ||||||
chr1:15866385
|
ACT | A | 3 | a0005c0005t0001g0208a0005c0005t0001g0209a0005c0005t0001g0288 | 3 | HG01069.hp2 HG01071.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.84-6428_84-6427del others(2): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15866385 | |||||
chr1:15866423
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.84-6393G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866423 | ||||||
chr1:15866446
|
C | T | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-6370C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866446 | ||||||
chr1:15866555
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.84-6261A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866555 | ||||||
chr1:15866829
|
A | T | 1 | a0003c0003t0001g0123 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.84-5987A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866829 | ||||||
chr1:15866830
|
T | G | 1 | a0003c0003t0001g0123 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.84-5986T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866830 | ||||||
chr1:15866831
|
G | C | 1 | a0003c0003t0001g0123 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.84-5985G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866831 | ||||||
chr1:15866994
|
A | T | 1 | a0001c0004t0001g0086 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.84-5822A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866994 | ||||||
chr1:15867052
|
T | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-5764T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15867052 | ||||||
chr1:15867502
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.84-5314C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15867502 | ||||||
chr1:15867710
|
G | C | 1 | a0003c0003t0001g0177 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.84-5106G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15867710 | ||||||
chr1:15867712
|
C | CT | 6 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0079others(3): Show | 6 | HG00099.hp1 HG01346.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.84-5090dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15867712 | |||||
chr1:15867713
|
T | C | 1 | a0003c0003t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.84-5103T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15867713 | ||||||
chr1:15867812
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-5004C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15867812 | ||||||
chr1:15868163
|
T | A | 25 | a0001c0001t0001g0098a0001c0001t0001g0299a0001c0001t0001g0300others(22): Show | 25 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.84-4653T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868163 | ||||||
chr1:15868438
|
C | CT | 30 | a0001c0001t0001g0098a0001c0001t0001g0298a0001c0001t0001g0299others(27): Show | 30 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.84-4364dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15868438 | |||||
chr1:15868506
|
C | T | 2 | a0001c0029t0001g0094a0019c0030t0001g0080 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.84-4310C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868506 | ||||||
chr1:15868527
|
C | T | 1 | a0003c0003t0001g0163 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.84-4289C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868527 | ||||||
chr1:15868623
|
A | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-4193A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868623 | ||||||
chr1:15868714
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.84-4102G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868714 | ||||||
chr1:15868764
|
C | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-4052C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868764 | ||||||
chr1:15868980
|
T | G | 1 | a0002c0002t0001g0239 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.84-3836T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868980 | ||||||
chr1:15869155
|
C | T | 2 | a0001c0029t0001g0094a0019c0030t0001g0080 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.84-3661C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15869155 | ||||||
chr1:15869232
|
G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-3584G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15869232 | ||||||
chr1:15869352
|
G | A | 13 | a0003c0003t0001g0124a0003c0003t0001g0139a0003c0003t0001g0140others(10): Show | 13 | HG00423.hp2 NA18612.hp2 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.84-3464G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15869352 | ||||||
chr1:15869380
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0021others(4): Show | 7 | HG00639.hp1 HG01081.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-3436G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15869380 | ||||||
chr1:15869580
|
G | GTATT | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(70): Show | 73 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.84-3204_84-3201dup others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15869580 | |||||
chr1:15869580
|
G | GTATTTAT others(1): Show |
99 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0070others(96): Show | 99 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.84-3208_84-3201dup others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15869580 | |||||
chr1:15869580
|
G | GTATTTAT others(5): Show |
16 | a0001c0001t0001g0192a0001c0001t0001g0202a0001c0004t0001g0064others(13): Show | 16 | HG00323.hp1 HG01934.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-3212_84-3201dup others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15869580 | |||||
chr1:15869580
|
G | GTATTTAT others(9): Show |
2 | a0001c0038t0001g0093a0002c0002t0001g0250 | 2 | HG00741.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.84-3216_84-3201dup others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15869580 | |||||
chr1:15869989
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.84-2827C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15869989 | ||||||
chr1:15870023
|
C | G | 2 | a0001c0004t0001g0081a0002c0002t0001g0082 | 2 | NA18952.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.84-2793C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870023 | ||||||
chr1:15870058
|
G | A | 2 | a0011c0013t0002g0054a0011c0013t0002g0055 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.84-2758G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870058 | ||||||
chr1:15870122
|
G | C | 1 | a0002c0002t0001g0253 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.84-2694G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870122 | ||||||
chr1:15870217
|
A | C | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-2599A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870217 | ||||||
chr1:15870240
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.84-2576A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870240 | ||||||
chr1:15870253
|
T | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.84-2563T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870253 | ||||||
chr1:15870264
|
A | G | 106 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(103): Show | 106 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.84-2552A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870264 | ||||||
chr1:15870304
|
G | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.84-2512G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870304 | ||||||
chr1:15870752
|
A | AAGG | 303 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.84-2061_84-2059dup others(3): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15870752 | |||||
chr1:15870901
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-1915C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870901 | ||||||
chr1:15871086
|
A | C | 19 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(16): Show | 19 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.84-1730A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871086 | ||||||
chr1:15871260
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.84-1556G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871260 | ||||||
chr1:15871443
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.84-1373C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871443 | ||||||
chr1:15871524
|
G | T | 1 | a0001c0007t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.84-1292G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871524 | ||||||
chr1:15871563
|
G | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-1253G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871563 | ||||||
chr1:15871747
|
A | C | 1 | a0001c0028t0001g0088 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.84-1069A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871747 | ||||||
chr1:15871917
|
A | G | 2 | a0001c0004t0001g0089a0001c0004t0001g0091 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.84-899A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871917 | ||||||
chr1:15871939
|
G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-877G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871939 | ||||||
chr1:15872145
|
C | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-671C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872145 | ||||||
chr1:15872189
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0006g0097 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.84-627C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872189 | ||||||
chr1:15872222
|
C | CA | 14 | a0001c0001t0001g0029a0001c0001t0001g0199a0001c0001t0001g0202others(11): Show | 14 | HG01109.hp2 HG02040.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.84-572dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15872222 | |||||
chr1:15872222
|
CA | C | 82 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0036others(79): Show | 82 | HG00544.hp1 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.84-572delA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15872222 | |||||
chr1:15872222
|
CAA | C | 8 | a0001c0001t0001g0075a0001c0001t0001g0102a0001c0004t0001g0084others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-573_84-572delAA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15872222 | |||||
chr1:15872318
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.84-498C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872318 | ||||||
chr1:15872320
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.84-496C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872320 | ||||||
chr1:15872359
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0005g0001 | 3 | HG03041.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.84-457A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872359 | ||||||
chr1:15872369
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-447G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872369 | ||||||
chr1:15872462
|
T | C | 1 | a0002c0002t0001g0262 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.84-354T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872462 | ||||||
chr1:15872556
|
T | C | 232 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.84-260T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872556 | ||||||
chr1:15872558
|
C | T | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.84-258C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872558 | ||||||
chr1:15872587
|
G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-229G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872587 | ||||||
chr1:15872599
|
C | CA | 22 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0045others(19): Show | 22 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.84-201dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15872599 | |||||
chr1:15872599
|
CAAAAA | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.84-205_84-201delAA others(3): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15872599 | |||||
chr1:15872661
|
G | A | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-155G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872661 | ||||||
chr1:15872664
|
A | C | 1 | a0002c0002t0001g0272 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.84-152A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872664 | ||||||
chr1:15873269
|
G | A | 1 | a0003c0003t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.404+133G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15873269 | ||||||
chr1:15873668
|
A | G | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.404+532A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15873668 | ||||||
chr1:15873734
|
C | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404+598C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15873734 | ||||||
chr1:15873896
|
A | G | 1 | a0003c0003t0001g0167 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.404+760A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15873896 | ||||||
chr1:15874769
|
G | A | 2 | a0001c0014t0001g0019a0001c0014t0001g0034 | 2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.405-1433G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15874769 | ||||||
chr1:15874845
|
T | C | 14 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(11): Show | 14 | HG01106.hp2 HG01175.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.405-1357T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15874845 | ||||||
chr1:15874980
|
T | C | 8 | a0005c0005t0001g0204a0005c0005t0001g0208a0005c0005t0001g0209others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-1222T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15874980 | ||||||
chr1:15875007
|
G | T | 29 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(26): Show | 29 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.405-1195G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875007 | ||||||
chr1:15875169
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.405-1033G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875169 | ||||||
chr1:15875217
|
C | T | 4 | a0002c0002t0001g0227a0002c0002t0001g0233a0002c0002t0001g0251others(1): Show | 4 | HG00323.hp1 HG01074.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-985C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875217 | ||||||
chr1:15875218
|
G | A | 4 | a0001c0017t0001g0049a0001c0017t0001g0060a0001c0029t0001g0094others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-984G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875218 | ||||||
chr1:15875264
|
T | A | 1 | a0003c0003t0007g0162 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.405-938T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875264 | ||||||
chr1:15875280
|
T | TTTTAA | 232 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.405-920_405-919ins others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 15875280 | |||||
chr1:15875399
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0006g0097 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.405-803A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875399 | ||||||
chr1:15875440
