geneid | 54891 |
---|---|
ensemblid | ENSG00000114933.16 |
hgncid | 25997 |
symbol | INO80D |
name | INO80 complex subunit D |
refseq_nuc | NM_017759.5 |
refseq_prot | NP_060229.3 |
ensembl_nuc | ENST00000403263.6 |
ensembl_prot | ENSP00000384198.1 |
mane_status | MANE Select |
chr | chr2 |
start | 205993721 |
end | 206086174 |
strand | - |
ver | v1.2 |
region | chr2:205993721-206086174 |
region5000 | chr2:205988721-206091174 |
regionname0 | INO80D_chr2_205993721_206086174 |
regionname5000 | INO80D_chr2_205988721_206091174 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1027 | 221 | 58 | 50 | 80 | 11 | 20 | 63 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002 | 0/0 | 1027 | 105 | 20 | 19 | 42 | 5 | 19 | 35 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0003 | 0/0 | 1027 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0004 | 0/0 | 1027 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0005 | 0/0 | 1027 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0006 | 0/0 | 1027 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0007 | 0/0 | 1027 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
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 | 3084 | 127 | 27 | 35 | 45 | 8 | 11 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0002 | 0/0 | 3084 | 97 | 16 | 19 | 41 | 5 | 16 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0003 | 1/0 | 3084 | 77 | 29 | 10 | 29 | 2 | 6 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0004 | 0/0 | 3084 | 10 | 0 | 4 | 3 | 1 | 2 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0005 | 0/0 | 3084 | 4 | 4 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0006 | 0/0 | 3084 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0007 | 0/0 | 3084 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0008 | 0/0 | 3084 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0009 | 0/0 | 3084 | 2 | 1 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0010 | 0/0 | 3084 | 2 | 0 | 0 | 0 | 0 | 2 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0011 | 0/0 | 3084 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0012 | 0/0 | 3084 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0013 | 0/0 | 3084 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0014 | 0/0 | 3084 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0015 | 0/0 | 3084 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0016 | 0/0 | 3084 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
c0017 | 0/0 | 3084 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
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 | 0/0 | 11045 | 85 | 12 | 18 | 37 | 4 | 14 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0002 | 1/0 | 11045 | 54 | 25 | 6 | 15 | 2 | 5 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0003 | 0/0 | 11043 | 44 | 2 | 9 | 22 | 5 | 6 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0004 | 0/0 | 11045 | 19 | 0 | 14 | 0 | 3 | 2 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0005 | 0/0 | 11043 | 14 | 0 | 1 | 13 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0006 | 0/0 | 11046 | 13 | 3 | 3 | 7 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0007 | 0/0 | 11045 | 9 | 0 | 6 | 1 | 1 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0008 | 0/0 | 11046 | 6 | 6 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0009 | 0/0 | 11044 | 6 | 6 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0010 | 0/0 | 11046 | 5 | 1 | 1 | 2 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0011 | 0/0 | 11046 | 5 | 3 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0012 | 0/0 | 11044 | 4 | 0 | 0 | 4 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0013 | 0/0 | 11045 | 4 | 4 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0014 | 0/0 | 11045 | 4 | 0 | 0 | 4 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0015 | 0/0 | 11045 | 3 | 0 | 3 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0016 | 0/0 | 11045 | 3 | 3 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0017 | 0/0 | 11045 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0018 | 0/0 | 11046 | 2 | 0 | 2 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0019 | 0/0 | 11045 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0020 | 0/0 | 11043 | 2 | 0 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0021 | 0/0 | 11043 | 2 | 0 | 2 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0022 | 0/0 | 11044 | 2 | 1 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0023 | 0/0 | 11045 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0024 | 0/0 | 11045 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0025 | 0/0 | 11044 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0026 | 0/0 | 11044 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0027 | 0/0 | 11044 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0028 | 0/0 | 11044 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0029 | 0/0 | 11044 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0030 | 0/0 | 11029 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0031 | 0/0 | 11042 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0032 | 0/0 | 11045 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0033 | 0/0 | 11045 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0034 | 0/0 | 11043 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0035 | 0/0 | 11045 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0036 | 0/0 | 11045 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0037 | 0/0 | 11045 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0038 | 0/0 | 11043 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0039 | 0/0 | 11045 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0040 | 0/0 | 11043 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0041 | 0/0 | 11044 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0042 | 0/0 | 11044 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0043 | 0/0 | 11044 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0044 | 0/0 | 11045 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0045 | 0/0 | 11045 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0046 | 0/0 | 11044 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0047 | 0/0 | 11045 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0048 | 0/0 | 11046 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0049 | 0/0 | 11045 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0050 | 0/0 | 11046 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0051 | 0/0 | 11045 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0052 | 0/0 | 11045 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0053 | 0/1 | 11043 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0054 | 0/0 | 11045 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0055 | 0/0 | 11045 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0056 | 0/0 | 11045 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0057 | 0/0 | 11045 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0058 | 0/0 | 11046 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0059 | 0/0 | 11045 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0060 | 0/0 | 11045 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0061 | 0/0 | 11056 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0062 | 0/0 | 11045 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0063 | 0/0 | 11046 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
t0064 | 0/0 | 11045 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
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 | 3084 | 127 | 27 | 35 | 45 | 8 | 11 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003 | 1/0 | 3084 | 77 | 29 | 10 | 29 | 2 | 6 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0004 | 0/0 | 3084 | 10 | 0 | 4 | 3 | 1 | 2 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0006 | 0/0 | 3084 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0008 | 0/0 | 3084 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0011 | 0/0 | 3084 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0013 | 0/0 | 3084 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002 | 0/0 | 3084 | 97 | 16 | 19 | 41 | 5 | 16 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0005 | 0/0 | 3084 | 4 | 4 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0010 | 0/0 | 3084 | 2 | 0 | 0 | 0 | 0 | 2 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0016 | 0/0 | 3084 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0017 | 0/0 | 3084 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0003c0007 | 0/0 | 3084 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0004c0009 | 0/0 | 3084 | 2 | 1 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0005c0015 | 0/0 | 3084 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0006c0014 | 0/0 | 3084 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0007c0012 | 0/0 | 3084 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 14128 | 3 | 2 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0003 | 0/0 | 14126 | 43 | 2 | 9 | 22 | 5 | 5 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0004 | 0/0 | 14128 | 19 | 0 | 14 | 0 | 3 | 2 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0005 | 0/0 | 14126 | 13 | 0 | 0 | 13 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0008 | 0/0 | 14129 | 6 | 6 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0009 | 0/0 | 14127 | 6 | 6 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0012 | 0/0 | 14127 | 4 | 0 | 0 | 4 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0013 | 0/0 | 14128 | 4 | 4 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0015 | 0/0 | 14128 | 3 | 0 | 3 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0016 | 0/0 | 14128 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0018 | 0/0 | 14129 | 2 | 0 | 2 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0020 | 0/0 | 14126 | 2 | 0 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0021 | 0/0 | 14126 | 2 | 0 | 2 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0022 | 0/0 | 14127 | 2 | 1 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0024 | 0/0 | 14128 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0025 | 0/0 | 14127 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0026 | 0/0 | 14127 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0027 | 0/0 | 14127 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0028 | 0/0 | 14127 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0029 | 0/0 | 14127 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0030 | 0/0 | 14112 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0031 | 0/0 | 14125 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0032 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0034 | 0/0 | 14126 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0038 | 0/0 | 14126 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0041 | 0/0 | 14127 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0042 | 0/0 | 14127 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0050 | 0/0 | 14129 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0053 | 0/1 | 14126 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0001t0064 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0002 | 1/0 | 14128 | 48 | 21 | 6 | 14 | 2 | 4 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0006 | 0/0 | 14129 | 12 | 2 | 3 | 7 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0007 | 0/0 | 14128 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0011 | 0/0 | 14129 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0014 | 0/0 | 14128 | 4 | 0 | 0 | 4 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0017 | 0/0 | 14128 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0023 | 0/0 | 14128 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0054 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0059 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0061 | 0/0 | 14139 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0062 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0003t0063 | 0/0 | 14129 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0004t0007 | 0/0 | 14128 | 7 | 0 | 4 | 1 | 1 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0004t0011 | 0/0 | 14129 | 2 | 0 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0004t0037 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0006t0001 | 0/0 | 14128 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0008t0019 | 0/0 | 14128 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0011t0043 | 0/0 | 14127 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0001c0013t0005 | 0/0 | 14126 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0001 | 0/0 | 14128 | 79 | 12 | 18 | 32 | 4 | 13 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0010 | 0/0 | 14129 | 5 | 1 | 1 | 2 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0033 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0035 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0039 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0044 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0046 | 0/0 | 14127 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0047 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0048 | 0/0 | 14129 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0049 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0051 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0056 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0057 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0058 | 0/0 | 14129 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0002t0060 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0005t0002 | 0/0 | 14128 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0005t0006 | 0/0 | 14129 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0005t0040 | 0/0 | 14126 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0010t0001 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0010t0055 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0016t0036 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0002c0017t0052 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0003c0007t0001 | 0/0 | 14128 | 2 | 0 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0003c0007t0045 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0004c0009t0007 | 0/0 | 14128 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0004c0009t0011 | 0/0 | 14129 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0005c0015t0016 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0006c0014t0003 | 0/0 | 14126 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
a0007c0012t0002 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | copy fasta | chr2 | 205988721 | 206091174 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0009g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0009g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0012g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0012g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0012g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0013g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0015g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0015g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0015g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0016g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0016g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0018g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0018g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0020g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0020g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0021g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0021g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0022g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0022g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0024g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0025g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0026g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0027g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0028g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0029g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0030g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0031g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0032g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0034g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0038g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0041g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0042g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0050g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0053g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0001t0064g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0006g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0007g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0011g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0014g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0014g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0014g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0014g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0017g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0017g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0017g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0023g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0023g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0054g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0059g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0061g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0062g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0003t0063g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0004t0007g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0004t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0004t0007g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0004t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0004t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0004t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0004t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0004t0011g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0004t0011g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0004t0037g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0006t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0006t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0006t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0008t0019g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0008t0019g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0011t0043g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0001c0013t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0010g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0010g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0010g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0010g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0010g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0033g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0035g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0039g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0044g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0046g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0047g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0048g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0049g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0051g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0056g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0057g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0058g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0002t0060g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0005t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0005t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0005t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0005t0040g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0010t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0010t0055g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0016t0036g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0002c0017t0052g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0003c0007t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0003c0007t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0003c0007t0045g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0004c0009t0007g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0004c0009t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0005c0015t0016g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0006c0014t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
a0007c0012t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0057 | g0174 | EUR | GBR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00099 | hp2 | a0001 | c0003 | t0002 | g0278 | EUR | GBR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0072 | EUR | GBR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0196 | EUR | GBR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0184 | EUR | FIN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0068 | EUR | FIN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0146 | EUR | FIN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0049 | EUR | FIN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0231 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00438 | hp1 | a0001 | c0003 | t0014 | g0319 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0235 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00621 | hp2 | a0001 | c0003 | t0006 | g0288 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00639 | hp2 | a0001 | c0004 | t0007 | g0216 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00642 | hp1 | a0001 | c0013 | t0005 | g0228 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00673 | hp1 | a0001 | c0003 | t0006 | g0296 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00735 | hp2 | a0001 | c0001 | t0015 | g0010 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00741 | hp1 | a0001 | c0001 | t0018 | g0008 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01070 | hp2 | a0001 | c0003 | t0002 | g0260 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01074 | hp2 | a0001 | c0001 | t0015 | g0006 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01099 | hp1 | a0001 | c0001 | t0018 | g0005 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01106 | hp1 | a0001 | c0001 | t0030 | g0062 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01106 | hp2 | a0001 | c0001 | t0015 | g0007 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01109 | hp2 | a0001 | c0001 | t0022 | g0032 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01168 | hp1 | a0001 | c0001 | t0021 | g0046 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01169 | hp1 | a0001 | c0001 | t0021 | g0053 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01175 | hp1 | a0001 | c0004 | t0007 | g0218 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01175 | hp2 | a0001 | c0003 | t0002 | g0297 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01243 | hp1 | a0001 | c0004 | t0007 | g0220 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01243 | hp2 | a0001 | c0003 | t0007 | g0281 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01255 | hp1 | a0001 | c0003 | t0002 | g0293 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01255 | hp2 | a0001 | c0001 | t0025 | g0029 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01256 | hp2 | a0001 | c0001 | t0027 | g0009 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01257 | hp2 | a0004 | c0009 | t0007 | g0217 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0103 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01361 | hp1 | a0001 | c0003 | t0002 | g0304 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0028 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0294 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0050 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0017 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0014 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0266 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01891 | hp1 | a0001 | c0003 | t0011 | g0264 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01891 | hp2 | a0004 | c0009 | t0011 | g0215 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01928 | hp2 | a0001 | c0003 | t0006 | g0255 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01943 | hp1 | a0001 | c0003 | t0002 | g0276 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01978 | hp1 | a0001 | c0001 | t0024 | g0013 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01981 | hp1 | a0001 | c0003 | t0006 | g0301 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0211 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02055 | hp2 | a0001 | c0003 | t0011 | g0317 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02071 | hp1 | a0001 | c0003 | t0002 | g0199 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02071 | hp2 | a0001 | c0001 | t0005 | g0236 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02132 | hp2 | a0001 | c0003 | t0002 | g0127 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02135 | hp1 | a0001 | c0004 | t0011 | g0214 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0223 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0170 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02148 | hp2 | a0002 | c0002 | t0010 | g0137 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | CDX | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | CDX | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02257 | hp1 | a0005 | c0015 | t0016 | g0324 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02257 | hp2 | a0001 | c0001 | t0013 | g0035 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02258 | hp1 | a0001 | c0003 | t0002 | g0270 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02258 | hp2 | a0002 | c0005 | t0002 | g0327 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02280 | hp1 | a0001 | c0003 | t0002 | g0286 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02293 | hp2 | a0001 | c0003 | t0006 | g0320 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02300 | hp1 | a0001 | c0003 | t0002 | g0273 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02451 | hp1 | a0001 | c0001 | t0050 | g0239 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02451 | hp2 | a0002 | c0002 | t0049 | g0145 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02615 | hp1 | a0001 | c0003 | t0002 | g0259 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02615 | hp2 | a0001 | c0001 | t0013 | g0030 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0242 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02630 | hp2 | a0001 | c0003 | t0002 | g0261 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02683 | hp2 | a0001 | c0011 | t0043 | g0292 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02698 | hp2 | a0002 | c0002 | t0047 | g0117 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02717 | hp2 | a0001 | c0003 | t0002 | g0269 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0155 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0198 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0175 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02809 | hp1 | a0001 | c0003 | t0002 | g0274 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02809 | hp2 | a0002 | c0002 | t0051 | g0152 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02886 | hp1 | a0001 | c0003 | t0062 | g0254 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02895 | hp2 | a0001 | c0001 | t0016 | g0323 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02896 | hp1 | a0001 | c0003 | t0002 | g0318 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02896 | hp2 | a0001 | c0001 | t0008 | g0241 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0240 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02897 | hp2 | a0001 | c0001 | t0016 | g0322 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02970 | hp2 | a0001 | c0001 | t0041 | g0213 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0209 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03098 | hp1 | a0002 | c0005 | t0006 | g0328 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03098 | hp2 | a0001 | c0003 | t0006 | g0313 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03130 | hp2 | a0001 | c0003 | t0002 | g0267 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03139 | hp1 | a0001 | c0008 | t0019 | g0206 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03195 | hp1 | a0001 | c0001 | t0013 | g0207 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0325 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0238 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03209 | hp2 | a0002 | c0002 | t0056 | g0177 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03225 | hp1 | a0001 | c0003 | t0002 | g0262 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03225 | hp2 | a0001 | c0001 | t0009 | g0210 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0061 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03239 | hp2 | a0002 | c0010 | t0055 | g0176 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03453 | hp1 | a0001 | c0003 | t0002 | g0277 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03453 | hp2 | a0001 | c0001 | t0042 | g0031 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03486 | hp1 | a0001 | c0003 | t0059 | g0275 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03486 | hp2 | a0001 | c0003 | t0002 | g0268 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0126 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03492 | hp2 | a0001 | c0003 | t0054 | g0305 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03516 | hp1 | a0002 | c0002 | t0010 | g0173 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03516 | hp2 | a0001 | c0008 | t0019 | g0205 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03540 | hp1 | a0001 | c0003 | t0002 | g0263 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03540 | hp2 | a0001 | c0001 | t0013 | g0036 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03579 | hp1 | a0001 | c0001 | t0022 | g0034 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03654 | hp1 | a0001 | c0003 | t0002 | g0302 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03654 | hp2 | a0002 | c0002 | t0035 | g0118 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0201 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03669 | hp2 | a0001 | c0003 | t0002 | g0249 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03704 | hp1 | a0001 | c0001 | t0029 | g0063 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03704 | hp2 | a0001 | c0003 | t0063 | g0330 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0125 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03710 | hp2 | a0001 | c0004 | t0007 | g0212 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0153 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0023 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0178 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0306 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG04184 | hp1 | a0001 | c0003 | t0002 | g0290 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0156 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG04199 | hp1 | a0002 | c0002 | t0010 | g0109 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG04199 | hp2 | a0001 | c0004 | t0037 | g0204 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0150 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG04204 | hp2 | a0001 | c0001 | t0034 | g0225 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG04228 | hp1 | a0001 | c0001 | t0064 | g0331 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG04228 | hp2 | a0002 | c0010 | t0001 | g0116 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | CHB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18612 | hp2 | a0001 | c0003 | t0002 | g0279 | EAS | CHB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0229 | EAS | CHB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18747 | hp2 | a0001 | c0003 | t0002 | g0257 | EAS | CHB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0265 | AFR | YRI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18906 | hp2 | a0001 | c0003 | t0002 | g0315 | AFR | YRI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18943 | hp2 | a0001 | c0004 | t0007 | g0221 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18944 | hp2 | a0001 | c0003 | t0017 | g0311 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18945 | hp2 | a0001 | c0003 | t0014 | g0248 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18947 | hp2 | a0002 | c0002 | t0033 | g0180 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18948 | hp2 | a0001 | c0003 | t0017 | g0309 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18950 | hp2 | a0001 | c0003 | t0002 | g0300 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18951 | hp2 | a0001 | c0006 | t0001 | g0110 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18954 | hp2 | a0001 | c0003 | t0006 | g0298 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18957 | hp1 | a0002 | c0002 | t0060 | g0165 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18957 | hp2 | a0001 | c0003 | t0002 | g0316 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18960 | hp2 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18961 | hp1 | a0002 | c0002 | t0010 | g0139 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18961 | hp2 | a0001 | c0003 | t0002 | g0247 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18963 | hp1 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18964 | hp1 | a0001 | c0003 | t0002 | g0308 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18966 | hp1 | a0002 | c0017 | t0052 | g0099 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18966 | hp2 | a0001 | c0003 | t0014 | g0251 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18967 | hp1 | a0001 | c0003 | t0006 | g0321 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18967 | hp2 | a0001 | c0001 | t0028 | g0052 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18968 | hp1 | a0002 | c0002 | t0039 | g0130 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18968 | hp2 | a0001 | c0003 | t0017 | g0307 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18970 | hp1 | a0001 | c0003 | t0006 | g0299 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18970 | hp2 | a0001 | c0001 | t0012 | g0080 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18971 | hp1 | a0001 | c0001 | t0012 | g0084 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18975 | hp2 | a0001 | c0003 | t0006 | g0291 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18977 | hp1 | a0001 | c0006 | t0001 | g0122 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18979 | hp2 | a0001 | c0003 | t0002 | g0160 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18980 | hp2 | a0001 | c0001 | t0012 | g0082 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18983 | hp2 | a0001 | c0003 | t0002 | g0250 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18984 | hp1 | a0002 | c0002 | t0044 | g0151 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0224 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18986 | hp2 | a0003 | c0007 | t0001 | g0181 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18988 | hp1 | a0001 | c0001 | t0020 | g0038 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18988 | hp2 | a0001 | c0001 | t0038 | g0287 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18989 | hp2 | a0002 | c0002 | t0046 | g0245 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA18990 | hp2 | a0001 | c0003 | t0002 | g0303 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19000 | hp1 | a0001 | c0003 | t0002 | g0285 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19001 | hp1 | a0001 | c0001 | t0026 | g0004 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19001 | hp2 | a0001 | c0006 | t0001 | g0188 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19002 | hp1 | a0002 | c0002 | t0010 | g0244 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19004 | hp2 | a0001 | c0003 | t0014 | g0253 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19005 | hp2 | a0002 | c0002 | t0058 | g0102 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19009 | hp1 | a0001 | c0003 | t0006 | g0295 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19011 | hp2 | a0001 | c0001 | t0012 | g0086 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19030 | hp1 | a0001 | c0003 | t0002 | g0284 | AFR | LWK | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19030 | hp2 | a0001 | c0003 | t0002 | g0283 | AFR | LWK | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19054 | hp1 | a0001 | c0001 | t0005 | g0237 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19055 | hp1 | a0001 | c0001 | t0020 | g0037 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19056 | hp1 | a0001 | c0003 | t0061 | g0256 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19057 | hp2 | a0001 | c0004 | t0011 | g0219 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19058 | hp1 | a0001 | c0003 | t0002 | g0310 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19058 | hp2 | a0003 | c0007 | t0001 | g0163 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19066 | hp2 | a0001 | c0001 | t0032 | g0045 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19070 | hp2 | a0002 | c0002 | t0048 | g0119 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19074 | hp1 | a0003 | c0007 | t0045 | g0159 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19077 | hp1 | a0007 | c0012 | t0002 | g0252 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19085 | hp2 | a0001 | c0003 | t0002 | g0171 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19090 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | YRI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | YRI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA20129 | hp1 | a0001 | c0003 | t0023 | g0272 | AFR | ASW | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA20129 | hp2 | a0002 | c0005 | t0002 | g0190 | AFR | ASW | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA20805 | hp1 | a0001 | c0004 | t0007 | g0202 | EUR | TSI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0135 | EUR | TSI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA20905 | hp1 | a0002 | c0016 | t0036 | g0112 | SAS | GIH | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA20905 | hp2 | a0006 | c0014 | t0003 | g0075 | SAS | GIH | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG01123 | hp2 | a0001 | c0004 | t0007 | g0203 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02109 | hp1 | a0002 | c0005 | t0040 | g0326 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02109 | hp2 | a0001 | c0003 | t0002 | g0280 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02486 | hp1 | a0001 | c0001 | t0009 | g0329 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02486 | hp2 | a0001 | c0003 | t0006 | g0312 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG02559 | hp2 | a0001 | c0003 | t0002 | g0289 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0243 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG03471 | hp2 | a0001 | c0003 | t0002 | g0314 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG06807 | hp1 | a0001 | c0003 | t0002 | g0271 | AFR | USA | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
HG06807 | hp2 | a0001 | c0003 | t0023 | g0258 | AFR | USA | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | USA | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
NA20300 | hp2 | a0001 | c0001 | t0031 | g0246 | AFR | USA | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0053 | g0226 | REF | REF | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0113 | REF | REF | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:206004381
|
G | C | 1 | a0006 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.3071C>G | p.Pro1024Arg | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3468/14128 | 3071/3084 | 1024/1027 | chr2 | 206004381 | ||
chr2:206009583
|
T | C | 1 | a0004 | 2 | HG01257.hp2 HG01891.hp2 |
missense_variant | MODERATE | c.1754A>G | p.His585Arg | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/11 | 2151/14128 | 1754/3084 | 585/1027 | chr2 | 206009583 | ||
chr2:206028250
|
G | A | 1 | a0005 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1159C>T | p.Arg387Cys | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/11 | 1556/14128 | 1159/3084 | 387/1027 | chr2 | 206028250 | ||
chr2:206028318
|
G | A | 2 | a0003a0007 | 4 | NA18986.hp2 NA19058.hp2 NA19074.hp1 others(1): Show |
missense_variant | MODERATE | c.1091C>T | p.Ala364Val | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/11 | 1488/14128 | 1091/3084 | 364/1027 | chr2 | 206028318 | ||
chr2:206046504
|
G | A | 2 | a0002a0003 | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
missense_variant&splice_region_variant | MODERATE | c.1073C>T | p.Ala358Val | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/11 | 1470/14128 | 1073/3084 | 358/1027 | chr2 | 206046504 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:206005046
|
C | T | 1 | a0002c0010 | 2 | HG03239.hp2 HG04228.hp2 |
synonymous_variant | LOW | c.2406G>A | p.Leu802Leu | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2803/14128 | 2406/3084 | 802/1027 | chr2 | 206005046 | ||
chr2:206005085
|
G | A | 1 | a0001c0008 | 2 | HG03139.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.2367C>T | p.Asp789Asp | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2764/14128 | 2367/3084 | 789/1027 | chr2 | 206005085 | ||
chr2:206005229
|
C | T | 1 | a0002c0016 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.2223G>A | p.Leu741Leu | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2620/14128 | 2223/3084 | 741/1027 | chr2 | 206005229 | ||
chr2:206009615
|
G | A | 7 | a0001c0006a0001c0011a0002c0002others(4): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
synonymous_variant | LOW | c.1722C>T | p.Pro574Pro | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/11 | 2119/14128 | 1722/3084 | 574/1027 | chr2 | 206009615 | ||
chr2:206009642
|
T | A | 1 | a0002c0017 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.1695A>T | p.Ala565Ala | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/11 | 2092/14128 | 1695/3084 | 565/1027 | chr2 | 206009642 | ||
chr2:206017716
|
A | G | 1 | a0001c0013 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.1506T>C | p.His502His | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/11 | 1903/14128 | 1506/3084 | 502/1027 | chr2 | 206017716 | ||
chr2:206017806
|
G | C | 2 | a0001c0004a0004c0009 | 12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
synonymous_variant | LOW | c.1416C>G | p.Leu472Leu | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/11 | 1813/14128 | 1416/3084 | 472/1027 | chr2 | 206017806 | ||
chr2:206056727
|
G | A | 14 | a0001c0001a0001c0004a0001c0006others(11): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
synonymous_variant | LOW | c.435C>T | p.Thr145Thr | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/11 | 832/14128 | 435/3084 | 145/1027 | chr2 | 206056727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:205994481
|
T | A | 1 | a0001c0008t0019 | 2 | HG03139.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9887A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9887 | chr2 | 205994481 | |||||
chr2:205994594
|
T | A | 1 | a0002c0002t0047 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9774A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9774 | chr2 | 205994594 | |||||
chr2:205994609
|
C | A | 1 | a0001c0001t0042 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9759G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9759 | chr2 | 205994609 | |||||
chr2:205994795
|
T | C | 1 | a0001c0003t0017 | 3 | NA18944.hp2 NA18948.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9573A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9573 | chr2 | 205994795 | |||||
chr2:205994859
|
G | A | 3 | a0001c0001t0016a0001c0008t0019a0005c0015t0016 | 5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9509C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9509 | chr2 | 205994859 | |||||
chr2:205994874
|
C | CA | 9 | a0001c0001t0041a0001c0001t0042a0001c0003t0006others(6): Show | 20 | HG00621.hp2 HG00673.hp1 HG01928.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*9493dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9493 | chr2 | 205994874 | |||||
chr2:205994874
|
CA | C | 24 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(21): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*9493delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9493 | chr2 | 205994874 | |||||
chr2:205994967
|
C | G | 1 | a0001c0001t0031 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9401G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9401 | chr2 | 205994967 | |||||
chr2:205994999
|
G | T | 2 | a0001c0001t0041a0001c0001t0042 | 2 | HG02970.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9369C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9369 | chr2 | 205994999 | |||||
chr2:205995126
|
C | G | 1 | a0001c0001t0020 | 2 | NA18988.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9242G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9242 | chr2 | 205995126 | |||||
chr2:205995942
|
G | A | 1 | a0001c0003t0054 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8426C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 8426 | chr2 | 205995942 | |||||
chr2:205996326
|
A | AT | 26 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(23): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*8041dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 8041 | chr2 | 205996326 | |||||
chr2:205996346
|
T | C | 1 | a0002c0002t0049 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8022A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 8022 | chr2 | 205996346 | |||||
chr2:205996512
|
C | T | 1 | a0003c0007t0045 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7856G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7856 | chr2 | 205996512 | |||||
chr2:205996915
|