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.405-762G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875440 | ||||||
chr1:15875678
|
A | T | 4 | a0005c0005t0001g0210a0005c0005t0001g0211a0005c0005t0001g0212others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-524A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875678 | ||||||
chr1:15875709
|
C | A | 43 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(40): Show | 43 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.405-493C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875709 | ||||||
chr1:15875905
|
G | A | 1 | a0002c0002t0001g0247 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.405-297G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875905 | ||||||
chr1:15875947
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-255G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875947 | ||||||
chr1:15876852
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+174G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15876852 | ||||||
chr1:15876980
|
T | C | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+302T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15876980 | ||||||
chr1:15877027
|
T | C | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+349T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877027 | ||||||
chr1:15877044
|
T | C | 8 | a0005c0005t0001g0204a0005c0005t0001g0208a0005c0005t0001g0209others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.881+366T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877044 | ||||||
chr1:15877168
|
G | T | 2 | a0001c0001t0001g0098a0001c0001t0006g0097 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.881+490G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877168 | ||||||
chr1:15877198
|
C | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.881+520C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877198 | ||||||
chr1:15877261
|
C | G | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+583C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877261 | ||||||
chr1:15877309
|
C | T | 2 | a0002c0002t0001g0215a0002c0002t0001g0216 | 2 | NA18941.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.881+631C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877309 | ||||||
chr1:15877345
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.881+667G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877345 | ||||||
chr1:15877738
|
C | CT | 31 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0059others(28): Show | 31 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.881+1083dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15877738 | |||||
chr1:15877738
|
C | CTT | 7 | a0001c0001t0001g0079a0001c0001t0001g0098a0001c0001t0006g0097others(4): Show | 7 | HG01243.hp2 HG02647.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.881+1082_881+1083d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15877738 | |||||
chr1:15877738
|
CT | C | 16 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(13): Show | 16 | HG01070.hp1 HG01071.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.881+1083delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15877738 | |||||
chr1:15877795
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.881+1117A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877795 | ||||||
chr1:15878006
|
G | A | 22 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(19): Show | 22 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.881+1328G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878006 | ||||||
chr1:15878070
|
C | G | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.881+1392C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878070 | ||||||
chr1:15878170
|
A | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+1492A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878170 | ||||||
chr1:15878252
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0028 | 2 | HG00280.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.881+1574A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878252 | ||||||
chr1:15878293
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.881+1615A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878293 | ||||||
chr1:15878488
|
G | A | 1 | a0002c0002t0001g0264 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.881+1810G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878488 | ||||||
chr1:15878581
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.881+1903C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878581 | ||||||
chr1:15878607
|
T | C | 216 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.881+1929T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878607 | ||||||
chr1:15878708
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.881+2030T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878708 | ||||||
chr1:15878747
|
C | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+2069C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878747 | ||||||
chr1:15878802
|
G | C | 1 | a0002c0002t0001g0240 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.881+2124G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878802 | ||||||
chr1:15878907
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.881+2229G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878907 | ||||||
chr1:15879004
|
CA | C | 25 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0031others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.881+2346delA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879004 | |||||
chr1:15879004
|
CAA | C | 207 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.881+2345_881+2346d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879004 | |||||
chr1:15879004
|
CAAA | C | 7 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0205others(4): Show | 7 | HG01175.hp2 HG01516.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.881+2344_881+2346d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879004 | |||||
chr1:15879109
|
T | TG | 16 | a0001c0004t0001g0064a0001c0004t0001g0081a0001c0004t0001g0083others(13): Show | 16 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.881+2434dupG | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879109 | |||||
chr1:15879256
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.881+2578G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879256 | ||||||
chr1:15879483
|
C | T | 2 | a0003c0003t0001g0109a0003c0003t0001g0165 | 2 | HG00558.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.881+2805C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879483 | ||||||
chr1:15879675
|
A | AT | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.881+3010dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879675 | |||||
chr1:15879675
|
AT | A | 12 | a0001c0001t0001g0198a0004c0006t0001g0002a0004c0006t0001g0111others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.881+3010delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879675 | |||||
chr1:15879693
|
C | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+3015C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879693 | ||||||
chr1:15879770
|
A | G | 1 | a0002c0002t0001g0264 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.881+3092A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879770 | ||||||
chr1:15879922
|
G | A | 1 | a0003c0003t0001g0188 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.881+3244G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879922 | ||||||
chr1:15879961
|
C | T | 1 | a0001c0004t0001g0090 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.881+3283C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879961 | ||||||
chr1:15879962
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.881+3284G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879962 | ||||||
chr1:15880007
|
A | C | 1 | a0002c0002t0001g0213 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.881+3329A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880007 | ||||||
chr1:15880062
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033 | 3 | HG01243.hp1 HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.881+3384T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880062 | ||||||
chr1:15880336
|
C | T | 1 | a0002c0002t0001g0278 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.881+3658C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880336 | ||||||
chr1:15880453
|
C | CT | 43 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 43 | HG00099.hp2 HG00673.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.881+3797dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15880453 | |||||
chr1:15880453
|
C | CTT | 17 | a0001c0001t0001g0045a0001c0001t0001g0098a0001c0001t0006g0097others(14): Show | 17 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.881+3796_881+3797d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15880453 | |||||
chr1:15880453
|
CT | C | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025others(13): Show | 16 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.881+3797delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15880453 | |||||
chr1:15880544
|
C | T | 1 | a0004c0009t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.881+3866C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880544 | ||||||
chr1:15880676
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0006g0097 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.881+3998C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880676 | ||||||
chr1:15880811
|
T | C | 1 | a0001c0004t0001g0084 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.881+4133T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880811 | ||||||
chr1:15880976
|
C | T | 1 | a0003c0003t0001g0157 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.881+4298C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880976 | ||||||
chr1:15881193
|
C | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+4515C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15881193 | ||||||
chr1:15881208
|
G | C | 31 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(28): Show | 31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.881+4530G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15881208 | ||||||
chr1:15881367
|
T | G | 23 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(20): Show | 23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.881+4689T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15881367 | ||||||
chr1:15881497
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.881+4819A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15881497 | ||||||
chr1:15881768
|
G | A | 1 | a0003c0003t0001g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.881+5090G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15881768 | ||||||
chr1:15882109
|
T | C | 228 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.881+5431T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882109 | ||||||
chr1:15882138
|
T | A | 232 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.881+5460T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882138 | ||||||
chr1:15882384
|
A | G | 1 | a0001c0004t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.881+5706A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882384 | ||||||
chr1:15882385
|
G | A | 1 | a0003c0003t0001g0154 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.881+5707G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882385 | ||||||
chr1:15882422
|
G | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.881+5744G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882422 | ||||||
chr1:15882433
|
G | A | 21 | a0001c0001t0001g0098a0001c0001t0006g0097a0001c0004t0001g0064others(18): Show | 21 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.881+5755G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882433 | ||||||
chr1:15882636
|
G | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+5958G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882636 | ||||||
chr1:15882717
|
G | T | 2 | a0003c0003t0001g0166a0003c0003t0001g0174 | 2 | HG02071.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.881+6039G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882717 | ||||||
chr1:15882915
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01175.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.881+6237C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882915 | ||||||
chr1:15883112
|
A | T | 23 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(20): Show | 23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.881+6434A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883112 | ||||||
chr1:15883365
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+6687G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883365 | ||||||
chr1:15883516
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+6838G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883516 | ||||||
chr1:15883546
|
G | A | 1 | a0002c0002t0001g0213 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.881+6868G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883546 | ||||||
chr1:15883572
|
C | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+6894C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883572 | ||||||
chr1:15883617
|
G | A | 1 | a0002c0002t0001g0221 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.881+6939G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883617 | ||||||
chr1:15883675
|
T | C | 1 | a0001c0004t0001g0086 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.881+6997T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883675 | ||||||
chr1:15883715
|
AT | A | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+7046delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15883715 | |||||
chr1:15883807
|
CT | C | 221 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.881+7149delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15883807 | |||||
chr1:15883807
|
CTT | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0036others(4): Show | 7 | HG01109.hp1 HG01168.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.881+7148_881+7149d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15883807 | |||||
chr1:15883848
|
C | T | 1 | a0019c0030t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.881+7170C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883848 | ||||||
chr1:15883862
|
T | G | 1 | a0001c0015t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.881+7184T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883862 | ||||||
chr1:15883878
|
C | T | 216 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.881+7200C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883878 | ||||||
chr1:15883937
|
G | A | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+7259G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883937 | ||||||
chr1:15883941
|
C | G | 1 | a0003c0003t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.881+7263C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883941 | ||||||
chr1:15884056
|