T | TA | 16 | a0001c0001t0003a0001c0001t0008a0001c0001t0012others(13): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*7452dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7452 | chr2 | 205996915 | |||||
chr2:205996920
|
A | AC | 7 | a0001c0001t0004a0001c0001t0015a0001c0001t0018others(4): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*7447_*7448insG | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7447 | chr2 | 205996920 | |||||
chr2:205996974
|
G | A | 2 | a0001c0001t0041a0001c0001t0042 | 2 | HG02970.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7394C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7394 | chr2 | 205996974 | |||||
chr2:205997280
|
T | C | 1 | a0001c0003t0014 | 4 | HG00438.hp1 NA18945.hp2 NA18966.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7088A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7088 | chr2 | 205997280 | |||||
chr2:205997291
|
G | A | 23 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(20): Show | 98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*7077C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7077 | chr2 | 205997291 | |||||
chr2:205997458
|
A | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6910T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 6910 | chr2 | 205997458 | |||||
chr2:205997920
|
G | A | 1 | a0001c0001t0053 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6448C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 6448 | chr2 | 205997920 | |||||
chr2:205998166
|
T | C | 1 | a0002c0002t0051 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6202A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 6202 | chr2 | 205998166 | |||||
chr2:205998450
|
C | CA | 2 | a0002c0002t0010a0002c0002t0058 | 6 | HG02148.hp2 HG03516.hp1 HG04199.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5917dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5917 | chr2 | 205998450 | |||||
chr2:205998450
|
CA | C | 23 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(20): Show | 76 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*5917delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5917 | chr2 | 205998450 | |||||
chr2:205998450
|
CAA | C | 12 | a0001c0001t0003a0001c0001t0020a0001c0001t0021others(9): Show | 56 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*5916_*5917delTT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5916 | chr2 | 205998450 | |||||
chr2:205999150
|
C | T | 51 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(48): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*5218G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5218 | chr2 | 205999150 | |||||
chr2:205999178
|
AAAAAACA others(7): Show |
A | 1 | a0001c0001t0030 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5176_*5189delGTTT others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5176 | chr2 | 205999178 | |||||
chr2:205999254
|
G | C | 1 | a0002c0017t0052 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5114C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5114 | chr2 | 205999254 | |||||
chr2:205999262
|
G | A | 2 | a0001c0001t0013a0001c0001t0022 | 6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5106C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5106 | chr2 | 205999262 | |||||
chr2:205999557
|
CA | C | 21 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(18): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*4810delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 4810 | chr2 | 205999557 | |||||
chr2:205999595
|
G | C | 2 | a0001c0001t0016a0005c0015t0016 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4773C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 4773 | chr2 | 205999595 | |||||
chr2:206000040
|
C | T | 51 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(48): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*4328G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 4328 | chr2 | 206000040 | |||||
chr2:206000140
|
G | A | 10 | a0001c0001t0003a0001c0001t0012a0001c0001t0020others(7): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*4228C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 4228 | chr2 | 206000140 | |||||
chr2:206000305
|
C | T | 1 | a0002c0002t0039 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4063G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 4063 | chr2 | 206000305 | |||||
chr2:206000522
|
A | G | 7 | a0001c0001t0004a0001c0001t0015a0001c0001t0018others(4): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3846T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3846 | chr2 | 206000522 | |||||
chr2:206000573
|
C | G | 1 | a0001c0001t0038 | 1 | NA18988.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3795G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3795 | chr2 | 206000573 | |||||
chr2:206000638
|
G | T | 1 | a0001c0004t0037 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3730C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3730 | chr2 | 206000638 | |||||
chr2:206000739
|
A | G | 1 | a0002c0016t0036 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3629T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3629 | chr2 | 206000739 | |||||
chr2:206000886
|
T | A | 1 | a0002c0010t0055 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3482A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3482 | chr2 | 206000886 | |||||
chr2:206001023
|
T | C | 1 | a0002c0002t0056 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3345A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3345 | chr2 | 206001023 | |||||
chr2:206001234
|
T | C | 1 | a0002c0002t0057 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3134A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3134 | chr2 | 206001234 | |||||
chr2:206001378
|
G | A | 1 | a0002c0002t0058 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2990C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2990 | chr2 | 206001378 | |||||
chr2:206001476
|
T | C | 1 | a0001c0001t0031 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2892A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2892 | chr2 | 206001476 | |||||
chr2:206002056
|
C | T | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(15): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*2312G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2312 | chr2 | 206002056 | |||||
chr2:206002109
|
T | C | 1 | a0001c0003t0059 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2259A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2259 | chr2 | 206002109 | |||||
chr2:206002362
|
T | C | 1 | a0002c0002t0060 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2006A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2006 | chr2 | 206002362 | |||||
chr2:206002731
|
A | T | 1 | a0001c0003t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1637T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1637 | chr2 | 206002731 | |||||
chr2:206002734
|
C | CTATTTAT others(3): Show |
1 | a0001c0003t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1633_*1634insCTTA others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1633 | chr2 | 206002734 | |||||
chr2:206002735
|
A | G | 1 | a0001c0003t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1633T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1633 | chr2 | 206002735 | |||||
chr2:206002736
|
C | A | 1 | a0001c0003t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1632G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1632 | chr2 | 206002736 | |||||
chr2:206002997
|
C | T | 1 | a0002c0002t0035 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1371G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1371 | chr2 | 206002997 | |||||
chr2:206003038
|
A | G | 4 | a0001c0001t0004a0001c0001t0024a0001c0001t0025others(1): Show | 22 | HG00738.hp1 HG01123.hp1 HG01255.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1330T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1330 | chr2 | 206003038 | |||||
chr2:206003126
|
G | C | 1 | a0001c0003t0023 | 2 | HG06807.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1242C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1242 | chr2 | 206003126 | |||||
chr2:206003603
|
G | A | 1 | a0001c0001t0021 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*765C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 765 | chr2 | 206003603 | |||||
chr2:206003616
|
C | T | 1 | a0001c0001t0034 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 752 | chr2 | 206003616 | |||||
chr2:206003649
|
G | A | 1 | a0001c0001t0032 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*719C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 719 | chr2 | 206003649 | |||||
chr2:206003652
|
C | G | 1 | a0002c0002t0033 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 716 | chr2 | 206003652 | |||||
chr2:206003714
|
T | C | 1 | a0001c0003t0062 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*654A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 654 | chr2 | 206003714 | |||||
chr2:206003998
|
C | T | 21 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(18): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*370G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 370 | chr2 | 206003998 | |||||
chr2:206004367
|
C | T | 1 | a0001c0001t0024 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1 | chr2 | 206004367 | |||||
chr2:206085904
|
T | A | 1 | a0001c0003t0063 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-127A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/11 | 22888 | chr2 | 206085904 | |||||
chr2:206085911
|
C | CT | 8 | a0001c0001t0004a0001c0001t0015a0001c0001t0018others(5): Show | 29 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-135dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/11 | 22896 | chr2 | 206085911 | |||||
chr2:206085980
|
T | G | 1 | a0001c0001t0064 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-203A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/11 | 22964 | chr2 | 206085980 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:206005554
|
G | A | 1 | a0001c0003t0002g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1919-21C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005554 | ||||||
chr2:206005584
|
A | G | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1919-51T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005584 | ||||||
chr2:206005765
|
T | A | 96 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(93): Show | 98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1919-232A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005765 | ||||||
chr2:206005810
|
T | C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1919-277A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005810 | ||||||
chr2:206005857
|
G | A | 2 | a0001c0003t0002g0284a0002c0002t0001g0003 | 3 | HG02630.hp1 HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1919-324C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005857 | ||||||
chr2:206005883
|
C | G | 12 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212others(9): Show | 12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1919-350G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005883 | ||||||
chr2:206005887
|
A | G | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1919-354T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005887 | ||||||
chr2:206005895
|
A | T | 1 | a0001c0003t0002g0127 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1919-362T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005895 | ||||||
chr2:206006039
|
C | G | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1919-506G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006039 | ||||||
chr2:206006060
|
C | T | 267 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(264): Show | 270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1919-527G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006060 | ||||||
chr2:206006277
|
C | CCTGAAAT others(3): Show |
1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1919-745_1919-744i others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006277 | ||||||
chr2:206006291
|
G | A | 1 | a0002c0002t0001g0166 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1919-758C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006291 | ||||||
chr2:206006316
|
C | T | 3 | a0001c0001t0002g0230a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG04115.hp2 NA18947.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1919-783G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006316 | ||||||
chr2:206006343
|
A | C | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1919-810T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006343 | ||||||
chr2:206006437
|
C | T | 1 | a0002c0002t0001g0143 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1918+847G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006437 | ||||||
chr2:206006477
|
G | A | 107 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1918+807C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006477 | ||||||
chr2:206006575
|
C | T | 2 | a0001c0001t0003g0079a0001c0001t0029g0063 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1918+709G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006575 | ||||||
chr2:206006576
|
G | A | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1918+708C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006576 | ||||||
chr2:206006640
|
G | A | 1 | a0001c0001t0009g0329 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1918+644C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006640 | ||||||
chr2:206006661
|
C | T | 1 | a0001c0003t0002g0247 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1918+623G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006661 | ||||||
chr2:206006678
|
A | T | 1 | a0003c0007t0001g0163 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1918+606T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006678 | ||||||
chr2:206006682
|
C | CA | 31 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1918+601dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006682 | ||||||
chr2:206006682
|
CA | C | 29 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(26): Show | 30 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1918+601delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006682 | ||||||
chr2:206006734
|
C | T | 238 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(235): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1918+550G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006734 | ||||||
chr2:206006746
|
C | T | 89 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(86): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1918+538G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006746 | ||||||
chr2:206006791
|
A | G | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1918+493T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006791 | ||||||
chr2:206006818
|
G | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1918+466C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006818 | ||||||
chr2:206006867
|
C | T | 20 | a0002c0002t0001g0091a0002c0002t0001g0092a0002c0002t0001g0094others(17): Show | 20 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1918+417G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006867 | ||||||
chr2:206006939
|
C | T | 1 | a0002c0010t0055g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1918+345G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006939 | ||||||
chr2:206007093
|
T | C | 9 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(6): Show | 9 | HG02135.hp2 NA18940.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.1918+191A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206007093 | ||||||
chr2:206007754
|
G | A | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1761-313C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007754 | ||||||
chr2:206007765
|
T | C | 107 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1761-324A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007765 | ||||||
chr2:206007832
|
AC | A | 213 | a0001c0001t0002g0033a0001c0001t0002g0230a0001c0001t0003g0002others(210): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1761-392delG | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007832 | ||||||
chr2:206007833
|
C | A | 105 | a0001c0001t0002g0208a0001c0001t0003g0069a0001c0001t0003g0090others(102): Show | 106 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1761-392G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007833 | ||||||
chr2:206007835
|
A | C | 3 | a0002c0005t0002g0190a0002c0005t0002g0327a0002c0005t0006g0328 | 3 | HG02258.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1761-394T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007835 | ||||||
chr2:206007877
|
T | A | 108 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(105): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1761-436A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007877 | ||||||
chr2:206007893
|
A | G | 1 | a0001c0004t0007g0221 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1761-452T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007893 | ||||||
chr2:206007899
|
G | A | 1 | a0001c0003t0002g0290 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1761-458C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007899 | ||||||
chr2:206007938
|
A | T | 1 | a0001c0003t0006g0291 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1761-497T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007938 | ||||||
chr2:206008003
|
CAG | C | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1761-564_1761-563d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008003 | ||||||
chr2:206008045
|
A | G | 89 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(86): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1761-604T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008045 | ||||||
chr2:206008203
|
C | T | 1 | a0001c0003t0002g0290 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1761-762G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008203 | ||||||
chr2:206008282
|
C | CT | 113 | a0001c0001t0003g0057a0001c0001t0003g0067a0001c0001t0003g0090others(110): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1761-842dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008282 | ||||||
chr2:206008282
|
C | CTT | 6 | a0002c0002t0001g0140a0002c0002t0001g0150a0002c0002t0001g0170others(3): Show | 6 | HG02145.hp2 HG03516.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1761-843_1761-842d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008282 | ||||||
chr2:206008429
|
C | T | 1 | a0001c0001t0009g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1761-988G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008429 | ||||||
chr2:206008487
|
G | A | 1 | a0005c0015t0016g0324 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1761-1046C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008487 | ||||||
chr2:206008789
|
C | T | 1 | a0001c0001t0050g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1760+788G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008789 | ||||||
chr2:206008801
|
T | C | 96 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(93): Show | 98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1760+776A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008801 | ||||||
chr2:206008841
|
G | A | 20 | a0002c0002t0001g0091a0002c0002t0001g0092a0002c0002t0001g0094others(17): Show | 20 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1760+736C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008841 | ||||||
chr2:206008993
|
A | G | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0059others(1): Show | 4 | HG00323.hp2 HG00741.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1760+584T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008993 | ||||||
chr2:206009042
|
G | T | 3 | a0002c0005t0002g0190a0002c0005t0002g0327a0002c0005t0006g0328 | 3 | HG02258.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1760+535C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206009042 | ||||||
chr2:206009171
|
G | A | 3 | a0002c0002t0001g0128a0002c0002t0001g0170a0002c0002t0049g0145 | 3 | HG02145.hp2 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1760+406C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206009171 | ||||||
chr2:206009277
|
G | A | 251 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(248): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1760+300C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206009277 | ||||||
chr2:206009358
|
C | CA | 216 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(213): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1760+218_1760+219i others(3): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206009358 | ||||||
chr2:206009482
|
C | T | 1 | a0001c0001t0026g0004 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1760+95G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206009482 | ||||||
chr2:206009842
|
A | G | 1 | a0002c0002t0058g0102 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1543-48T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206009842 | ||||||
chr2:206009856
|
T | C | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1543-62A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206009856 | ||||||
chr2:206010062
|
T | TAC | 17 | a0001c0001t0041g0213a0001c0001t0042g0031a0001c0003t0002g0247others(14): Show | 17 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1543-270_1543-269d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010062 | ||||||
chr2:206010062
|
T | TACAC | 4 | a0001c0001t0009g0209a0001c0001t0009g0211a0001c0003t0002g0286others(1): Show | 4 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-272_1543-269d others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010062 | ||||||
chr2:206010062
|
TACACACA others(3): Show |
T | 1 | a0002c0002t0001g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1543-278_1543-269d others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010062 | ||||||
chr2:206010083
|
A | ACACACAC others(19): Show |
1 | a0001c0008t0019g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1543-290_1543-289i others(28): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | ||||||
chr2:206010083
|
A | ACACACAC others(15): Show |
2 | a0001c0001t0003g0282a0001c0008t0019g0205 | 2 | HG02165.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1543-290_1543-289i others(24): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | ||||||
chr2:206010083
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0003g0073 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1543-290_1543-289i others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | ||||||
chr2:206010083
|
A | ACACACAC others(9): Show |
35 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(32): Show | 36 | HG00673.hp2 HG00741.hp2 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.1543-290_1543-289i others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | ||||||
chr2:206010083
|
A | ACACACAC others(7): Show |
17 | a0001c0001t0003g0047a0001c0001t0003g0049a0001c0001t0003g0057others(14): Show | 17 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.1543-290_1543-289i others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | ||||||
chr2:206010083
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-290_1543-289i others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | ||||||
chr2:206010083
|
A | ACACACAC others(5): Show |
6 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0004g0020others(3): Show | 6 | HG01081.hp1 HG01106.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-290_1543-289i others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | ||||||
chr2:206010083
|
A | ACACACAC others(3): Show |
26 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(23): Show | 27 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1543-290_1543-289i others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | ||||||
chr2:206010122
|
G | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1543-328C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010122 | ||||||
chr2:206010285
|
A | G | 1 | a0001c0001t0013g0030 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1543-491T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010285 | ||||||
chr2:206010397
|
C | T | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1543-603G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010397 | ||||||
chr2:206010839
|
G | A | 89 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(86): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1543-1045C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010839 | ||||||
chr2:206010844
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1543-1050C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010844 | ||||||
chr2:206010937
|
G | T | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-1143C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010937 | ||||||
chr2:206011078
|
C | CA | 9 | a0001c0001t0002g0230a0001c0001t0041g0213a0001c0003t0002g0294others(6): Show | 9 | HG00621.hp1 HG00642.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1543-1285dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011078 | ||||||
chr2:206011078
|
CA | C | 87 | a0001c0001t0003g0002a0001c0001t0003g0040a0001c0001t0003g0042others(84): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1543-1285delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011078 | ||||||
chr2:206011101
|
A | G | 1 | a0001c0003t0002g0318 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1543-1307T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011101 | ||||||
chr2:206011205
|
G | A | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1543-1411C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011205 | ||||||
chr2:206011208
|
C | G | 3 | a0001c0001t0009g0209a0001c0001t0009g0210a0001c0001t0009g0211 | 3 | HG02055.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1543-1414G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011208 | ||||||
chr2:206011241
|
C | G | 83 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(80): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1543-1447G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011241 | ||||||
chr2:206011304
|
A | G | 4 | a0001c0003t0002g0294a0001c0003t0002g0302a0001c0003t0002g0304others(1): Show | 4 | HG01361.hp1 HG01515.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-1510T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011304 | ||||||
chr2:206011535
|
A | G | 108 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(105): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1543-1741T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011535 | ||||||
chr2:206011944
|
T | C | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1543-2150A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011944 | ||||||
chr2:206011967
|
T | C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-2173A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011967 | ||||||
chr2:206011977
|
G | A | 2 | a0001c0003t0002g0259a0001c0003t0002g0289 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1543-2183C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011977 | ||||||
chr2:206012002
|
C | A | 13 | a0001c0001t0002g0230a0001c0001t0005g0087a0001c0001t0005g0088others(10): Show | 13 | HG00423.hp2 HG00558.hp1 HG04115.hp2 others(10): Show |
intron_variant | MODIFIER | c.1543-2208G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012002 | ||||||
chr2:206012003
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-2209C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012003 | ||||||
chr2:206012007
|
A | T | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-2213T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012007 | ||||||
chr2:206012032
|
G | A | 1 | a0002c0005t0040g0326 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1543-2238C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012032 | ||||||
chr2:206012089
|
G | A | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1543-2295C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012089 | ||||||
chr2:206012202
|
A | G | 252 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1543-2408T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012202 | ||||||
chr2:206012277
|
A | C | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1543-2483T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012277 | ||||||
chr2:206012347
|
G | A | 89 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(86): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1543-2553C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012347 | ||||||
chr2:206012436
|
C | A | 1 | a0001c0003t0002g0294 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1543-2642G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012436 | ||||||
chr2:206012476
|
A | T | 7 | a0002c0002t0001g0107a0002c0002t0001g0123a0002c0002t0001g0138others(4): Show | 7 | HG00642.hp2 HG01346.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543-2682T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012476 | ||||||
chr2:206012574
|
T | C | 1 | a0001c0003t0002g0306 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1543-2780A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012574 | ||||||
chr2:206012588
|
T | C | 326 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(323): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1543-2794A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012588 | ||||||
chr2:206012605
|
C | T | 1 | a0001c0004t0037g0204 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1543-2811G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012605 | ||||||
chr2:206012867
|
C | CA | 41 | a0001c0001t0002g0033a0001c0001t0002g0230a0001c0001t0005g0087others(38): Show | 41 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1543-3074dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012867 | ||||||
chr2:206012867
|
C | CAA | 33 | a0001c0001t0002g0208a0001c0001t0004g0001a0001c0001t0004g0011others(30): Show | 34 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1543-3075_1543-307 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012867 | ||||||
chr2:206012867
|
C | CAAA | 59 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(56): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1543-3076_1543-307 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012867 | ||||||
chr2:206012867
|
C | CAAAA | 9 | a0001c0001t0003g0044a0001c0001t0003g0055a0001c0001t0003g0065others(6): Show | 9 | HG01081.hp1 HG02523.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1543-3077_1543-307 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012867 | ||||||
chr2:206012976
|
CTT | C | 24 | a0001c0001t0002g0230a0001c0001t0005g0087a0001c0001t0005g0088others(21): Show | 24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1543-3184_1543-318 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012976 | ||||||
chr2:206012993
|
C | T | 2 | a0001c0001t0041g0213a0001c0001t0042g0031 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1543-3199G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012993 | ||||||
chr2:206013056
|
C | A | 2 | a0001c0003t0002g0279a0001c0003t0002g0285 | 2 | NA18612.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1543-3262G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013056 | ||||||
chr2:206013276
|
A | G | 1 | a0001c0001t0003g0068 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1543-3482T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013276 | ||||||
chr2:206013289
|
T | C | 2 | a0001c0001t0003g0044a0002c0002t0001g0135 | 2 | NA19010.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1543-3495A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013289 | ||||||
chr2:206013456
|
A | G | 1 | a0001c0001t0003g0154 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1543-3662T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013456 | ||||||
chr2:206013551
|
C | CA | 108 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(105): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1543-3758dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013551 | ||||||
chr2:206013628
|
T | G | 1 | a0001c0003t0002g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1543-3834A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013628 | ||||||
chr2:206013726
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-3932C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013726 | ||||||
chr2:206013848
|
T | TA | 34 | a0001c0001t0002g0230a0001c0001t0005g0232a0001c0001t0005g0233others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1542+3831dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013848 | ||||||
chr2:206013848
|
TA | T | 16 | a0001c0001t0002g0033a0001c0001t0003g0041a0001c0001t0013g0030others(13): Show | 16 | HG01070.hp2 HG01109.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1542+3831delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013848 | ||||||
chr2:206013848
|
TAA | T | 92 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(89): Show | 94 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1542+3830_1542+383 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013848 | ||||||
chr2:206013923
|
C | T | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1542+3757G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013923 | ||||||
chr2:206013943
|
G | A | 95 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(92): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1542+3737C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013943 | ||||||
chr2:206014089
|
C | T | 1 | a0002c0002t0001g0196 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1542+3591G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014089 | ||||||
chr2:206014157
|
CA | C | 42 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(39): Show | 42 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1542+3522delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014157 | ||||||
chr2:206014157
|
CAA | C | 130 | a0001c0001t0002g0033a0001c0001t0009g0210a0001c0001t0013g0030others(127): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1542+3521_1542+352 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014157 | ||||||
chr2:206014157
|
CAAA | C | 92 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(89): Show | 94 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1542+3520_1542+352 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014157 | ||||||
chr2:206014157
|
CAAAA | C | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+3519_1542+352 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014157 | ||||||
chr2:206014237
|
T | C | 1 | a0002c0002t0001g0138 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1542+3443A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014237 | ||||||
chr2:206014541
|
C | T | 1 | a0001c0001t0027g0009 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1542+3139G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014541 | ||||||
chr2:206014729
|
T | C | 252 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1542+2951A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014729 | ||||||
chr2:206014742
|
C | A | 1 | a0002c0005t0002g0190 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1542+2938G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014742 | ||||||
chr2:206014820
|
A | G | 110 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1542+2860T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014820 | ||||||
chr2:206014836
|
T | C | 1 | a0002c0002t0001g0197 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1542+2844A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014836 | ||||||
chr2:206014937
|
A | G | 23 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(20): Show | 23 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1542+2743T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014937 | ||||||
chr2:206015110
|
T | C | 1 | a0001c0001t0018g0008 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1542+2570A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015110 | ||||||
chr2:206015387
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1542+2293C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015387 | ||||||
chr2:206015404
|
A | G | 96 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(93): Show | 98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1542+2276T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015404 | ||||||
chr2:206015622
|
C | G | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+2058G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015622 | ||||||
chr2:206015647
|
G | C | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1542+2033C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015647 | ||||||
chr2:206015655
|
C | T | 1 | a0001c0004t0011g0219 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1542+2025G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015655 | ||||||
chr2:206015747
|
C | A | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+1933G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015747 | ||||||
chr2:206015759
|
C | T | 25 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1542+1921G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015759 | ||||||
chr2:206015800
|
T | G | 2 | a0002c0002t0001g0169a0002c0002t0001g0172 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1542+1880A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015800 | ||||||
chr2:206015869
|
A | G | 111 | a0001c0003t0014g0319a0001c0006t0001g0110a0001c0006t0001g0122others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1542+1811T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015869 | ||||||
chr2:206015941
|
G | A | 109 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1542+1739C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015941 | ||||||
chr2:206016003
|
C | T | 2 | a0001c0001t0041g0213a0001c0001t0042g0031 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1542+1677G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016003 | ||||||
chr2:206016071
|
A | T | 1 | a0001c0001t0064g0331 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1542+1609T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016071 | ||||||
chr2:206016166
|
C | CTA | 20 | a0002c0002t0001g0091a0002c0002t0001g0092a0002c0002t0001g0094others(17): Show | 20 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1542+1512_1542+151 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016166 | ||||||
chr2:206016373
|
C | T | 110 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1542+1307G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016373 | ||||||
chr2:206016529
|
C | T | 88 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(85): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1542+1151G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016529 | ||||||
chr2:206016626
|
C | G | 1 | a0001c0003t0002g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1542+1054G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016626 | ||||||
chr2:206016643
|
C | T | 12 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212others(9): Show | 12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1542+1037G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016643 | ||||||
chr2:206016758
|
G | A | 1 | a0001c0003t0002g0267 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1542+922C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016758 | ||||||
chr2:206017204
|
C | T | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1542+476G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206017204 | ||||||
chr2:206017306
|
G | T | 4 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0061others(1): Show | 4 | HG01099.hp2 HG01109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1542+374C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206017306 | ||||||
chr2:206017504
|
C | A | 1 | a0002c0002t0001g0155 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1542+176G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206017504 | ||||||
chr2:206017526
|
C | T | 1 | a0001c0003t0002g0279 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1542+154G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206017526 | ||||||
chr2:206018236
|
G | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-423C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206018236 | ||||||
chr2:206018245
|
A | G | 109 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1409-432T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206018245 | ||||||
chr2:206018270
|
G | A | 1 | a0001c0001t0005g0087 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1409-457C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206018270 | ||||||
chr2:206018486
|
T | G | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-673A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206018486 | ||||||
chr2:206018654
|
C | G | 3 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212 | 3 | HG01123.hp2 HG03710.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1409-841G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206018654 | ||||||
chr2:206019124
|
T | C | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1408+612A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206019124 | ||||||
chr2:206019196
|
A | G | 1 | a0001c0001t0009g0209 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1408+540T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206019196 | ||||||
chr2:206019403
|
A | G | 1 | a0001c0001t0003g0040 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1408+333T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206019403 | ||||||
chr2:206019571
|
G | C | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1408+165C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206019571 | ||||||
chr2:206019588
|
A | T | 1 | a0001c0003t0014g0319 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1408+148T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206019588 | ||||||
chr2:206019850
|
G | C | 1 | a0001c0003t0006g0295 | 1 | NA19009.hp1 | splice_region_variant&intron_variant | LOW | c.1299-5C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206019850 | ||||||
chr2:206019871
|
AT | A | 88 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(85): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1299-27delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206019871 | ||||||
chr2:206020002
|
G | A | 12 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212others(9): Show | 12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1299-157C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020002 | ||||||
chr2:206020068
|
G | C | 252 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1299-223C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020068 | ||||||
chr2:206020089
|
G | GT | 245 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(242): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1299-245dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020089 | ||||||
chr2:206020115
|
T | C | 1 | a0001c0001t0004g0016 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1299-270A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020115 | ||||||
chr2:206020469
|
C | A | 214 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(211): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1299-624G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020469 | ||||||
chr2:206020704
|
A | C | 2 | a0004c0009t0007g0217a0004c0009t0011g0215 | 2 | HG01257.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1299-859T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020704 | ||||||
chr2:206020791
|
A | C | 1 | a0002c0005t0002g0190 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1299-946T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020791 | ||||||
chr2:206021006
|
C | G | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1299-1161G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021006 | ||||||
chr2:206021329
|
G | A | 109 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1299-1484C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021329 | ||||||
chr2:206021497
|
T | C | 2 | a0001c0001t0003g0067a0006c0014t0003g0075 | 2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1299-1652A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021497 | ||||||
chr2:206021693
|
A | G | 5 | a0001c0001t0016g0322a0001c0001t0016g0323a0001c0008t0019g0205others(2): Show | 5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299-1848T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021693 | ||||||
chr2:206021776
|
T | C | 2 | a0002c0002t0001g0125a0002c0002t0001g0126 | 2 | HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1299-1931A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021776 | ||||||
chr2:206021889
|
C | G | 1 | a0001c0003t0002g0280 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1299-2044G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021889 | ||||||
chr2:206022041
|
C | A | 203 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(200): Show | 206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1299-2196G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022041 | ||||||
chr2:206022250
|
C | T | 3 | a0001c0001t0005g0224a0001c0001t0005g0227a0001c0001t0005g0234 | 3 | NA18984.hp2 NA19002.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1299-2405G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022250 | ||||||
chr2:206022375
|
A | G | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1299-2530T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022375 | ||||||
chr2:206022465
|
C | G | 110 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1299-2620G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022465 | ||||||
chr2:206022509
|
A | T | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1299-2664T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022509 | ||||||
chr2:206022615
|
A | G | 1 | a0001c0001t0005g0089 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1299-2770T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022615 | ||||||
chr2:206022771
|
T | C | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1299-2926A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022771 | ||||||
chr2:206022773
|
G | T | 2 | a0001c0001t0004g0014a0001c0001t0004g0028 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1299-2928C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022773 | ||||||