C | T | 2 | a0011c0013t0002g0054a0011c0013t0002g0055 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.881+7378C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884056 | ||||||
chr1:15884505
|
T | C | 2 | a0002c0002t0001g0280a0002c0002t0001g0283 | 2 | NA18953.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.881+7827T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884505 | ||||||
chr1:15884520
|
A | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+7842A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884520 | ||||||
chr1:15884701
|
C | CTTTCCT | 3 | a0001c0001t0001g0075a0001c0001t0001g0102a0001c0027t0001g0076 | 3 | HG01891.hp1 HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.881+8039_881+8044d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15884701 | |||||
chr1:15884739
|
CT | C | 233 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.881+8073delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15884739 | |||||
chr1:15884743
|
T | C | 9 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(6): Show | 9 | HG01123.hp2 HG01192.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.881+8065T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884743 | ||||||
chr1:15884770
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.881+8092C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884770 | ||||||
chr1:15884778
|
G | T | 1 | a0003c0003t0001g0303 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.881+8100G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884778 | ||||||
chr1:15884782
|
A | G | 228 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.881+8104A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884782 | ||||||
chr1:15884816
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.881+8138C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884816 | ||||||
chr1:15884889
|
C | G | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.881+8211C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884889 | ||||||
chr1:15884984
|
G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+8306G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884984 | ||||||
chr1:15885232
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.881+8554C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885232 | ||||||
chr1:15885323
|
C | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+8645C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885323 | ||||||
chr1:15885396
|
C | G | 1 | a0003c0003t0001g0126 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.881+8718C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885396 | ||||||
chr1:15885447
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+8769C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885447 | ||||||
chr1:15885696
|
C | G | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+9018C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885696 | ||||||
chr1:15885724
|
G | T | 15 | a0001c0004t0001g0064a0001c0004t0001g0081a0001c0004t0001g0083others(12): Show | 15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.881+9046G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885724 | ||||||
chr1:15885810
|
C | CT | 4 | a0005c0005t0001g0210a0005c0005t0001g0211a0005c0005t0001g0212others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+9139dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15885810 | |||||
chr1:15885810
|
C | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+9132C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885810 | ||||||
chr1:15885999
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+9321G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885999 | ||||||
chr1:15886011
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.881+9333C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886011 | ||||||
chr1:15886140
|
T | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+9462T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886140 | ||||||
chr1:15886244
|
G | A | 224 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.881+9566G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886244 | ||||||
chr1:15886415
|
C | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+9737C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886415 | ||||||
chr1:15886494
|
G | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG01106.hp2 HG01884.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+9816G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886494 | ||||||
chr1:15886792
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+10114G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886792 | ||||||
chr1:15887018
|
G | A | 75 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.881+10340G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887018 | ||||||
chr1:15887108
|
T | G | 1 | a0002c0002t0001g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.881+10430T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887108 | ||||||
chr1:15887276
|
A | AT | 120 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(117): Show | 120 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.881+10620dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15887276 | |||||
chr1:15887276
|
A | ATT | 87 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.881+10619_881+1062 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15887276 | |||||
chr1:15887276
|
A | ATTT | 17 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0050others(14): Show | 17 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.881+10618_881+1062 others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15887276 | |||||
chr1:15887373
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.881+10695C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887373 | ||||||
chr1:15887575
|
G | T | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+10897G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887575 | ||||||
chr1:15887590
|
T | A | 2 | a0003c0003t0001g0144a0003c0003t0001g0145 | 2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.881+10912T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887590 | ||||||
chr1:15887653
|
T | C | 2 | a0002c0002t0001g0280a0002c0002t0001g0283 | 2 | NA18953.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.881+10975T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887653 | ||||||
chr1:15887720
|
T | TA | 7 | a0001c0004t0001g0081a0001c0004t0001g0083a0001c0004t0001g0084others(4): Show | 7 | HG00741.hp2 HG01074.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.881+11055dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15887720 | |||||
chr1:15888322
|
T | A | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+11644T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888322 | ||||||
chr1:15888326
|
TTTA | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+11654_881+1165 others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15888326 | |||||
chr1:15888481
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.881+11803G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888481 | ||||||
chr1:15888711
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.881+12033C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888711 | ||||||
chr1:15888757
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.881+12079G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888757 | ||||||
chr1:15888841
|
G | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.881+12163G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888841 | ||||||
chr1:15888958
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.881+12280C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888958 | ||||||
chr1:15889113
|
G | C | 197 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.881+12435G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889113 | ||||||
chr1:15889164
|
C | CT | 173 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.881+12502dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15889164 | |||||
chr1:15889164
|
C | CTT | 35 | a0001c0001t0001g0077a0001c0001t0001g0098a0001c0001t0001g0191others(32): Show | 35 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.881+12501_881+1250 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15889164 | |||||
chr1:15889170
|
T | C | 1 | a0002c0002t0001g0282 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.881+12492T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889170 | ||||||
chr1:15889424
|
C | T | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.881+12746C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889424 | ||||||
chr1:15889457
|
T | C | 197 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.881+12779T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889457 | ||||||
chr1:15889608
|
A | G | 1 | a0002c0002t0001g0261 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.881+12930A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889608 | ||||||
chr1:15889928
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.881+13250T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889928 | ||||||
chr1:15889983
|
G | A | 15 | a0001c0004t0001g0064a0001c0004t0001g0081a0001c0004t0001g0083others(12): Show | 15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.881+13305G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889983 | ||||||
chr1:15890008
|
C | T | 1 | a0003c0003t0001g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.881+13330C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890008 | ||||||
chr1:15890123
|
T | A | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.881+13445T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890123 | ||||||
chr1:15890148
|
A | G | 1 | a0004c0009t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.881+13470A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890148 | ||||||
chr1:15890207
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.881+13529A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890207 | ||||||
chr1:15890389
|
A | C | 1 | a0001c0004t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.881+13711A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890389 | ||||||
chr1:15890556
|
AG | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0014t0001g0019 | 3 | HG00323.hp2 HG01515.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.881+13880delG | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15890556 | |||||
chr1:15890558
|
G | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.881+13880G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890558 | ||||||
chr1:15890558
|
G | GT | 11 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0079others(8): Show | 11 | HG02486.hp1 HG02572.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.881+13902dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15890558 | |||||
chr1:15890558
|
G | GTTT | 8 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.881+13900_881+1390 others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15890558 | |||||
chr1:15890558
|
GT | G | 10 | a0001c0001t0001g0042a0001c0037t0001g0197a0002c0002t0001g0241others(7): Show | 10 | HG00099.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.881+13902delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15890558 | |||||
chr1:15890559
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0014t0001g0019 | 3 | HG00323.hp2 HG01515.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.881+13881T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890559 | ||||||
chr1:15890712
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+14034C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890712 | ||||||
chr1:15890870
|
C | T | 1 | a0002c0002t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.881+14192C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890870 | ||||||
chr1:15890916
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+14238C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890916 | ||||||
chr1:15890999
|
G | A | 2 | a0002c0002t0001g0231a0002c0002t0001g0242 | 2 | HG03490.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.881+14321G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890999 | ||||||
chr1:15891216
|
T | C | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.881+14538T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891216 | ||||||
chr1:15891270
|
T | C | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.881+14592T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891270 | ||||||
chr1:15891352
|
A | AT | 24 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(21): Show | 24 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.881+14691dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15891352 | |||||
chr1:15891403
|
G | T | 1 | a0001c0029t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.881+14725G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891403 | ||||||
chr1:15891435
|
T | G | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+14757T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891435 | ||||||
chr1:15891476
|
C | T | 1 | a0001c0017t0001g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.881+14798C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891476 | ||||||
chr1:15891601
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.881+14923C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891601 | ||||||
chr1:15891694
|
T | C | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.881+15016T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891694 | ||||||
chr1:15891777
|
G | T | 2 | a0001c0014t0001g0019a0001c0014t0001g0034 | 2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.881+15099G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891777 | ||||||
chr1:15891786
|
G | A | 1 | a0002c0002t0001g0256 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.881+15108G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891786 | ||||||
chr1:15891794
|
A | G | 2 | a0001c0015t0001g0046a0001c0015t0001g0062 | 2 | HG02132.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.881+15116A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891794 | ||||||
chr1:15891899
|
G | GT | 4 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0005g0001others(1): Show | 4 | HG01168.hp2 HG03041.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+15228dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15891899 | |||||
chr1:15891906
|
T | A | 1 | a0001c0001t0001g0028 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.881+15228T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891906 | ||||||
chr1:15891906
|
T | TA | 81 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0298others(78): Show | 81 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.881+15240dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15891906 | |||||
chr1:15891907
|
A | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0203a0001c0014t0001g0034others(1): Show | 4 | HG01069.hp1 HG01106.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+15229A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891907 | ||||||
chr1:15892012
|