chr2:206022787
|
C | T | 1 | a0007c0012t0002g0252 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1299-2942G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022787 | ||||||
chr2:206022798
|
C | T | 1 | a0002c0002t0001g0093 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1299-2953G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022798 | ||||||
chr2:206022862
|
T | G | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(2): Show | 5 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299-3017A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022862 | ||||||
chr2:206022968
|
G | T | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1299-3123C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022968 | ||||||
chr2:206023125
|
C | T | 1 | a0001c0004t0037g0204 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1299-3280G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023125 | ||||||
chr2:206023126
|
G | A | 107 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1299-3281C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023126 | ||||||
chr2:206023141
|
C | A | 3 | a0002c0005t0002g0327a0002c0005t0006g0328a0002c0005t0040g0326 | 3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1299-3296G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023141 | ||||||
chr2:206023255
|
T | C | 1 | a0001c0001t0004g0018 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1299-3410A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023255 | ||||||
chr2:206023438
|
C | T | 1 | a0001c0001t0026g0004 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1299-3593G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023438 | ||||||
chr2:206023540
|
G | A | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1299-3695C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023540 | ||||||
chr2:206023554
|
A | G | 252 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1299-3709T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023554 | ||||||
chr2:206023631
|
C | T | 18 | a0001c0001t0002g0230a0001c0001t0005g0087a0001c0001t0005g0088others(15): Show | 18 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1299-3786G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023631 | ||||||
chr2:206023680
|
T | TA | 45 | a0001c0001t0003g0041a0001c0001t0004g0001a0001c0001t0004g0011others(42): Show | 46 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.1299-3836dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023680 | ||||||
chr2:206023680
|
TA | T | 13 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(10): Show | 13 | HG01070.hp2 HG01255.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1299-3836delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023680 | ||||||
chr2:206023871
|
T | C | 5 | a0001c0001t0016g0322a0001c0001t0016g0323a0001c0008t0019g0205others(2): Show | 5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299-4026A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023871 | ||||||
chr2:206024128
|
A | G | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1298+3983T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206024128 | ||||||
chr2:206024295
|
G | C | 1 | a0001c0004t0011g0214 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1298+3816C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206024295 | ||||||
chr2:206024409
|
A | C | 3 | a0001c0001t0015g0006a0001c0001t0015g0007a0001c0001t0015g0010 | 3 | HG00735.hp2 HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1298+3702T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206024409 | ||||||
chr2:206024778
|
C | T | 43 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(40): Show | 44 | HG00323.hp2 HG00673.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.1298+3333G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206024778 | ||||||
chr2:206025090
|
G | T | 109 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1298+3021C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025090 | ||||||
chr2:206025386
|
A | G | 252 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1298+2725T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025386 | ||||||
chr2:206025389
|
G | A | 1 | a0001c0001t0004g0022 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1298+2722C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025389 | ||||||
chr2:206025397
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1298+2714C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025397 | ||||||
chr2:206025472
|
G | A | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1298+2639C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025472 | ||||||
chr2:206025506
|
C | T | 21 | a0001c0003t0002g0127a0001c0003t0002g0160a0001c0003t0002g0171others(18): Show | 21 | HG00438.hp1 HG02071.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1298+2605G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025506 | ||||||
chr2:206025528
|
C | CAA | 11 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(8): Show | 11 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1298+2581_1298+258 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025528 | ||||||
chr2:206025528
|
C | CAAAAA | 14 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(11): Show | 15 | HG00738.hp1 HG01123.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1298+2578_1298+258 others(9): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025528 | ||||||
chr2:206025528
|
C | CAAAAAA | 6 | a0001c0001t0004g0018a0001c0001t0015g0006a0001c0001t0015g0007others(3): Show | 6 | HG00741.hp1 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1298+2577_1298+258 others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025528 | ||||||
chr2:206025528
|
C | CAAAAAAA others(5): Show |
2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1298+2571_1298+258 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025528 | ||||||
chr2:206025528
|
CAA | C | 9 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212others(6): Show | 9 | HG01123.hp2 HG01175.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1298+2581_1298+258 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025528 | ||||||
chr2:206025538
|
A | AATATATA others(5): Show |
1 | a0002c0016t0036g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1298+2572_1298+257 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025538 | ||||||
chr2:206025538
|
A | AATATATA others(9): Show |
1 | a0002c0002t0001g0194 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1298+2572_1298+257 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025538 | ||||||
chr2:206025540
|
A | AATATATA others(3): Show |
3 | a0002c0002t0001g0094a0002c0002t0001g0136a0002c0002t0001g0148 | 3 | NA19004.hp1 NA19011.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1298+2570_1298+257 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025540 | ||||||
chr2:206025540
|
A | AATATATA others(5): Show |
3 | a0002c0002t0001g0103a0002c0002t0001g0123a0002c0002t0001g0184 | 3 | HG00280.hp1 HG01346.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1298+2570_1298+257 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025540 | ||||||
chr2:206025540
|
A | AATATATA others(7): Show |
1 | a0002c0005t0002g0327 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1298+2570_1298+257 others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025540 | ||||||
chr2:206025540
|
A | AATATATA others(21): Show |
1 | a0002c0002t0001g0186 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1298+2570_1298+257 others(32): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025540 | ||||||
chr2:206025540
|
A | T | 5 | a0001c0001t0003g0067a0001c0001t0012g0084a0001c0001t0012g0086others(2): Show | 5 | HG00621.hp1 HG02738.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1298+2571T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025540 | ||||||
chr2:206025542
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0004g0023 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(29): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAAAAAA others(17): Show |
2 | a0001c0001t0004g0014a0001c0001t0004g0028 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(28): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0064g0331 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(32): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0025g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(32): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAAAAAA others(9): Show |
3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAATATA others(1): Show |
15 | a0001c0003t0002g0297a0001c0003t0002g0303a0002c0002t0001g0003others(12): Show | 16 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAATATA others(3): Show |
4 | a0002c0002t0001g0092a0002c0002t0001g0098a0002c0002t0001g0100others(1): Show | 4 | HG02165.hp1 HG02523.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAATATA others(5): Show |
2 | a0002c0002t0001g0120a0002c0002t0001g0150 | 2 | HG03579.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAATATA others(7): Show |
1 | a0002c0002t0039g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAATATA others(9): Show |
2 | a0002c0002t0001g0114a0002c0002t0001g0115 | 2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAATATA others(11): Show |
1 | a0002c0002t0047g0117 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(22): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAAATATA others(15): Show |
1 | a0002c0002t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(26): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAATATAT others(4): Show |
1 | a0002c0002t0001g0187 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(15): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAATATAT others(14): Show |
1 | a0002c0002t0001g0170 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(25): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AAT | 12 | a0001c0001t0003g0083a0001c0001t0003g0095a0001c0001t0003g0282others(9): Show | 12 | HG01070.hp2 HG01255.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.1298+2567_1298+256 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AATAT | 12 | a0001c0001t0003g0039a0001c0001t0003g0055a0001c0001t0003g0060others(9): Show | 12 | HG00099.hp2 HG00673.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1298+2565_1298+256 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AATATAT | 7 | a0001c0001t0031g0246a0001c0003t0006g0255a0001c0003t0006g0299others(4): Show | 7 | HG01928.hp2 HG02293.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1298+2563_1298+256 others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AATATATA others(1): Show |
37 | a0001c0001t0028g0052a0001c0003t0002g0276a0001c0003t0002g0310others(34): Show | 37 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1298+2561_1298+256 others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AATATATA others(3): Show |
15 | a0001c0003t0002g0308a0001c0003t0017g0307a0002c0002t0001g0096others(12): Show | 15 | HG00423.hp1 HG01168.hp2 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.1298+2559_1298+256 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AATATATA others(5): Show |
6 | a0001c0003t0002g0273a0002c0002t0001g0156a0002c0002t0001g0183others(3): Show | 6 | HG00099.hp1 HG00735.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1298+2557_1298+256 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AATATATA others(7): Show |
4 | a0002c0002t0001g0147a0002c0002t0001g0167a0002c0005t0006g0328others(1): Show | 4 | HG03098.hp1 NA18945.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1298+2555_1298+256 others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | AATATATA others(9): Show |
3 | a0002c0002t0001g0106a0002c0002t0001g0196a0002c0002t0010g0109 | 3 | HG00140.hp2 HG04199.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1298+2553_1298+256 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | ATATATAT others(4): Show |
2 | a0002c0002t0001g0149a0002c0002t0001g0198 | 2 | HG02735.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(15): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
A | T | 23 | a0001c0001t0003g0043a0001c0001t0003g0067a0001c0001t0012g0084others(20): Show | 23 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1298+2569T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025542
|
AATAT | A | 13 | a0001c0001t0005g0089a0001c0001t0005g0224a0001c0001t0005g0227others(10): Show | 13 | HG00423.hp2 HG00642.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1298+2565_1298+256 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | ||||||
chr2:206025543
|
AT | A | 11 | a0001c0001t0003g0065a0001c0001t0003g0076a0001c0001t0003g0085others(8): Show | 11 | HG00673.hp2 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1298+2567delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025543 | ||||||
chr2:206025543
|
ATATAT | A | 5 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0233others(2): Show | 5 | HG00558.hp1 NA18960.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1298+2563_1298+256 others(9): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025543 | ||||||
chr2:206025544
|
T | A | 49 | a0001c0001t0002g0033a0001c0001t0003g0047a0001c0001t0003g0048others(46): Show | 50 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1298+2567A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025544 | ||||||
chr2:206025546
|
T | A | 41 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0004g0001others(38): Show | 42 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1298+2565A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025546 | ||||||
chr2:206025548
|
T | A | 44 | a0001c0001t0002g0033a0001c0001t0004g0001a0001c0001t0004g0011others(41): Show | 45 | HG00423.hp2 HG00642.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1298+2563A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025548 | ||||||
chr2:206025550
|
T | A | 25 | a0001c0001t0002g0033a0001c0001t0004g0001a0001c0001t0004g0011others(22): Show | 26 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1298+2561A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025550 | ||||||
chr2:206025552
|
T | A | 23 | a0001c0001t0002g0033a0001c0001t0004g0001a0001c0001t0004g0011others(20): Show | 24 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1298+2559A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025552 | ||||||
chr2:206025554
|
T | A | 15 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(12): Show | 16 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1298+2557A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025554 | ||||||
chr2:206025556
|
T | A | 4 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0025others(1): Show | 4 | HG01256.hp2 HG01516.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1298+2555A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025556 | ||||||
chr2:206025568
|
T | TATATATA others(9): Show |
1 | a0002c0002t0001g0175 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1298+2542_1298+254 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025568 | ||||||
chr2:206025568
|
TAA | T | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1298+2541_1298+254 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025568 | ||||||
chr2:206025570
|
A | T | 89 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(86): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1298+2541T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025570 | ||||||
chr2:206025636
|
C | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1298+2475G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025636 | ||||||
chr2:206025721
|
G | A | 2 | a0002c0010t0001g0116a0002c0010t0055g0176 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1298+2390C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025721 | ||||||
chr2:206025892
|
T | C | 36 | a0001c0003t0002g0257a0001c0003t0002g0260a0001c0003t0002g0273others(33): Show | 36 | HG00099.hp2 HG00621.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1298+2219A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025892 | ||||||
chr2:206026090
|
G | T | 2 | a0004c0009t0007g0217a0004c0009t0011g0215 | 2 | HG01257.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1298+2021C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026090 | ||||||
chr2:206026124
|
C | T | 88 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(85): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1298+1987G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026124 | ||||||
chr2:206026272
|
G | A | 1 | a0001c0001t0038g0287 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1298+1839C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026272 | ||||||
chr2:206026285
|
C | T | 1 | a0001c0003t0002g0304 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1298+1826G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026285 | ||||||
chr2:206026312
|
A | G | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1298+1799T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026312 | ||||||
chr2:206026414
|
C | T | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1298+1697G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026414 | ||||||
chr2:206026428
|
C | T | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1298+1683G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026428 | ||||||
chr2:206026557
|
A | T | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1298+1554T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026557 | ||||||
chr2:206027112
|
A | C | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1298+999T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027112 | ||||||
chr2:206027145
|
C | T | 1 | a0001c0001t0004g0015 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1298+966G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027145 | ||||||
chr2:206027156
|
G | GCA | 66 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(63): Show | 67 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.1298+953_1298+954d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | ||||||
chr2:206027156
|
G | GCACA | 4 | a0001c0001t0003g0068a0001c0003t0002g0290a0001c0003t0002g0297others(1): Show | 4 | HG00280.hp2 HG01175.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1298+951_1298+954d others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | ||||||
chr2:206027156
|
G | GCACACA | 8 | a0001c0001t0003g0047a0001c0001t0003g0069a0001c0001t0003g0070others(5): Show | 8 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1298+949_1298+954d others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | ||||||
chr2:206027156
|
GCA | G | 156 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(153): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1298+953_1298+954d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | ||||||
chr2:206027156
|
GCACA | G | 14 | a0001c0001t0031g0246a0001c0004t0007g0202a0001c0004t0007g0203others(11): Show | 14 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1298+951_1298+954d others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | ||||||
chr2:206027156
|
GCACACAC others(3): Show |
G | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1298+945_1298+954d others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | ||||||
chr2:206027160
|
A | G | 1 | a0002c0005t0040g0326 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1298+951T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027160 | ||||||
chr2:206027224
|
TTCTC | T | 22 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(19): Show | 22 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1298+883_1298+886d others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027224 | ||||||
chr2:206027597
|
A | G | 1 | a0001c0001t0013g0207 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1298+514T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027597 | ||||||
chr2:206027682
|
C | T | 95 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(92): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1298+429G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027682 | ||||||
chr2:206027754
|
T | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1298+357A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027754 | ||||||
chr2:206027780
|
T | C | 1 | a0001c0003t0006g0288 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1298+331A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027780 | ||||||
chr2:206028565
|
T | C | 1 | a0002c0010t0001g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1074-230A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206028565 | ||||||
chr2:206028884
|
G | T | 1 | a0002c0002t0047g0117 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1074-549C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206028884 | ||||||
chr2:206028888
|
T | G | 1 | a0001c0001t0022g0032 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1074-553A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206028888 | ||||||
chr2:206028894
|
T | G | 57 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(54): Show | 58 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1074-559A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206028894 | ||||||
chr2:206028895
|
T | G | 1 | a0001c0001t0009g0209 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1074-560A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206028895 | ||||||
chr2:206029005
|
A | G | 1 | a0001c0003t0006g0298 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1074-670T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206029005 | ||||||
chr2:206029236
|
A | T | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1074-901T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206029236 | ||||||
chr2:206029591
|
ATTC | A | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1074-1259_1074-125 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206029591 | ||||||
chr2:206029602
|
C | T | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-1267G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206029602 | ||||||
chr2:206029845
|
G | C | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-1510C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206029845 | ||||||
chr2:206030078
|
G | A | 1 | a0001c0001t0009g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1074-1743C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206030078 | ||||||
chr2:206030265
|
A | T | 4 | a0001c0003t0002g0314a0001c0003t0002g0315a0001c0003t0006g0312others(1): Show | 4 | HG02486.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-1930T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206030265 | ||||||
chr2:206030462
|
C | CA | 113 | a0001c0001t0005g0224a0001c0001t0005g0234a0001c0003t0002g0160others(110): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1074-2128dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206030462 | ||||||
chr2:206030616
|
G | GT | 3 | a0001c0001t0004g0014a0001c0001t0004g0023a0001c0001t0004g0028 | 3 | HG01515.hp1 HG01517.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1074-2282dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206030616 | ||||||
chr2:206030783
|
T | A | 5 | a0001c0001t0016g0322a0001c0001t0016g0323a0001c0008t0019g0205others(2): Show | 5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-2448A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206030783 | ||||||
chr2:206031149
|
G | T | 1 | a0002c0002t0001g0107 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1074-2814C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031149 | ||||||
chr2:206031486
|
A | G | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1074-3151T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031486 | ||||||
chr2:206031597
|
G | A | 1 | a0001c0001t0022g0032 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1074-3262C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031597 | ||||||
chr2:206031676
|
C | T | 2 | a0001c0001t0016g0322a0001c0001t0016g0323 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1074-3341G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031676 | ||||||
chr2:206031711
|
G | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-3376C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031711 | ||||||
chr2:206031904
|
G | A | 1 | a0001c0003t0002g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1074-3569C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031904 | ||||||
chr2:206032138
|
T | G | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1074-3803A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206032138 | ||||||
chr2:206032255
|
C | G | 2 | a0001c0003t0002g0280a0001c0003t0002g0283 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1074-3920G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206032255 | ||||||
chr2:206032333
|
G | A | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1074-3998C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206032333 | ||||||
chr2:206032564
|
G | C | 1 | a0002c0002t0010g0109 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1074-4229C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206032564 | ||||||
chr2:206032665
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1074-4330G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206032665 | ||||||
chr2:206033150
|
A | T | 1 | a0001c0001t0003g0043 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1074-4815T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033150 | ||||||
chr2:206033228
|
G | C | 1 | a0001c0013t0005g0228 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1074-4893C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033228 | ||||||
chr2:206033321
|
T | C | 1 | a0002c0002t0001g0175 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1074-4986A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033321 | ||||||
chr2:206033425
|
C | T | 1 | a0002c0005t0040g0326 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1074-5090G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033425 | ||||||
chr2:206033447
|
T | A | 1 | a0001c0001t0004g0011 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1074-5112A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033447 | ||||||
chr2:206033783
|
A | T | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1074-5448T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033783 | ||||||
chr2:206033980
|
C | G | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1074-5645G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033980 | ||||||
chr2:206034073
|
C | A | 2 | a0002c0010t0001g0116a0002c0010t0055g0176 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1074-5738G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034073 | ||||||
chr2:206034287
|
C | T | 1 | a0002c0002t0001g0161 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1074-5952G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034287 | ||||||
chr2:206034583
|
G | A | 86 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(83): Show | 87 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1074-6248C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034583 | ||||||
chr2:206034605
|
A | T | 1 | a0002c0002t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1074-6270T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034605 | ||||||
chr2:206034674
|
GAACTGGA others(36): Show |
G | 9 | a0002c0002t0001g0093a0002c0002t0001g0097a0002c0002t0001g0134others(6): Show | 9 | HG00639.hp1 HG01074.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074-6382_1074-634 others(47): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034674 | ||||||
chr2:206034746
|
C | G | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1074-6411G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034746 | ||||||
chr2:206034861
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1074-6526T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034861 | ||||||
chr2:206035018
|
A | C | 2 | a0002c0010t0001g0116a0002c0010t0055g0176 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1074-6683T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035018 | ||||||
chr2:206035041
|
C | T | 1 | a0001c0001t0002g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1074-6706G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035041 | ||||||
chr2:206035072
|
A | G | 1 | a0001c0003t0062g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1074-6737T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035072 | ||||||
chr2:206035098
|
C | G | 1 | a0002c0002t0001g0170 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1074-6763G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035098 | ||||||
chr2:206035116
|
T | A | 1 | a0002c0010t0001g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1074-6781A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035116 | ||||||
chr2:206035134
|
G | A | 20 | a0002c0002t0001g0091a0002c0002t0001g0092a0002c0002t0001g0094others(17): Show | 20 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1074-6799C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035134 | ||||||
chr2:206035386
|
AAAT | A | 88 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(85): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1074-7054_1074-705 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035386 | ||||||
chr2:206035487
|
A | G | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1074-7152T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035487 | ||||||
chr2:206035536
|
A | G | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1074-7201T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035536 | ||||||
chr2:206036166
|
A | G | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1074-7831T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206036166 | ||||||
chr2:206036220
|
T | C | 95 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(92): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1074-7885A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206036220 | ||||||
chr2:206036237
|
C | T | 105 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1074-7902G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206036237 | ||||||
chr2:206036301
|
T | C | 1 | a0001c0003t0002g0284 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1074-7966A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206036301 | ||||||
chr2:206036488
|
A | C | 1 | a0001c0001t0002g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1074-8153T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206036488 | ||||||
chr2:206037001
|
T | C | 102 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(99): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1074-8666A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037001 | ||||||
chr2:206037365
|
C | T | 110 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1074-9030G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037365 | ||||||
chr2:206037509
|
A | G | 217 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(214): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1073+8995T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037509 | ||||||
chr2:206037532
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1073+8972C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037532 | ||||||
chr2:206037635
|
A | G | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+8869T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037635 | ||||||
chr2:206037771
|
G | A | 23 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(20): Show | 23 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1073+8733C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037771 | ||||||
chr2:206037886
|
G | A | 1 | a0002c0002t0057g0174 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1073+8618C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037886 | ||||||
chr2:206038124
|
C | T | 206 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(203): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1073+8380G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038124 | ||||||
chr2:206038181
|
T | C | 3 | a0001c0003t0002g0268a0001c0003t0002g0280a0001c0003t0002g0283 | 3 | HG02109.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1073+8323A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038181 | ||||||
chr2:206038214
|
A | G | 1 | a0001c0001t0038g0287 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1073+8290T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038214 | ||||||
chr2:206038485
|
T | C | 2 | a0001c0001t0003g0047a0001c0001t0003g0076 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1073+8019A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038485 | ||||||
chr2:206038578
|
T | C | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1073+7926A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038578 | ||||||
chr2:206038726
|
G | A | 88 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(85): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1073+7778C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038726 | ||||||
chr2:206038792
|
C | A | 107 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1073+7712G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038792 | ||||||
chr2:206039053
|
A | G | 103 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(100): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1073+7451T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039053 | ||||||
chr2:206039060
|
G | A | 2 | a0002c0002t0010g0244a0002c0002t0046g0245 | 2 | NA18989.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1073+7444C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039060 | ||||||
chr2:206039168
|
C | T | 21 | a0001c0001t0002g0230a0001c0001t0005g0087a0001c0001t0005g0088others(18): Show | 21 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1073+7336G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039168 | ||||||
chr2:206039337
|
C | T | 134 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1073+7167G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039337 | ||||||
chr2:206039354
|
G | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+7150C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039354 | ||||||
chr2:206039366
|
C | T | 2 | a0002c0002t0001g0111a0002c0002t0001g0133 | 2 | HG01928.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1073+7138G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039366 | ||||||
chr2:206039414
|
A | C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+7090T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039414 | ||||||
chr2:206039477
|
C | T | 16 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(13): Show | 17 | HG00738.hp1 HG01123.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1073+7027G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039477 | ||||||
chr2:206039530
|
T | C | 3 | a0001c0004t0007g0216a0001c0004t0007g0218a0001c0004t0007g0220 | 3 | HG00639.hp2 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1073+6974A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039530 | ||||||
chr2:206039577
|
T | C | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1073+6927A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039577 | ||||||
chr2:206039608
|
C | T | 1 | a0002c0002t0001g0143 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1073+6896G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039608 | ||||||
chr2:206039609
|
G | A | 1 | a0002c0002t0001g0155 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1073+6895C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039609 | ||||||
chr2:206039810
|
CA | C | 104 | a0001c0001t0003g0040a0001c0001t0004g0019a0001c0001t0024g0013others(101): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1073+6693delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039810 | ||||||
chr2:206039810
|
CAA | C | 99 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(96): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1073+6692_1073+669 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039810 | ||||||
chr2:206039841
|
G | A | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1073+6663C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039841 | ||||||
chr2:206039842
|
A | G | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1073+6662T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039842 | ||||||
chr2:206039969
|
G | A | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+6535C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039969 | ||||||
chr2:206039972
|
A | C | 1 | a0001c0001t0034g0225 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1073+6532T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039972 | ||||||
chr2:206040020
|
C | T | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1073+6484G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040020 | ||||||
chr2:206040021
|
G | A | 1 | a0002c0002t0001g0196 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1073+6483C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040021 | ||||||
chr2:206040118
|
C | A | 1 | a0001c0001t0004g0020 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1073+6386G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040118 | ||||||
chr2:206040154
|
G | A | 1 | a0002c0005t0040g0326 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1073+6350C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040154 | ||||||
chr2:206040206
|
T | C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+6298A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040206 | ||||||
chr2:206040244
|
C | G | 12 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212others(9): Show | 12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1073+6260G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040244 | ||||||
chr2:206040279
|
C | T | 2 | a0001c0001t0041g0213a0001c0001t0042g0031 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1073+6225G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040279 | ||||||
chr2:206040285
|
C | CA | 68 | a0001c0001t0003g0002a0001c0001t0003g0040a0001c0001t0003g0041others(65): Show | 69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1073+6218dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040285 | ||||||
chr2:206040285
|
C | CAA | 37 | a0001c0001t0002g0033a0001c0001t0003g0090a0001c0001t0003g0095others(34): Show | 38 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1073+6217_1073+621 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040285 | ||||||
chr2:206040381
|
A | C | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1073+6123T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040381 | ||||||
chr2:206040385
|
A | G | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1073+6119T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040385 | ||||||
chr2:206040426
|
G | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+6078C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040426 | ||||||
chr2:206040674
|
T | G | 2 | a0001c0003t0002g0270a0001c0003t0023g0258 | 2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1073+5830A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040674 | ||||||
chr2:206040676
|
C | G | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+5828G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040676 | ||||||
chr2:206040697
|
A | G | 95 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(92): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1073+5807T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040697 | ||||||
chr2:206040762
|
T | G | 252 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1073+5742A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040762 | ||||||
chr2:206040806
|
G | A | 1 | a0001c0001t0013g0207 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1073+5698C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040806 | ||||||
chr2:206040808
|
G | A | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1073+5696C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040808 | ||||||
chr2:206040826
|
T | C | 1 | a0001c0001t0003g0072 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1073+5678A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040826 | ||||||
chr2:206040879
|
A | G | 1 | a0001c0001t0003g0054 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1073+5625T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040879 | ||||||
chr2:206040964
|
G | A | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1073+5540C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040964 | ||||||
chr2:206041006
|
C | A | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1073+5498G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041006 | ||||||
chr2:206041009
|
G | T | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1073+5495C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041009 | ||||||
chr2:206041023
|
C | T | 1 | a0001c0001t0013g0030 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1073+5481G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041023 | ||||||
chr2:206041204
|
C | T | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1073+5300G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041204 | ||||||
chr2:206041208
|
TA | T | 213 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(210): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1073+5295delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041208 | ||||||
chr2:206041421
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1073+5083C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041421 | ||||||
chr2:206041459
|
G | A | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+5045C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041459 | ||||||
chr2:206041721
|
C | T | 95 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(92): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1073+4783G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041721 | ||||||
chr2:206041879
|
G | A | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+4625C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041879 | ||||||
chr2:206042073
|
G | A | 1 | a0002c0002t0048g0119 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1073+4431C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042073 | ||||||
chr2:206042210
|
G | A | 1 | a0001c0001t0003g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1073+4294C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042210 | ||||||
chr2:206042508
|
C | G | 8 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(5): Show | 8 | HG02135.hp2 NA18940.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.1073+3996G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042508 | ||||||
chr2:206042532
|
G | A | 150 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(147): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1073+3972C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042532 | ||||||
chr2:206042611
|
G | A | 110 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1073+3893C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042611 | ||||||
chr2:206042656
|
G | C | 2 | a0002c0002t0001g0167a0002c0002t0001g0185 | 2 | NA18945.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1073+3848C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042656 | ||||||
chr2:206042679
|
T | A | 1 | a0002c0002t0046g0245 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1073+3825A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042679 | ||||||
chr2:206042680
|
C | A | 1 | a0002c0002t0046g0245 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1073+3824G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042680 | ||||||
chr2:206042680
|
C | CA | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1073+3823dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042680 | ||||||
chr2:206042680
|
C | CAA | 87 | a0001c0001t0003g0072a0001c0001t0003g0090a0001c0001t0003g0154others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1073+3822_1073+382 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042680 | ||||||
chr2:206042680
|
C | CAAA | 21 | a0002c0002t0001g0091a0002c0002t0001g0092a0002c0002t0001g0094others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.1073+3821_1073+382 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042680 | ||||||
chr2:206042882
|
G | A | 90 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(87): Show | 92 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1073+3622C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042882 | ||||||
chr2:206042907
|
G | C | 39 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(36): Show | 39 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1073+3597C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042907 | ||||||
chr2:206043263
|
C | T | 23 | a0002c0002t0001g0091a0002c0002t0001g0092a0002c0002t0001g0094others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.1073+3241G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043263 | ||||||
chr2:206043330
|
C | T | 5 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0021g0046others(2): Show | 5 | HG01081.hp1 HG01106.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073+3174G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043330 | ||||||
chr2:206043391
|
C | T | 1 | a0002c0002t0001g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1073+3113G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043391 | ||||||
chr2:206043422
|
G | A | 39 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(36): Show | 39 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1073+3082C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043422 | ||||||
chr2:206043519
|
G | A | 19 | a0001c0003t0002g0127a0001c0003t0002g0160a0001c0003t0002g0171others(16): Show | 19 | HG00438.hp1 HG02071.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.1073+2985C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043519 | ||||||
chr2:206043544
|
GTGGCACG others(12): Show |
G | 1 | a0002c0002t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1073+2941_1073+295 others(23): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043544 | ||||||
chr2:206043598
|
C | T | 7 | a0001c0001t0003g0055a0001c0001t0003g0056a0001c0001t0003g0060others(4): Show | 7 | HG02132.hp1 HG02523.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073+2906G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043598 | ||||||
chr2:206043690
|
C | T | 1 | a0001c0001t0003g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1073+2814G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043690 | ||||||
chr2:206043767
|