C | CT | 9 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0001g0108others(6): Show | 9 | HG00639.hp2 HG00741.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.881+15359dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | |||||
chr1:15892012
|
C | CTT | 10 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.881+15358_881+1535 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | |||||
chr1:15892012
|
CT | C | 138 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.881+15359delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | |||||
chr1:15892012
|
CTTTTTTT | C | 71 | a0001c0001t0001g0106a0001c0029t0001g0094a0003c0003t0001g0109others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.881+15353_881+1535 others(11): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | |||||
chr1:15892012
|
CTTTTTTT others(3): Show |
C | 1 | a0021c0032t0001g0087 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.881+15350_881+1535 others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | |||||
chr1:15892012
|
CTTTTTTT others(5): Show |
C | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+15348_881+1535 others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | |||||
chr1:15892071
|
A | C | 3 | a0001c0004t0001g0083a0001c0004t0001g0084a0001c0038t0001g0093 | 3 | HG00741.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.881+15393A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15892071 | ||||||
chr1:15892240
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.881+15562G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15892240 | ||||||
chr1:15892328
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.881+15650G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15892328 | ||||||
chr1:15892361
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.881+15683T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15892361 | ||||||
chr1:15892991
|
A | G | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+16313A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15892991 | ||||||
chr1:15893025
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.882-16296G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893025 | ||||||
chr1:15893055
|
G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-16266G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893055 | ||||||
chr1:15893114
|
C | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-16207C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893114 | ||||||
chr1:15893342
|
G | A | 1 | a0002c0002t0001g0256 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.882-15979G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893342 | ||||||
chr1:15893623
|
G | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.882-15698G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893623 | ||||||
chr1:15893825
|
G | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.882-15496G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893825 | ||||||
chr1:15893979
|
A | G | 15 | a0001c0004t0001g0064a0001c0004t0001g0081a0001c0004t0001g0083others(12): Show | 15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.882-15342A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893979 | ||||||
chr1:15894024
|
A | G | 1 | a0002c0002t0001g0282 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.882-15297A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894024 | ||||||
chr1:15894121
|
G | C | 1 | a0004c0009t0001g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.882-15200G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894121 | ||||||
chr1:15894533
|
G | GTTTTTTT others(3): Show |
3 | a0004c0006t0001g0111a0004c0006t0001g0113a0004c0009t0001g0118 | 3 | HG01071.hp2 HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.882-14786_882-1478 others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15894533 | |||||
chr1:15894535
|
T | G | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-14786T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894535 | ||||||
chr1:15894535
|
T | TG | 3 | a0005c0005t0001g0208a0005c0005t0001g0209a0005c0005t0001g0288 | 3 | HG01069.hp2 HG01071.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.882-14785dupG | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15894535 | |||||
chr1:15894536
|
G | GT | 80 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(77): Show | 80 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.882-14762dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15894536 | |||||
chr1:15894536
|
G | GTT | 6 | a0001c0001t0001g0053a0001c0001t0001g0077a0001c0001t0001g0196others(3): Show | 6 | HG03453.hp1 HG04115.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.882-14763_882-1476 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15894536 | |||||
chr1:15894536
|
G | T | 10 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-14785G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894536 | ||||||
chr1:15894545
|
T | G | 1 | a0001c0029t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.882-14776T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894545 | ||||||
chr1:15894690
|
G | A | 1 | a0001c0026t0001g0096 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.882-14631G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894690 | ||||||
chr1:15894860
|
A | C | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-14461A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894860 | ||||||
chr1:15895123
|
T | G | 2 | a0001c0014t0001g0019a0001c0014t0001g0034 | 2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.882-14198T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895123 | ||||||
chr1:15895238
|
T | G | 4 | a0002c0002t0001g0227a0002c0002t0001g0233a0002c0002t0001g0251others(1): Show | 4 | HG00323.hp1 HG01074.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-14083T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895238 | ||||||
chr1:15895288
|
A | C | 1 | a0006c0012t0001g0104 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.882-14033A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895288 | ||||||
chr1:15895319
|
C | G | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.882-14002C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895319 | ||||||
chr1:15895414
|
A | C | 1 | a0004c0009t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.882-13907A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895414 | ||||||
chr1:15895678
|
C | CT | 46 | a0001c0001t0001g0106a0001c0001t0001g0299a0001c0001t0001g0300others(43): Show | 46 | HG00558.hp2 HG00741.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.882-13624dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15895678 | |||||
chr1:15895678
|
CT | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0298others(5): Show | 8 | HG00642.hp2 HG00673.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.882-13624delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15895678 | |||||
chr1:15895708
|
T | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-13613T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895708 | ||||||
chr1:15895734
|
G | T | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882-13587G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895734 | ||||||
chr1:15895772
|
C | T | 6 | a0002c0002t0001g0235a0002c0002t0001g0257a0002c0002t0001g0258others(3): Show | 6 | NA18971.hp2 NA19005.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.882-13549C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895772 | ||||||
chr1:15895847
|
T | A | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-13474T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895847 | ||||||
chr1:15896099
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882-13222T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896099 | ||||||
chr1:15896187
|
C | CT | 23 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0032others(20): Show | 23 | HG00099.hp2 HG00621.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.882-13106dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15896187 | |||||
chr1:15896187
|
CT | C | 38 | a0001c0001t0001g0022a0001c0001t0001g0191a0001c0001t0001g0192others(35): Show | 38 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.882-13106delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15896187 | |||||
chr1:15896187
|
CTT | C | 42 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0078others(39): Show | 42 | HG00642.hp2 HG01071.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.882-13107_882-1310 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15896187 | |||||
chr1:15896187
|
CTTT | C | 89 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(86): Show | 89 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.882-13108_882-1310 others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15896187 | |||||
chr1:15896318
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.882-13003C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896318 | ||||||
chr1:15896332
|
A | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033 | 3 | HG01243.hp1 HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.882-12989A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896332 | ||||||
chr1:15896424
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882-12897G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896424 | ||||||
chr1:15896509
|
T | C | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-12812T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896509 | ||||||
chr1:15896582
|
A | G | 1 | a0009c0011t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.882-12739A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896582 | ||||||
chr1:15896728
|
A | G | 2 | a0003c0003t0001g0109a0003c0003t0001g0165 | 2 | HG00558.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.882-12593A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896728 | ||||||
chr1:15896826
|
G | C | 1 | a0002c0002t0001g0268 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.882-12495G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896826 | ||||||
chr1:15896836
|
C | T | 87 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(84): Show | 87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.882-12485C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896836 | ||||||
chr1:15896879
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.882-12442G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896879 | ||||||
chr1:15896893
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0006g0097 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.882-12428A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896893 | ||||||
chr1:15897181
|
G | T | 1 | a0002c0002t0001g0261 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.882-12140G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897181 | ||||||
chr1:15897200
|
G | T | 197 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.882-12121G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897200 | ||||||
chr1:15897314
|
G | A | 1 | a0003c0003t0001g0131 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.882-12007G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897314 | ||||||
chr1:15897345
|
T | C | 224 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.882-11976T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897345 | ||||||
chr1:15897365
|
CT | C | 8 | a0005c0005t0001g0204a0005c0005t0001g0208a0005c0005t0001g0209others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-11942delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15897365 | |||||
chr1:15897642
|
G | A | 1 | a0003c0003t0001g0147 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.882-11679G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897642 | ||||||
chr1:15897673
|
T | A | 3 | a0001c0004t0001g0089a0001c0004t0001g0090a0001c0004t0001g0091 | 3 | HG02486.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.882-11648T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897673 | ||||||
chr1:15897845
|
T | G | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.882-11476T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897845 | ||||||
chr1:15898002
|
T | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.882-11319T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898002 | ||||||
chr1:15898167
|
T | A | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-11154T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898167 | ||||||
chr1:15898173
|
T | TTG | 19 | a0001c0001t0001g0079a0001c0001t0001g0106a0001c0001t0001g0196others(16): Show | 19 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.882-11112_882-1111 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | |||||
chr1:15898173
|
T | TTGTG | 20 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(17): Show | 20 | HG00639.hp2 HG01175.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.882-11114_882-1111 others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | |||||
chr1:15898173
|
T | TTGTGTG | 16 | a0001c0001t0001g0067a0001c0001t0001g0073a0001c0001t0001g0108others(13): Show | 16 | HG01106.hp1 HG01106.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.882-11116_882-1111 others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | |||||
chr1:15898173
|
T | TTGTGTGT others(1): Show |
7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG01256.hp1 HG01261.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.882-11118_882-1111 others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | |||||
chr1:15898173
|
TTG | T | 62 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.882-11112_882-1111 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | |||||
chr1:15898173
|
TTGTG | T | 9 | a0001c0001t0001g0098a0001c0001t0001g0289a0001c0001t0001g0290others(6): Show | 9 | HG01074.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.882-11114_882-1111 others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | |||||
chr1:15898173
|
TTGTGTG | T | 13 | a0001c0001t0001g0023a0002c0002t0001g0004a0002c0002t0001g0213others(10): Show | 13 | HG00280.hp1 HG00621.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.882-11116_882-1111 others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | |||||
chr1:15898173
|
TTGTGTGT others(1): Show |
T | 3 | a0002c0002t0001g0190a0002c0002t0001g0278a0004c0009t0001g0114 | 3 | HG02970.hp1 NA18966.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.882-11118_882-1111 others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | |||||
chr1:15898173
|
TTGTGTGT others(3): Show |
T | 10 | a0001c0027t0001g0076a0003c0003t0001g0123a0003c0003t0001g0126others(7): Show | 10 | HG01123.hp2 HG01192.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-11120_882-1111 others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | |||||
chr1:15898173
|
TTGTGTGT others(5): Show |
T | 62 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.882-11122_882-1111 others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | |||||
chr1:15898233
|
C | T | 1 | a0002c0002t0001g0274 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.882-11088C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898233 | ||||||
chr1:15898382
|
G | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.882-10939G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898382 | ||||||
chr1:15898503
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.882-10818T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898503 | ||||||
chr1:15898558
|
C | CT | 52 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.882-10748dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898558 | |||||
chr1:15898681
|
T | G | 1 | a0003c0003t0001g0152 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.882-10640T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898681 | ||||||
chr1:15898682
|
C | G | 1 | a0003c0003t0001g0156 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.882-10639C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898682 | ||||||
chr1:15899003
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.882-10318A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899003 | ||||||
chr1:15899022
|
G | A | 2 | a0002c0002t0001g0241a0002c0002t0001g0246 | 2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.882-10299G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899022 | ||||||
chr1:15899069
|
G | T | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882-10252G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899069 | ||||||
chr1:15899174
|
T | G | 4 | a0007c0010t0001g0218a0007c0010t0001g0219a0007c0010t0001g0220others(1): Show | 4 | NA18954.hp1 NA19064.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-10147T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899174 | ||||||
chr1:15899233
|
C | T | 25 | a0003c0003t0001g0122a0003c0003t0001g0134a0003c0003t0001g0135others(22): Show | 25 | HG00438.hp1 HG00544.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.882-10088C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899233 | ||||||
chr1:15899342
|
T | A | 3 | a0006c0012t0001g0103a0006c0012t0001g0104a0006c0012t0001g0105 | 3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.882-9979T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899342 | ||||||
chr1:15899394
|
G | C | 1 | a0003c0003t0007g0162 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.882-9927G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899394 | ||||||
chr1:15899458
|
G | A | 1 | a0002c0002t0001g0225 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.882-9863G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899458 | ||||||
chr1:15899477
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.882-9844G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899477 | ||||||
chr1:15899537
|
G | GT | 105 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0037others(102): Show | 105 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.882-9758dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15899537 | |||||
chr1:15899537
|
G | GTT | 30 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 30 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.882-9759_882-9758d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15899537 | |||||
chr1:15899537
|
GT | G | 21 | a0001c0001t0001g0045a0001c0001t0001g0098a0001c0001t0006g0097others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.882-9758delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15899537 | |||||
chr1:15899668
|
A | G | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.882-9653A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899668 | ||||||
chr1:15900139
|
A | C | 197 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.882-9182A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15900139 | ||||||
chr1:15900378
|
G | A | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-8943G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15900378 | ||||||
chr1:15900405
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882-8916G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15900405 | ||||||
chr1:15900713
|
GAA | G | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-8606_882-8605d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15900713 | |||||
chr1:15900855
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882-8466G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15900855 | ||||||
chr1:15900949
|
T | C | 1 | a0003c0003t0001g0150 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.882-8372T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15900949 | ||||||
chr1:15901024
|
T | C | 1 | a0014c0034t0001g0265 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.882-8297T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901024 | ||||||
chr1:15901028
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.882-8293T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901028 | ||||||
chr1:15901125
|
G | A | 2 | a0002c0002t0001g0241a0002c0002t0001g0246 | 2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.882-8196G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901125 | ||||||
chr1:15901294
|
G | A | 1 | a0003c0003t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.882-8027G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901294 | ||||||
chr1:15901327
|
T | A | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-7994T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901327 | ||||||
chr1:15901348
|
T | TA | 8 | a0005c0005t0001g0204a0005c0005t0001g0208a0005c0005t0001g0209others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-7963dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901348 | |||||
chr1:15901415
|
T | C | 1 | a0003c0003t0001g0138 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.882-7906T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901415 | ||||||
chr1:15901512
|
T | C | 87 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(84): Show | 87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.882-7809T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901512 | ||||||
chr1:15901591
|
A | G | 1 | a0023c0035t0001g0176 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.882-7730A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901591 | ||||||
chr1:15901649
|
C | CA | 28 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0047others(25): Show | 28 | HG00673.hp1 HG01123.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.882-7652dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901649 | |||||
chr1:15901649
|
CA | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0205a0001c0001t0001g0206others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.882-7652delA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901649 | |||||
chr1:15901665
|
A | AC | 4 | a0003c0003t0001g0145a0003c0003t0001g0147a0003c0003t0001g0153others(1): Show | 4 | HG01934.hp2 HG02015.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-7656_882-7655i others(3): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901665 | ||||||
chr1:15901665
|
A | C | 82 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(79): Show | 82 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.882-7656A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901665 | ||||||
chr1:15901703
|
C | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-7618C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901703 | ||||||
chr1:15901839
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-7482C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901839 | ||||||
chr1:15901861
|
A | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0297 | 2 | HG00639.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.882-7460A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901861 | ||||||
chr1:15901867
|
T | C | 3 | a0001c0004t0001g0089a0001c0004t0001g0090a0001c0004t0001g0091 | 3 | HG02486.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.882-7454T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901867 | ||||||
chr1:15901914
|
T | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.882-7407T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901914 | ||||||
chr1:15901928
|
G | GT | 10 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(7): Show | 10 | HG02258.hp2 HG02273.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-7373dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901928 | |||||
chr1:15901928
|
GT | G | 126 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.882-7373delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901928 | |||||
chr1:15901928
|
GTT | G | 68 | a0001c0023t0003g0006a0003c0003t0001g0109a0003c0003t0001g0121others(65): Show | 68 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.882-7374_882-7373d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901928 | |||||
chr1:15901928
|
GTTT | G | 10 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-7375_882-7373d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901928 | |||||
chr1:15901948
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.882-7373T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901948 | ||||||
chr1:15902031
|
C | T | 1 | a0001c0026t0001g0096 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.882-7290C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902031 | ||||||
chr1:15902055
|
A | G | 19 | a0001c0004t0001g0064a0001c0004t0001g0081a0001c0004t0001g0083others(16): Show | 19 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.882-7266A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902055 | ||||||
chr1:15902244
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.882-7077C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902244 | ||||||
chr1:15902285
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.882-7036T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902285 | ||||||
chr1:15902356
|
C | T | 1 | a0002c0002t0001g0269 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.882-6965C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902356 | ||||||
chr1:15902357
|
A | C | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-6964A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902357 | ||||||
chr1:15902418
|
T | C | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-6903T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902418 | ||||||
chr1:15902464
|
T | TA | 87 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(84): Show | 87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.882-6849dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15902464 | |||||
chr1:15902476
|
G | C | 1 | a0002c0002t0001g0259 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.882-6845G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902476 | ||||||
chr1:15902589
|
C | T | 56 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(53): Show | 56 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.882-6732C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902589 | ||||||
chr1:15902639
|
G | A | 1 | a0002c0002t0004g0244 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.882-6682G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902639 | ||||||
chr1:15902734
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.882-6587T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902734 | ||||||
chr1:15902879
|
C | A | 2 | a0002c0002t0001g0190a0002c0002t0001g0278 | 2 | NA18966.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.882-6442C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902879 | ||||||
chr1:15903102
|
A | T | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-6219A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15903102 | ||||||
chr1:15903239
|
G | A | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882-6082G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15903239 | ||||||
chr1:15903567
|
G | A | 86 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(83): Show | 86 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.882-5754G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15903567 | ||||||
chr1:15903597
|
A | T | 1 | a0001c0004t0001g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.882-5724A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15903597 | ||||||
chr1:15903897
|
A | G | 2 | a0001c0029t0001g0094a0019c0030t0001g0080 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.882-5424A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15903897 | ||||||
chr1:15904162
|
T | C | 87 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(84): Show | 87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.882-5159T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904162 | ||||||
chr1:15904215
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882-5106T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904215 | ||||||
chr1:15904245
|
A | G | 8 | a0005c0005t0001g0204a0005c0005t0001g0208a0005c0005t0001g0209others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-5076A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904245 | ||||||
chr1:15904452
|
C | CA | 16 | a0001c0001t0001g0203a0002c0002t0001g0004a0002c0002t0001g0005others(13): Show | 16 | HG00621.hp1 HG01123.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.882-4844dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAA | 41 | a0001c0001t0001g0078a0002c0002t0001g0231a0002c0002t0001g0242others(38): Show | 41 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.882-4845_882-4844d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAA | 22 | a0001c0001t0001g0079a0003c0003t0001g0109a0003c0003t0001g0121others(19): Show | 22 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.882-4846_882-4844d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAA | 14 | a0001c0001t0001g0045a0003c0003t0001g0123a0003c0003t0001g0126others(11): Show | 14 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.882-4847_882-4844d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAA | 6 | a0003c0003t0001g0130a0003c0003t0001g0131a0003c0003t0001g0165others(3): Show | 6 | HG01123.hp2 HG01192.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.882-4848_882-4844d others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAA | 10 | a0001c0001t0001g0202a0001c0017t0001g0060a0003c0003t0001g0141others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.882-4849_882-4844d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA | 10 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0198others(7): Show | 10 | HG02109.hp1 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.882-4850_882-4844d others(9): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0194others(5): Show | 8 | HG01106.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-4851_882-4844d others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.882-4853_882-4844d others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0051 | 2 | HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.882-4855_882-4844d others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0290others(5): Show | 8 | HG00323.hp2 HG01069.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-4856_882-4844d others(15): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(7): Show |
12 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(9): Show | 12 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.882-4857_882-4844d others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(8): Show |