G | A | 111 | a0001c0001t0031g0246a0001c0006t0001g0110a0001c0006t0001g0122others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1073+2737C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043767 | ||||||
chr2:206043770
|
A | AG | 330 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1073+2733_1073+273 others(5): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043770 | ||||||
chr2:206043772
|
G | C | 330 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1073+2732C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043772 | ||||||
chr2:206044086
|
G | A | 1 | a0002c0005t0040g0326 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1073+2418C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044086 | ||||||
chr2:206044265
|
T | C | 110 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1073+2239A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044265 | ||||||
chr2:206044271
|
G | A | 1 | a0002c0002t0001g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1073+2233C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044271 | ||||||
chr2:206044481
|
T | TA | 26 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(23): Show | 27 | HG00738.hp1 HG01123.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1073+2022dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044481 | ||||||
chr2:206044481
|
T | TAA | 32 | a0001c0001t0041g0213a0001c0003t0002g0286a0002c0002t0001g0091others(29): Show | 32 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1073+2021_1073+202 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044481 | ||||||
chr2:206044481
|
T | TAAA | 78 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(75): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1073+2020_1073+202 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044481 | ||||||
chr2:206044481
|
TA | T | 32 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0004g0028others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1073+2022delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044481 | ||||||
chr2:206044546
|
G | A | 1 | a0001c0003t0002g0318 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1073+1958C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044546 | ||||||
chr2:206044663
|
T | C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+1841A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044663 | ||||||
chr2:206044773
|
C | T | 4 | a0001c0001t0009g0209a0001c0001t0009g0211a0001c0001t0041g0213others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073+1731G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044773 | ||||||
chr2:206044852
|
G | C | 1 | a0001c0003t0002g0300 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1073+1652C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044852 | ||||||
chr2:206045602
|
C | T | 5 | a0001c0001t0016g0322a0001c0001t0016g0323a0001c0008t0019g0205others(2): Show | 5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073+902G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045602 | ||||||
chr2:206045760
|
A | G | 1 | a0002c0016t0036g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1073+744T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045760 | ||||||
chr2:206045850
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+654C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045850 | ||||||
chr2:206045903
|
T | C | 2 | a0001c0003t0002g0247a0001c0003t0002g0250 | 2 | NA18961.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1073+601A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045903 | ||||||
chr2:206045931
|
G | A | 4 | a0001c0001t0009g0209a0001c0001t0009g0211a0001c0001t0041g0213others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073+573C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045931 | ||||||
chr2:206045983
|
T | C | 5 | a0001c0001t0003g0055a0001c0001t0003g0056a0001c0001t0003g0060others(2): Show | 5 | HG02523.hp1 NA18951.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073+521A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045983 | ||||||
chr2:206046259
|
G | A | 1 | a0002c0005t0040g0326 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1073+245C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206046259 | ||||||
chr2:206046324
|
A | G | 4 | a0001c0001t0009g0209a0001c0001t0009g0211a0001c0001t0041g0213others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073+180T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206046324 | ||||||
chr2:206046343
|
C | T | 1 | a0001c0001t0038g0287 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1073+161G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206046343 | ||||||
chr2:206046467
|
C | CA | 252 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(249): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1073+36dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206046467 | ||||||
chr2:206046782
|
GTTTGTT | G | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.965-176_965-171del others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206046782 | ||||||
chr2:206046787
|
T | C | 4 | a0001c0001t0009g0209a0001c0001t0009g0211a0001c0001t0041g0213others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-175A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206046787 | ||||||
chr2:206046824
|
C | A | 1 | a0001c0004t0011g0219 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.965-212G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206046824 | ||||||
chr2:206047001
|
G | C | 1 | a0001c0003t0002g0267 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.965-389C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047001 | ||||||
chr2:206047165
|
G | A | 1 | a0002c0002t0001g0092 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.965-553C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047165 | ||||||
chr2:206047167
|
G | A | 5 | a0001c0001t0016g0322a0001c0001t0016g0323a0001c0008t0019g0205others(2): Show | 5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-555C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047167 | ||||||
chr2:206047300
|
C | A | 110 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.965-688G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047300 | ||||||
chr2:206047431
|
C | T | 1 | a0002c0002t0001g0129 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.965-819G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047431 | ||||||
chr2:206047432
|
T | C | 1 | a0002c0002t0001g0129 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.965-820A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047432 | ||||||
chr2:206047498
|
C | T | 3 | a0001c0001t0015g0006a0001c0001t0015g0007a0001c0001t0015g0010 | 3 | HG00735.hp2 HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.965-886G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047498 | ||||||
chr2:206047665
|
A | C | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.965-1053T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047665 | ||||||
chr2:206047856
|
A | ATTTTTTT | 88 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(85): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.965-1251_965-1245d others(9): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047856 | ||||||
chr2:206047856
|
A | ATTTTTTT others(1): Show |
10 | a0001c0001t0003g0067a0001c0001t0003g0070a0001c0001t0003g0085others(7): Show | 10 | HG00673.hp2 HG01981.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.965-1252_965-1245d others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047856 | ||||||
chr2:206047856
|
A | ATTTTTTT others(2): Show |
101 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(98): Show | 102 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.965-1253_965-1245d others(11): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047856 | ||||||
chr2:206047856
|
A | ATTTTTTT others(3): Show |
6 | a0002c0002t0001g0132a0002c0002t0001g0147a0002c0002t0001g0168others(3): Show | 6 | HG00140.hp2 HG02145.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.965-1254_965-1245d others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047856 | ||||||
chr2:206047856
|
A | G | 3 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212 | 3 | HG01123.hp2 HG03710.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.965-1244T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047856 | ||||||
chr2:206047937
|
G | A | 9 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(6): Show | 9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-1325C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047937 | ||||||
chr2:206048090
|
T | C | 206 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(203): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.965-1478A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048090 | ||||||
chr2:206048127
|
T | G | 3 | a0002c0005t0002g0327a0002c0005t0006g0328a0002c0005t0040g0326 | 3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.965-1515A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048127 | ||||||
chr2:206048145
|
G | A | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.965-1533C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048145 | ||||||
chr2:206048150
|
C | A | 45 | a0001c0003t0002g0257a0001c0003t0002g0260a0001c0003t0002g0269others(42): Show | 45 | HG00099.hp2 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.965-1538G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048150 | ||||||
chr2:206048154
|
C | T | 2 | a0001c0001t0041g0213a0001c0001t0042g0031 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.965-1542G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048154 | ||||||
chr2:206048423
|
G | A | 1 | a0001c0001t0003g0095 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.965-1811C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048423 | ||||||
chr2:206048438
|
G | A | 1 | a0001c0001t0003g0154 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.965-1826C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048438 | ||||||
chr2:206048452
|
C | T | 1 | a0001c0001t0013g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.965-1840G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048452 | ||||||
chr2:206048624
|
C | T | 2 | a0001c0003t0014g0319a0002c0005t0002g0327 | 2 | HG00438.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.965-2012G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048624 | ||||||
chr2:206049152
|
G | A | 5 | a0001c0001t0015g0006a0001c0001t0015g0007a0001c0001t0015g0010others(2): Show | 5 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-2540C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049152 | ||||||
chr2:206049247
|
G | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-2635C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049247 | ||||||
chr2:206049290
|
G | A | 2 | a0001c0003t0002g0270a0001c0003t0023g0258 | 2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.965-2678C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049290 | ||||||
chr2:206049304
|
T | C | 103 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(100): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.965-2692A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049304 | ||||||
chr2:206049370
|
G | A | 1 | a0002c0002t0001g0092 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.965-2758C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049370 | ||||||
chr2:206049530
|
A | T | 1 | a0002c0002t0001g0131 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.965-2918T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049530 | ||||||
chr2:206049668
|
T | C | 9 | a0001c0001t0003g0047a0001c0001t0003g0068a0001c0001t0003g0069others(6): Show | 9 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-3056A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049668 | ||||||
chr2:206049718
|
C | T | 2 | a0001c0003t0002g0314a0001c0003t0006g0313 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.965-3106G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049718 | ||||||
chr2:206049839
|
T | C | 1 | a0001c0001t0003g0282 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.965-3227A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049839 | ||||||
chr2:206049867
|
C | T | 110 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.965-3255G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049867 | ||||||
chr2:206049992
|
G | T | 1 | a0002c0002t0001g0094 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.965-3380C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049992 | ||||||
chr2:206050095
|
G | A | 3 | a0002c0002t0001g0128a0002c0002t0001g0170a0002c0002t0049g0145 | 3 | HG02145.hp2 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.965-3483C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050095 | ||||||
chr2:206050106
|
C | G | 1 | a0001c0008t0019g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.965-3494G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050106 | ||||||
chr2:206050139
|
A | G | 1 | a0002c0002t0039g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.965-3527T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050139 | ||||||
chr2:206050140
|
G | A | 1 | a0002c0002t0039g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.965-3528C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050140 | ||||||
chr2:206050316
|
C | T | 95 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(92): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.965-3704G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050316 | ||||||
chr2:206050399
|
G | A | 1 | a0001c0001t0013g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.965-3787C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050399 | ||||||
chr2:206050485
|
C | A | 3 | a0001c0001t0009g0209a0001c0001t0009g0210a0001c0001t0009g0211 | 3 | HG02055.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.965-3873G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050485 | ||||||
chr2:206050496
|
G | GA | 20 | a0001c0001t0009g0211a0001c0001t0022g0032a0001c0003t0002g0199others(17): Show | 20 | HG01109.hp2 HG01175.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.965-3885dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | ||||||
chr2:206050496
|
GA | G | 20 | a0001c0001t0002g0230a0001c0001t0005g0087a0001c0001t0005g0088others(17): Show | 20 | HG00423.hp2 HG00558.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.965-3885delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | ||||||
chr2:206050496
|
GAAAAAA | G | 6 | a0002c0002t0001g0129a0002c0002t0001g0166a0002c0005t0002g0327others(3): Show | 6 | HG02109.hp1 HG02165.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.965-3890_965-3885d others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | ||||||
chr2:206050496
|
GAAAAAAA | G | 101 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.965-3891_965-3885d others(9): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | ||||||
chr2:206050496
|
GAAAAAAA others(3): Show |
G | 53 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(50): Show | 54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.965-3894_965-3885d others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | ||||||
chr2:206050496
|
GAAAAAAA others(4): Show |
G | 5 | a0001c0001t0003g0060a0001c0001t0003g0067a0001c0001t0005g0234others(2): Show | 5 | HG02622.hp1 HG02738.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-3895_965-3885d others(13): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | ||||||
chr2:206050496
|
GAAAAAAA others(5): Show |
G | 7 | a0001c0001t0008g0240a0001c0001t0008g0241a0001c0001t0008g0243others(4): Show | 7 | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-3896_965-3885d others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | ||||||
chr2:206050496
|
GAAAAAAA others(6): Show |
G | 23 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(20): Show | 24 | HG00738.hp1 HG01123.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.965-3897_965-3885d others(15): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | ||||||
chr2:206050496
|
GAAAAAAA others(7): Show |
G | 7 | a0001c0001t0015g0006a0001c0001t0015g0007a0001c0001t0015g0010others(4): Show | 7 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-3898_965-3885d others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | ||||||
chr2:206050682
|
T | C | 2 | a0002c0002t0001g0125a0002c0002t0001g0126 | 2 | HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.965-4070A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050682 | ||||||
chr2:206050862
|
G | T | 2 | a0001c0003t0002g0127a0001c0003t0002g0199 | 2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.965-4250C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050862 | ||||||
chr2:206050896
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.965-4284C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050896 | ||||||
chr2:206050924
|
C | G | 240 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(237): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.965-4312G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050924 | ||||||
chr2:206050931
|
T | C | 9 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(6): Show | 9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-4319A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050931 | ||||||
chr2:206050980
|
C | CAAAAATT others(314): Show |
2 | a0001c0004t0007g0202a0001c0004t0007g0212 | 2 | HG03710.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.965-4369_965-4368i others(323): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | ||||||
chr2:206050980
|
C | CAAAAATT others(315): Show |
2 | a0001c0004t0007g0203a0001c0004t0037g0204 | 2 | HG01123.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.965-4369_965-4368i others(324): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | ||||||
chr2:206050980
|
C | CAAAAATT others(321): Show |
2 | a0001c0004t0011g0219a0004c0009t0007g0217 | 2 | HG01257.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.965-4369_965-4368i others(330): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | ||||||
chr2:206050980
|
C | CAAAAATT others(322): Show |
3 | a0001c0004t0007g0216a0001c0004t0011g0214a0004c0009t0011g0215 | 3 | HG00639.hp2 HG01891.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.965-4369_965-4368i others(331): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | ||||||
chr2:206050980
|
C | CAAAAATT others(323): Show |
2 | a0001c0004t0007g0218a0001c0004t0007g0221 | 2 | HG01175.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.965-4369_965-4368i others(332): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | ||||||
chr2:206050980
|
C | CAAAAATT others(324): Show |
1 | a0001c0004t0007g0220 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.965-4369_965-4368i others(333): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | ||||||
chr2:206051215
|
ATTTCT | A | 5 | a0002c0002t0001g0093a0002c0002t0001g0101a0002c0002t0001g0179others(2): Show | 5 | HG01074.hp1 NA18947.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-4608_965-4604d others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051215 | ||||||
chr2:206051219
|
C | T | 5 | a0001c0003t0002g0293a0001c0003t0002g0300a0001c0003t0054g0305others(2): Show | 5 | HG01255.hp1 HG02683.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-4607G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051219 | ||||||
chr2:206051239
|
T | C | 3 | a0002c0005t0002g0327a0002c0005t0006g0328a0002c0005t0040g0326 | 3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.965-4627A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051239 | ||||||
chr2:206051245
|
C | T | 2 | a0001c0001t0005g0232a0001c0001t0005g0233 | 2 | NA18947.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.965-4633G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051245 | ||||||
chr2:206051304
|
G | A | 1 | a0001c0003t0002g0284 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.965-4692C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051304 | ||||||
chr2:206051485
|
A | G | 1 | a0001c0001t0027g0009 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.964+4713T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051485 | ||||||
chr2:206051562
|
T | C | 1 | a0001c0004t0037g0204 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.964+4636A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051562 | ||||||
chr2:206051671
|
A | T | 1 | a0002c0002t0039g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.964+4527T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051671 | ||||||
chr2:206051701
|
A | G | 1 | a0001c0001t0003g0081 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.964+4497T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051701 | ||||||
chr2:206051715
|
G | A | 2 | a0002c0002t0001g0125a0002c0002t0001g0126 | 2 | HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.964+4483C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051715 | ||||||
chr2:206051999
|
A | C | 1 | a0003c0007t0001g0163 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.964+4199T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051999 | ||||||
chr2:206052058
|
T | G | 1 | a0001c0003t0059g0275 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.964+4140A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052058 | ||||||
chr2:206052154
|
T | C | 1 | a0002c0002t0001g0162 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.964+4044A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052154 | ||||||
chr2:206052257
|
G | A | 111 | a0001c0001t0031g0246a0001c0006t0001g0110a0001c0006t0001g0122others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.964+3941C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052257 | ||||||
chr2:206052293
|
A | G | 1 | a0001c0003t0002g0127 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.964+3905T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052293 | ||||||
chr2:206052661
|
G | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+3537C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052661 | ||||||
chr2:206052732
|
C | T | 1 | a0001c0001t0004g0021 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.964+3466G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052732 | ||||||
chr2:206052791
|
C | CA | 84 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(81): Show | 86 | HG00323.hp2 HG00673.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.964+3406dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052791 | ||||||
chr2:206052791
|
C | CAA | 9 | a0001c0001t0003g0047a0001c0001t0003g0068a0001c0001t0003g0069others(6): Show | 9 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.964+3405_964+3406d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052791 | ||||||
chr2:206052953
|
A | C | 2 | a0001c0001t0008g0243a0001c0001t0050g0239 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.964+3245T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052953 | ||||||
chr2:206053004
|
C | A | 205 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(202): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.964+3194G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053004 | ||||||
chr2:206053380
|
T | C | 110 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.964+2818A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053380 | ||||||