7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0029others(4): Show | 7 | HG00099.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.882-4858_882-4844d others(17): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0031others(1): Show | 4 | HG01175.hp1 HG01243.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-4859_882-4844d others(18): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0009a0020c0031t0001g0007 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.882-4860_882-4844d others(19): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058 | 3 | HG00280.hp1 HG01168.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.882-4863_882-4844d others(22): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0056others(1): Show | 4 | HG00544.hp1 HG00621.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-4865_882-4844d others(24): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0061a0001c0015t0001g0046a0001c0015t0001g0062 | 3 | HG02132.hp1 HG03654.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.882-4866_882-4844d others(25): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.882-4868_882-4844d others(27): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0057 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.882-4844_882-4843i others(31): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.882-4844_882-4843i others(32): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.882-4844_882-4843i others(38): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
CAA | C | 8 | a0001c0001t0001g0289a0001c0004t0001g0086a0001c0007t0001g0293others(5): Show | 8 | HG02622.hp2 HG03130.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-4845_882-4844d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
CAAAA | C | 15 | a0001c0004t0001g0064a0001c0004t0001g0081a0001c0004t0001g0083others(12): Show | 15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.882-4847_882-4844d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904452
|
CAAAAAAA | C | 33 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(30): Show | 33 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.882-4850_882-4844d others(9): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | |||||
chr1:15904478
|
G | A | 69 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(66): Show | 69 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.882-4843G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904478 | ||||||
chr1:15904479
|
T | A | 69 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(66): Show | 69 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.882-4842T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904479 | ||||||
chr1:15904535
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.882-4786C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904535 | ||||||
chr1:15904648
|
A | AT | 23 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(20): Show | 23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.882-4657dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904648 | |||||
chr1:15904648
|
AT | A | 90 | a0001c0001t0001g0022a0001c0001t0001g0074a0001c0007t0001g0293others(87): Show | 90 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.882-4657delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904648 | |||||
chr1:15904712
|
C | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-4609C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904712 | ||||||
chr1:15904717
|
T | C | 24 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(21): Show | 24 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.882-4604T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904717 | ||||||
chr1:15905012
|
C | T | 1 | a0002c0002t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.882-4309C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905012 | ||||||
chr1:15905076
|
T | C | 1 | a0004c0009t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.882-4245T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905076 | ||||||
chr1:15905251
|
T | C | 221 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.882-4070T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905251 | ||||||
chr1:15905314
|
C | G | 31 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(28): Show | 31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.882-4007C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905314 | ||||||
chr1:15905324
|
C | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-3997C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905324 | ||||||
chr1:15905338
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.882-3983C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905338 | ||||||
chr1:15905527
|
T | A | 1 | a0002c0002t0001g0216 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.882-3794T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905527 | ||||||
chr1:15905844
|
A | G | 1 | a0001c0001t0001g0013 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.882-3477A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905844 | ||||||
chr1:15905913
|
C | T | 2 | a0003c0003t0001g0166a0003c0003t0001g0174 | 2 | HG02071.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.882-3408C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905913 | ||||||
chr1:15905956
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-3365G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905956 | ||||||
chr1:15906139
|
C | T | 5 | a0003c0003t0001g0168a0003c0003t0001g0169a0003c0003t0001g0170others(2): Show | 5 | HG01168.hp2 HG01255.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.882-3182C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906139 | ||||||
chr1:15906196
|
C | T | 1 | a0002c0002t0001g0239 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.882-3125C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906196 | ||||||
chr1:15906345
|
T | G | 2 | a0002c0002t0001g0238a0002c0002t0001g0250 | 2 | NA18944.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.882-2976T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906345 | ||||||
chr1:15906453
|
C | CT | 24 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(21): Show | 24 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.882-2843dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906453 | |||||
chr1:15906453
|
CT | C | 54 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0031others(51): Show | 54 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.882-2843delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906453 | |||||
chr1:15906453
|
CTT | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0023others(6): Show | 9 | HG00280.hp1 HG01069.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.882-2844_882-2843d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906453 | |||||
chr1:15906453
|
CTTT | C | 42 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.882-2845_882-2843d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906453 | |||||
chr1:15906453
|
CTTTTTTT others(7): Show |
C | 74 | a0001c0001t0001g0037a0001c0001t0001g0038a0002c0002t0001g0216others(71): Show | 74 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.882-2856_882-2843d others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906453 | |||||
chr1:15906485
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.882-2836G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906485 | ||||||
chr1:15906557
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-2764C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906557 | ||||||
chr1:15906605
|
C | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-2716C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906605 | ||||||
chr1:15906631
|
T | C | 1 | a0002c0002t0004g0244 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.882-2690T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906631 | ||||||
chr1:15906773
|
C | CT | 29 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0037others(26): Show | 29 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.882-2527dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906773 | |||||
chr1:15906773
|
C | CTT | 16 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0077others(13): Show | 16 | HG01070.hp1 HG01071.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.882-2528_882-2527d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906773 | |||||
chr1:15906773
|
CT | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0048a0001c0001t0001g0061others(112): Show | 115 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.882-2527delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906773 | |||||
chr1:15906876
|
G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-2445G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906876 | ||||||
chr1:15907384
|
G | A | 1 | a0002c0002t0001g0225 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.882-1937G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15907384 | ||||||
chr1:15907645
|
C | G | 1 | a0010c0016t0001g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.882-1676C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15907645 | ||||||
chr1:15908111
|
C | T | 1 | a0004c0009t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.882-1210C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908111 | ||||||
chr1:15908170
|
G | GCTA | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-1135_882-1133d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15908170 | |||||
chr1:15908297
|
C | T | 6 | a0002c0002t0001g0235a0002c0002t0001g0257a0002c0002t0001g0258others(3): Show | 6 | NA18971.hp2 NA19005.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.882-1024C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908297 | ||||||
chr1:15908427
|
C | CT | 25 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(22): Show | 25 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.882-883dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15908427 | |||||
chr1:15908523
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.882-798C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908523 | ||||||
chr1:15908595
|
A | G | 2 | a0001c0014t0001g0019a0001c0014t0001g0034 | 2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.882-726A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908595 | ||||||
chr1:15908623
|
A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.882-698A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908623 | ||||||
chr1:15908660
|
C | T | 2 | a0011c0013t0002g0054a0011c0013t0002g0055 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.882-661C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908660 | ||||||
chr1:15908885
|
A | C | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-436A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908885 | ||||||
chr1:15908908
|
C | T | 2 | a0002c0002t0001g0221a0002c0002t0001g0292 | 2 | HG02071.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.882-413C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908908 | ||||||
chr1:15908996
|
C | T | 2 | a0003c0003t0001g0160a0003c0003t0001g0161 | 2 | NA18968.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.882-325C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908996 | ||||||
chr1:15909229
|
T | G | 1 | a0021c0032t0001g0087 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.882-92T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15909229 | ||||||
chr1:15909500
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1042+19G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15909500 | ||||||
chr1:15909532
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+51G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15909532 | ||||||
chr1:15909605
|
C | T | 1 | a0002c0002t0001g0274 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1042+124C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15909605 | ||||||
chr1:15909985
|
G | A | 1 | a0003c0003t0001g0303 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1042+504G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15909985 | ||||||
chr1:15910055
|
C | T | 1 | a0003c0003t0001g0160 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1042+574C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910055 | ||||||
chr1:15910124
|
T | TA | 41 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0016others(38): Show | 41 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1042+670dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 15910124 | |||||
chr1:15910124
|
TA | T | 91 | a0001c0001t0001g0022a0001c0001t0001g0078a0001c0001t0001g0191others(88): Show | 91 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1042+670delA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 15910124 | |||||
chr1:15910124
|
TAA | T | 9 | a0001c0004t0001g0091a0004c0006t0001g0111a0004c0006t0001g0112others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1042+669_1042+670d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 15910124 | |||||
chr1:15910124
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1042+658_1042+670d others(15): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 15910124 | |||||
chr1:15910125
|
A | T | 2 | a0001c0014t0001g0019a0001c0014t0001g0034 | 2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1042+644A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910125 | ||||||
chr1:15910199
|
G | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1042+718G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910199 | ||||||
chr1:15910438
|
C | T | 1 | a0001c0004t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1043-663C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910438 | ||||||
chr1:15910519
|
A | G | 1 | a0015c0021t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1043-582A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910519 | ||||||
chr1:15910627
|
G | GT | 27 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(24): Show | 27 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1043-463dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 15910627 | |||||
chr1:15910816
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1043-285C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910816 | ||||||
chr1:15910817
|
G | A | 1 | a0003c0003t0001g0167 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1043-284G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910817 | ||||||
chr1:15911082
|
G | T | 24 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(21): Show | 24 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1043-19G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15911082 | ||||||
chr1:15911312
|
A | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+11A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15911312 | ||||||
chr1:15911521
|
A | G | 1 | a0002c0002t0001g0225 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1243+220A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15911521 | ||||||
chr1:15911522
|
A | T | 1 | a0002c0002t0001g0225 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1243+221A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15911522 | ||||||
chr1:15912048
|
A | G | 2 | a0001c0029t0001g0094a0019c0030t0001g0080 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1243+747A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912048 | ||||||
chr1:15912204
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1243+903G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912204 | ||||||
chr1:15912516
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1243+1215A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912516 | ||||||
chr1:15912717
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1243+1416G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912717 | ||||||
chr1:15912790
|
C | T | 1 | a0003c0003t0001g0135 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1243+1489C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912790 | ||||||
chr1:15912820
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0005g0001 | 3 | HG03041.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1243+1519T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912820 | ||||||
chr1:15912879
|
A | G | 2 | a0002c0002t0001g0280a0002c0002t0001g0283 | 2 | NA18953.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1243+1578A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912879 | ||||||
chr1:15912907
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1243+1606C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912907 | ||||||
chr1:15912945
|
G | C | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1243+1644G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912945 | ||||||
chr1:15913153
|
A | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0053 | 2 | HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1243+1852A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15913153 | ||||||
chr1:15913281
|
A | G | 2 | a0003c0003t0001g0144a0003c0003t0001g0145 | 2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1243+1980A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15913281 | ||||||
chr1:15913377
|
C | T | 2 | a0004c0006t0001g0112a0004c0006t0001g0113 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1243+2076C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15913377 | ||||||
chr1:15913435
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+2134C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15913435 | ||||||
chr1:15913715
|
C | G | 1 | a0001c0001t0001g0290 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1244-2413C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15913715 | ||||||
chr1:15914171
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1244-1957G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914171 | ||||||
chr1:15914420
|
A | G | 1 | a0022c0020t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1244-1708A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914420 | ||||||
chr1:15914454
|
C | T | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.1244-1674C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914454 | ||||||
chr1:15914548
|
C | T | 5 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0192others(2): Show | 5 | HG01106.hp2 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1244-1580C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914548 | ||||||
chr1:15914622
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1244-1506A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914622 | ||||||
chr1:15914639
|
A | G | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1244-1489A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914639 | ||||||
chr1:15914775
|
G | A | 1 | a0004c0009t0001g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1244-1353G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914775 | ||||||
chr1:15914959
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1244-1169G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914959 | ||||||
chr1:15915013
|
T | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1244-1115T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915013 | ||||||
chr1:15915067
|
C | T | 1 | a0002c0002t0001g0004 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1244-1061C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915067 | ||||||
chr1:15915086
|
A | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1244-1042A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915086 | ||||||
chr1:15915105
|
T | C | 1 | a0002c0002t0001g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1244-1023T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915105 | ||||||
chr1:15915325
|
G | A | 1 | a0003c0003t0001g0146 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1244-803G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915325 | ||||||
chr1:15915327
|
G | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(21): Show | 24 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1244-801G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915327 | ||||||
chr1:15915335
|
A | G | 31 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(28): Show | 31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1244-793A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915335 | ||||||
chr1:15915419
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1244-709G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915419 | ||||||
chr1:15915420
|
T | G | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1244-708T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915420 | ||||||
chr1:15915489
|
A | C | 31 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(28): Show | 31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1244-639A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915489 | ||||||
chr1:15915532
|
T | G | 1 | a0009c0011t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1244-596T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915532 | ||||||
chr1:15915680
|
G | A | 1 | a0003c0003t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1244-448G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915680 | ||||||
chr1:15915683
|
C | T | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1244-445C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915683 | ||||||
chr1:15915906
|
AT | A | 72 | a0002c0002t0001g0270a0003c0003t0001g0109a0003c0003t0001g0121others(69): Show | 72 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1244-213delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr1 | 15915906 | |||||
chr1:15916125
|
C | A | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
splice_region_variant&intron_variant | LOW | c.1244-3C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15916125 | ||||||
chr1:15916510
|
CT | C | 106 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1395+249delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 15916510 | |||||
chr1:15916599
|
C | T | 1 | a0001c0004t0001g0275 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1395+320C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15916599 | ||||||
chr1:15916755
|
T | C | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1395+476T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15916755 | ||||||
chr1:15916841
|
A | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1395+562A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15916841 | ||||||
chr1:15916929
|
C | A | 87 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(84): Show | 87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1395+650C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15916929 | ||||||
chr1:15916987
|
C | T | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1395+708C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15916987 | ||||||
chr1:15917068
|
C | T | 72 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(69): Show | 72 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1395+789C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917068 | ||||||
chr1:15917076
|
C | T | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1395+797C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917076 | ||||||
chr1:15917103
|
G | A | 86 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(83): Show | 86 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1395+824G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917103 | ||||||
chr1:15917452
|
C | T | 1 | a0002c0002t0001g0263 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1395+1173C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917452 | ||||||
chr1:15917530
|
C | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1395+1251C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917530 | ||||||
chr1:15917612
|
A | G | 3 | a0005c0005t0001g0208a0005c0005t0001g0209a0005c0005t0001g0288 | 3 | HG01069.hp2 HG01071.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1396-1314A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917612 | ||||||
chr1:15917840
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1396-1086A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917840 | ||||||
chr1:15918049
|
C | CT | 8 | a0002c0002t0001g0223a0002c0002t0001g0235a0002c0002t0001g0257others(5): Show | 8 | NA18971.hp2 NA18980.hp2 NA19005.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396-876dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 15918049 | |||||
chr1:15918101
|
T | A | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1396-825T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918101 | ||||||
chr1:15918319
|
A | G | 1 | a0001c0004t0001g0084 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1396-607A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918319 | ||||||
chr1:15918438
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1396-488C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918438 | ||||||
chr1:15918461
|
C | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1396-465C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918461 | ||||||
chr1:15918465
|
C | T | 1 | a0002c0002t0001g0227 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1396-461C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918465 | ||||||
chr1:15918476
|
C | T | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1396-450C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918476 | ||||||
chr1:15918513
|
G | A | 1 | a0003c0003t0001g0160 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1396-413G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918513 | ||||||
chr1:15918578
|
A | T | 1 | a0005c0005t0001g0204 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1396-348A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918578 | ||||||
chr1:15918745
|
G | A | 2 | a0003c0003t0001g0183a0003c0003t0001g0184 | 2 | HG00423.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1396-181G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918745 | ||||||
chr1:15918867
|
G | A | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1396-59G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918867 | ||||||
chr1:15919115
|
GT | G | 27 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(24): Show | 27 | HG00639.hp2 HG00735.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1521+74delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 15919115 | |||||
chr1:15919523
|
C | T | 2 | a0002c0002t0001g0271a0002c0002t0001g0279 | 2 | HG01255.hp1 HG01261.hp1 |
splice_region_variant&intron_variant | LOW | c.1635+6C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15919523 | ||||||
chr1:15919649
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0005g0001 | 3 | HG03041.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1635+132A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15919649 | ||||||
chr1:15920051
|
CT | C | 76 | a0001c0001t0001g0301a0001c0007t0001g0293a0001c0007t0001g0294others(73): Show | 76 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1635+546delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 15920051 | |||||
chr1:15920063
|
T | A | 1 | a0017c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1635+546T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920063 | ||||||
chr1:15920064
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1635+547A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920064 | ||||||
chr1:15920173
|
G | A | 2 | a0001c0029t0001g0094a0019c0030t0001g0080 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1635+656G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920173 | ||||||
chr1:15920179
|
C | T | 15 | a0001c0004t0001g0064a0001c0004t0001g0081a0001c0004t0001g0083others(12): Show | 15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1635+662C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920179 | ||||||
chr1:15920347
|
G | C | 15 | a0001c0004t0001g0064a0001c0004t0001g0081a0001c0004t0001g0083others(12): Show | 15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1636-523G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920347 | ||||||
chr1:15920708
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0006g0097 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1636-162G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920708 | ||||||
chr1:15920825
|
C | G | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1636-45C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920825 | ||||||
chr1:15921029
|
A | G | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1749+46A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921029 | ||||||
chr1:15921099
|
G | T | 1 | a0002c0002t0001g0190 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1749+116G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921099 | ||||||
chr1:15921186
|
G | A | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1749+203G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921186 | ||||||
chr1:15921421
|
T | C | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1749+438T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921421 | ||||||
chr1:15921568
|
C | G | 8 | a0005c0005t0001g0204a0005c0005t0001g0208a0005c0005t0001g0209others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1749+585C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921568 | ||||||
chr1:15921737
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1750-512C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921737 | ||||||
chr1:15921973
|
T | G | 7 | a0005c0005t0001g0208a0005c0005t0001g0209a0005c0005t0001g0210others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1750-276T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921973 | ||||||
chr1:15922453
|
A | G | 1 | a0001c0004t0001g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1850+104A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15922453 | ||||||
chr1:15922621
|
C | G | 2 | a0002c0002t0001g0258a0002c0018t0001g0276 | 2 | NA19011.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1850+272C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15922621 | ||||||
chr1:15922630
|
C | CT | 34 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(31): Show | 34 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1850+291dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15922630 | |||||
chr1:15923435
|
A | G | 31 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(28): Show | 31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1850+1086A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923435 | ||||||
chr1:15923479
|
CTTGAGTT others(3): Show |
C | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1850+1131_1850+114 others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923479 | ||||||
chr1:15923673
|
C | CT | 15 | a0001c0004t0001g0092a0002c0002t0001g0005a0002c0002t0001g0261others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1850+1338dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15923673 | |||||
chr1:15923784
|
C | T | 3 | a0002c0002t0001g0249a0002c0002t0001g0255a0002c0002t0004g0244 | 3 | NA18978.hp1 NA18995.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1850+1435C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923784 | ||||||
chr1:15923893
|
C | T | 1 | a0022c0020t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1850+1544C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923893 | ||||||
chr1:15923963
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1850+1614C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923963 | ||||||
chr1:15923971
|
C | G | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1850+1622C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923971 | ||||||
chr1:15924011
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1850+1662C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924011 | ||||||
chr1:15924066
|
A | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1850+1717A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924066 | ||||||
chr1:15924171
|
A | G | 87 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(84): Show | 87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1850+1822A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924171 | ||||||
chr1:15924286
|
G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1850+1937G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924286 | ||||||
chr1:15924714
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1850+2365C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924714 | ||||||
chr1:15924860
|
C | T | 3 | a0008c0008t0001g0099a0008c0008t0001g0100a0008c0008t0001g0101 | 3 | HG01167.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1850+2511C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924860 | ||||||
chr1:15924868
|
C | T | 1 | a0002c0002t0001g0190 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1850+2519C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924868 | ||||||
chr1:15925076
|
A | G | 59 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(56): Show | 59 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1850+2727A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925076 | ||||||
chr1:15925168
|
T | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1850+2819T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925168 | ||||||
chr1:15925197
|
G | A | 1 | a0003c0003t0001g0152 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1850+2848G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925197 | ||||||
chr1:15925252
|
C | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1851-2839C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925252 | ||||||
chr1:15925264
|
C | T | 1 | a0003c0003t0001g0151 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1851-2827C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925264 | ||||||
chr1:15925312
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1851-2779T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925312 | ||||||
chr1:15925405
|
C | T | 22 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(19): Show | 22 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1851-2686C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925405 | ||||||
chr1:15925557
|
CT | C | 25 | a0003c0003t0001g0122a0003c0003t0001g0134a0003c0003t0001g0135others(22): Show | 25 | HG00438.hp1 HG00544.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.1851-2527delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15925557 | |||||
chr1:15925594
|
A | ATT | 18 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(15): Show | 18 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.1851-2483_1851-248 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15925594 | |||||
chr1:15925608
|
T | C | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-2483T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925608 | ||||||
chr1:15926038
|
A | G | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1851-2053A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926038 | ||||||
chr1:15926175
|
C | A | 86 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(83): Show | 86 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1851-1916C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926175 | ||||||
chr1:15926372
|
C | T | 1 | a0003c0003t0001g0184 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1851-1719C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926372 | ||||||
chr1:15926384
|
T | C | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1851-1707T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926384 | ||||||
chr1:15926384
|
T | TAC | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1851-1679_1851-167 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926384 | |||||
chr1:15926384
|
T | TACAC | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011 | 3 | HG00735.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1851-1681_1851-167 others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926384 | |||||
chr1:15926384
|
TAC | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0074others(14): Show | 17 | HG01106.hp2 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1851-1679_1851-167 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926384 | |||||
chr1:15926384
|
TACACACA others(5): Show |
T | 1 | a0001c0015t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1851-1689_1851-167 others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926384 | |||||
chr1:15926412
|
C | T | 2 | a0001c0004t0001g0083a0001c0038t0001g0093 | 2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1851-1679C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926412 | ||||||
chr1:15926501
|
T | C | 71 | a0003c0003t0001g0109a0003c0003t0001g0121a0003c0003t0001g0122others(68): Show | 71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1851-1590T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926501 | ||||||
chr1:15926606
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1851-1485C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926606 | ||||||
chr1:15926617
|
G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1851-1474G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926617 | ||||||
chr1:15926694
|
C | CT | 25 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(22): Show | 25 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1851-1381dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926694 | |||||
chr1:15926694
|
CT | C | 69 | a0001c0023t0003g0006a0003c0003t0001g0109a0003c0003t0001g0122others(66): Show | 69 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1851-1381delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926694 | |||||
chr1:15926837
|
C | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1851-1254C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926837 | ||||||
chr1:15926922
|
A | G | 200 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1851-1169A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926922 | ||||||
chr1:15926969
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-1122G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926969 | ||||||
chr1:15927010
|
A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(2): Show | 5 | HG00099.hp2 HG01175.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1851-1081A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927010 | ||||||
chr1:15927087
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1851-1004A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927087 | ||||||
chr1:15927212
|
G | A | 2 | a0002c0002t0001g0249a0002c0002t0001g0255 | 2 | NA18978.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1851-879G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927212 | ||||||
chr1:15927224
|
A | G | 1 | a0002c0002t0001g0239 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1851-867A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927224 | ||||||
chr1:15927391
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1851-700T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927391 | ||||||
chr1:15927411
|
G | A | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-680G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927411 | ||||||
chr1:15927504
|
G | A | 8 | a0005c0005t0001g0204a0005c0005t0001g0208a0005c0005t0001g0209others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1851-587G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927504 | ||||||
chr1:15927523
|
T | A | 1 | a0002c0002t0001g0223 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1851-568T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927523 | ||||||
chr1:15927529
|
T | A | 1 | a0002c0002t0001g0223 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1851-562T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927529 | ||||||
chr1:15927532
|
G | A | 1 | a0002c0002t0001g0223 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1851-559G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927532 | ||||||
chr1:15927663
|
G | A | 4 | a0008c0008t0001g0099a0008c0008t0001g0100a0008c0008t0001g0101others(1): Show | 4 | HG01167.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-428G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927663 | ||||||
chr1:15928003
|
A | T | 2 | a0003c0003t0001g0109a0003c0003t0001g0165 | 2 | HG00558.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1851-88A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15928003 | ||||||
chr1:15928076
|
G | A | 24 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(21): Show | 24 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1851-15G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15928076 | ||||||
chr1:15936389
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.10026+123C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15936389 | ||||||
chr1:15936438
|
C | T | 11 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.10026+172C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15936438 | ||||||
chr1:15936642
|
C | CAAAAAAA others(1): Show |
89 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0014others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.10026+382_10026+38 others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 15936642 | |||||
chr1:15936642
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(4): Show | 7 | HG01175.hp1 HG01975.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.10026+381_10026+38 others(13): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 15936642 | |||||
chr1:15936642
|
C | CAAAAAAA others(3): Show |
9 | a0004c0006t0001g0002a0004c0006t0001g0111a0004c0006t0001g0112others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.10026+380_10026+38 others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 15936642 | |||||
chr1:15936642
|
C | CAAAAAAA others(4): Show |
1 | a0004c0006t0001g0116 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.10026+379_10026+38 others(15): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 15936642 | |||||
chr1:15936703
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.10026+437A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15936703 | ||||||
chr1:15936832
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.10027-331T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15936832 | ||||||
chr1:15936957
|
A | G | 200 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.10027-206A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15936957 | ||||||
chr1:15937107
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.10027-56A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15937107 | ||||||
chr1:15937652
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp2 | splice_region_variant&intron_variant | LOW | c.10509+7A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 12/14 | chr1 | 15937652 | ||||||
chr1:15937728
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.10509+83C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 12/14 | chr1 | 15937728 | ||||||
chr1:15937769
|
G | A | 74 | a0001c0004t0001g0089a0001c0004t0001g0090a0001c0004t0001g0091others(71): Show | 74 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.10510-43G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 12/14 | chr1 | 15937769 | ||||||
chr1:15938217
|
C | G | 1 | a0019c0030t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.10704+211C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | chr1 | 15938217 | ||||||
chr1:15938565
|
C | CT | 19 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0032others(16): Show | 19 | HG00741.hp2 HG01074.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.10705-134dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 15938565 | |||||
chr1:15938565
|
CT | C | 55 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.10705-134delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 15938565 | |||||
chr1:15938565
|
CTT | C | 58 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0029t0001g0094others(55): Show | 58 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.10705-135_10705-13 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 15938565 | |||||
chr1:15938584
|
T | C | 16 | a0003c0003t0001g0124a0003c0003t0001g0139a0003c0003t0001g0140others(13): Show | 16 | HG00423.hp1 HG00423.hp2 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.10705-134T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | chr1 | 15938584 | ||||||
chr1:15938589
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.10705-129C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | chr1 | 15938589 | ||||||
chr1:15938927
|
A | G | 200 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.10863+51A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 14/14 | chr1 | 15938927 | ||||||
chr1:15938965
|
A | C | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.10863+89A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 14/14 | chr1 | 15938965 | ||||||
chr1:15939030
|
C | T | 1 | a0003c0003t0001g0179 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.10863+154C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 14/14 | chr1 | 15939030 | ||||||
chr1:15939264
|
C | T | 4 | a0001c0007t0001g0293a0001c0007t0001g0294a0001c0007t0001g0295others(1): Show | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.10864-32C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 14/14 | chr1 | 15939264 |