chr2:206053456
|
G | A | 95 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(92): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.964+2742C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053456 | ||||||
chr2:206053513
|
C | T | 59 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(56): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.964+2685G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053513 | ||||||
chr2:206053593
|
T | C | 1 | a0002c0002t0001g0141 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.964+2605A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053593 | ||||||
chr2:206053842
|
A | AT | 108 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(105): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.964+2355dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053842 | ||||||
chr2:206053869
|
C | T | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+2329G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053869 | ||||||
chr2:206054012
|
G | A | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.964+2186C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054012 | ||||||
chr2:206054041
|
T | C | 2 | a0001c0003t0006g0291a0001c0003t0006g0296 | 2 | HG00673.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.964+2157A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054041 | ||||||
chr2:206054188
|
T | C | 1 | a0001c0001t0008g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.964+2010A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054188 | ||||||
chr2:206054583
|
G | A | 2 | a0001c0001t0003g0050a0001c0001t0003g0059 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.964+1615C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054583 | ||||||
chr2:206054607
|
AG | A | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.964+1590delC | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054607 | ||||||
chr2:206054784
|
G | C | 1 | a0001c0003t0062g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.964+1414C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054784 | ||||||
chr2:206055372
|
G | A | 1 | a0001c0004t0007g0216 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.964+826C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055372 | ||||||
chr2:206055435
|
G | A | 1 | a0002c0002t0001g0201 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.964+763C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055435 | ||||||
chr2:206055469
|
T | C | 10 | a0002c0002t0001g0091a0002c0002t0001g0104a0002c0002t0001g0114others(7): Show | 10 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.964+729A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055469 | ||||||
chr2:206055628
|
G | A | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.964+570C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055628 | ||||||
chr2:206055643
|
C | T | 1 | a0001c0003t0002g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.964+555G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055643 | ||||||
chr2:206055692
|
G | A | 1 | a0002c0002t0001g0161 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.964+506C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055692 | ||||||
chr2:206055875
|
G | A | 59 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(56): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.964+323C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055875 | ||||||
chr2:206056111
|
T | C | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.964+87A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206056111 | ||||||
chr2:206056145
|
G | A | 2 | a0001c0003t0002g0315a0001c0003t0006g0312 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.964+53C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206056145 | ||||||
chr2:206056169
|
T | C | 1 | a0001c0003t0002g0284 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964+29A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206056169 | ||||||
chr2:206057039
|
C | T | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.219-96G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057039 | ||||||
chr2:206057413
|
C | T | 2 | a0002c0002t0001g0106a0002c0002t0001g0194 | 2 | HG00621.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.219-470G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057413 | ||||||
chr2:206057421
|
C | G | 1 | a0002c0016t0036g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.219-478G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057421 | ||||||
chr2:206057485
|
T | C | 1 | a0001c0001t0003g0073 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.219-542A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057485 | ||||||
chr2:206057665
|
A | G | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.219-722T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057665 | ||||||
chr2:206057778
|
G | A | 316 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(313): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.219-835C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057778 | ||||||
chr2:206057899
|
TA | T | 11 | a0001c0001t0003g0049a0001c0001t0005g0235a0001c0001t0008g0243others(8): Show | 11 | HG00323.hp2 HG00558.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.219-957delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057899 | ||||||
chr2:206057939
|
T | G | 1 | a0001c0001t0013g0207 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.219-996A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057939 | ||||||
chr2:206058149
|
A | G | 213 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(210): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.219-1206T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058149 | ||||||
chr2:206058150
|
A | G | 213 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(210): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.219-1207T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058150 | ||||||
chr2:206058194
|
C | T | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219-1251G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058194 | ||||||
chr2:206058311
|
C | T | 3 | a0001c0004t0007g0216a0001c0004t0007g0218a0001c0004t0007g0220 | 3 | HG00639.hp2 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.219-1368G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058311 | ||||||
chr2:206058329
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219-1386C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058329 | ||||||
chr2:206058368
|
G | A | 5 | a0001c0001t0015g0006a0001c0001t0015g0007a0001c0001t0015g0010others(2): Show | 5 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-1425C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058368 | ||||||
chr2:206058381
|
T | G | 1 | a0002c0002t0001g0195 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.219-1438A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058381 | ||||||
chr2:206058418
|
C | CA | 56 | a0001c0001t0002g0208a0001c0001t0005g0089a0001c0001t0005g0224others(53): Show | 56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.219-1476dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058418 | ||||||
chr2:206058418
|
C | CAA | 11 | a0001c0001t0002g0230a0001c0001t0005g0087a0001c0001t0005g0088others(8): Show | 11 | HG02055.hp1 HG02135.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.219-1477_219-1476d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058418 | ||||||
chr2:206058418
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0003g0079a0001c0001t0029g0063a0002c0005t0002g0327others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-1486_219-1476d others(13): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058418 | ||||||
chr2:206058418
|
CAAAAAAA others(5): Show |
C | 208 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(205): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.219-1487_219-1476d others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058418 | ||||||
chr2:206058507
|
G | C | 17 | a0001c0003t0002g0127a0001c0003t0002g0160a0001c0003t0002g0171others(14): Show | 17 | HG00438.hp1 HG02071.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-1564C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058507 | ||||||
chr2:206058660
|
G | A | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.219-1717C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058660 | ||||||
chr2:206058861
|
T | G | 1 | a0001c0001t0025g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.219-1918A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058861 | ||||||
chr2:206059062
|
TA | T | 14 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(11): Show | 14 | HG00323.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-2120delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206059062 | ||||||
chr2:206059237
|
C | T | 1 | a0001c0004t0007g0221 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.219-2294G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206059237 | ||||||
chr2:206059303
|
C | T | 1 | a0002c0002t0001g0129 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.219-2360G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206059303 | ||||||
chr2:206059363
|
AG | A | 19 | a0001c0003t0002g0127a0001c0003t0002g0160a0001c0003t0002g0171others(16): Show | 19 | HG00438.hp1 HG02071.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.219-2421delC | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206059363 | ||||||
chr2:206059740
|
C | CGT | 9 | a0001c0001t0003g0047a0001c0001t0003g0068a0001c0001t0003g0069others(6): Show | 9 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-2799_219-2798d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206059740 | ||||||
chr2:206060017
|
A | C | 1 | a0001c0003t0002g0286 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.218+2782T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060017 | ||||||
chr2:206060056
|
C | T | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.218+2743G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060056 | ||||||
chr2:206060155
|
C | T | 25 | a0001c0001t0003g0002a0001c0001t0003g0048a0001c0001t0003g0051others(22): Show | 26 | HG00673.hp2 HG02132.hp1 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.218+2644G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060155 | ||||||
chr2:206060156
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.218+2643C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060156 | ||||||
chr2:206060313
|
A | C | 2 | a0002c0002t0001g0103a0002c0002t0001g0195 | 2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.218+2486T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060313 | ||||||
chr2:206060394
|
G | A | 4 | a0002c0002t0001g0097a0002c0002t0001g0142a0002c0002t0001g0153others(1): Show | 4 | HG01081.hp2 HG03834.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+2405C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060394 | ||||||
chr2:206060472
|
C | T | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.218+2327G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060472 | ||||||
chr2:206060532
|
CA | C | 116 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(113): Show | 116 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.218+2266delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060532 | ||||||
chr2:206060542
|
A | C | 9 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(6): Show | 9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.218+2257T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060542 | ||||||
chr2:206060564
|
C | CT | 101 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(98): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.218+2234dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060564 | ||||||
chr2:206060582
|
C | T | 10 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(7): Show | 10 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.218+2217G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060582 | ||||||
chr2:206060588
|
T | C | 3 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188 | 3 | NA18951.hp2 NA18977.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.218+2211A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060588 | ||||||
chr2:206060621
|
C | T | 1 | a0003c0007t0045g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.218+2178G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060621 | ||||||
chr2:206060646
|
C | T | 1 | a0001c0003t0002g0318 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.218+2153G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060646 | ||||||
chr2:206060752
|
G | T | 2 | a0001c0003t0014g0248a0001c0003t0014g0251 | 2 | NA18945.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.218+2047C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060752 | ||||||
chr2:206060825
|
G | T | 3 | a0001c0001t0009g0209a0001c0001t0009g0210a0001c0001t0009g0211 | 3 | HG02055.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.218+1974C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060825 | ||||||
chr2:206061021
|
C | CT | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+1777dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061021 | ||||||
chr2:206061030
|
T | A | 115 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(112): Show | 115 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.218+1769A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061030 | ||||||
chr2:206061051
|
T | C | 1 | a0002c0002t0001g0197 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.218+1748A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061051 | ||||||
chr2:206061138
|
A | G | 90 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(87): Show | 92 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.218+1661T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061138 | ||||||
chr2:206061223
|
G | C | 1 | a0001c0001t0004g0021 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.218+1576C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061223 | ||||||
chr2:206061234
|
ACTC | A | 25 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.218+1562_218+1564d others(5): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061234 | ||||||
chr2:206062075
|
A | G | 1 | a0001c0001t0038g0287 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.218+724T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062075 | ||||||
chr2:206062105
|
G | C | 1 | a0002c0002t0001g0105 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.218+694C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062105 | ||||||
chr2:206062186
|
A | G | 11 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(8): Show | 11 | HG02451.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+613T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062186 | ||||||
chr2:206062316
|
T | C | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.218+483A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062316 | ||||||
chr2:206062495
|
T | C | 1 | a0002c0002t0001g0162 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.218+304A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062495 | ||||||
chr2:206062633
|
T | C | 1 | a0002c0016t0036g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.218+166A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062633 | ||||||
chr2:206062671
|
T | C | 2 | a0001c0001t0003g0069a0001c0001t0003g0071 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.218+128A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062671 | ||||||
chr2:206062711
|
CAGAAGAA others(3): Show |
C | 3 | a0002c0005t0002g0327a0002c0005t0006g0328a0002c0005t0040g0326 | 3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.218+78_218+87delCT others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062711 | ||||||
chr2:206063091
|
A | C | 1 | a0001c0001t0013g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-29-46T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 2/10 | chr2 | 206063091 | ||||||
chr2:206063126
|
G | A | 86 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(83): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-30+25C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 2/10 | chr2 | 206063126 | ||||||
chr2:206063429
|
C | T | 1 | a0001c0003t0002g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-123-185G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063429 | ||||||
chr2:206063438
|
C | T | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-123-194G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063438 | ||||||
chr2:206063439
|
G | A | 9 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(6): Show | 9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-123-195C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063439 | ||||||
chr2:206063452
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-208C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063452 | ||||||
chr2:206063528
|
T | C | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-284A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063528 | ||||||
chr2:206063544
|
C | A | 222 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(219): Show | 224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-123-300G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063544 | ||||||
chr2:206063668
|
T | C | 4 | a0001c0003t0002g0294a0001c0003t0002g0302a0001c0003t0002g0304others(1): Show | 4 | HG01361.hp1 HG01515.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-123-424A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063668 | ||||||
chr2:206063856
|
T | C | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-612A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063856 | ||||||
chr2:206063892
|
A | G | 1 | a0001c0001t0003g0049 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-123-648T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063892 | ||||||
chr2:206064078
|
A | G | 78 | a0001c0003t0002g0127a0001c0003t0002g0160a0001c0003t0002g0171others(75): Show | 78 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.-123-834T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206064078 | ||||||
chr2:206064446
|
T | C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-1202A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206064446 | ||||||
chr2:206064817
|
GA | G | 86 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(83): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-123-1574delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206064817 | ||||||
chr2:206064878
|
GA | G | 45 | a0001c0003t0002g0257a0001c0003t0002g0260a0001c0003t0002g0269others(42): Show | 45 | HG00099.hp2 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.-123-1635delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206064878 | ||||||
chr2:206065220
|
CAGCACTT others(5243): Show |
C | 1 | a0001c0001t0018g0008 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-123-7226_-123-197 others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065220 | ||||||
chr2:206065267
|
G | A | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-123-2023C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065267 | ||||||
chr2:206065426
|
G | A | 2 | a0001c0001t0004g0022a0001c0001t0024g0013 | 2 | HG01978.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-123-2182C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065426 | ||||||
chr2:206065536
|
T | A | 1 | a0001c0001t0022g0032 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-123-2292A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065536 | ||||||
chr2:206065974
|
C | T | 322 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(319): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-123-2730G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065974 | ||||||
chr2:206065998
|
G | A | 117 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(114): Show | 117 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-123-2754C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065998 | ||||||
chr2:206066048
|
T | G | 3 | a0001c0004t0007g0216a0001c0004t0007g0218a0001c0004t0007g0220 | 3 | HG00639.hp2 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-123-2804A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066048 | ||||||
chr2:206066093
|
C | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(23): Show | 27 | HG00735.hp2 HG00738.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-123-2849G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066093 | ||||||
chr2:206066132
|
C | T | 2 | a0001c0001t0003g0072a0001c0001t0003g0078 | 2 | HG00140.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-123-2888G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066132 | ||||||
chr2:206066154
|
A | G | 219 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(216): Show | 221 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-123-2910T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066154 | ||||||
chr2:206066207
|
G | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-123-2963C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066207 | ||||||
chr2:206066250
|
T | C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-3006A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066250 | ||||||
chr2:206066322
|
C | T | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-123-3078G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066322 | ||||||
chr2:206066534
|
G | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(23): Show | 27 | HG00735.hp2 HG00738.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-123-3290C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066534 | ||||||
chr2:206066760
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-3516C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066760 | ||||||
chr2:206066804
|
C | CA | 106 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(103): Show | 108 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-123-3561dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066804 | ||||||
chr2:206066804
|
CA | C | 9 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(6): Show | 9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-123-3561delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066804 | ||||||
chr2:206066949
|
CAT | C | 101 | a0001c0001t0002g0033a0001c0001t0003g0002a0001c0001t0003g0039others(98): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-123-3707_-123-370 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066949 | ||||||
chr2:206067030
|
T | A | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-123-3786A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067030 | ||||||
chr2:206067093
|
C | CA | 219 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(216): Show | 221 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-123-3850dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067093 | ||||||
chr2:206067219
|
C | T | 1 | a0002c0002t0001g0094 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-123-3975G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067219 | ||||||
chr2:206067312
|
T | C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-4068A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067312 | ||||||
chr2:206067451
|
G | A | 12 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212others(9): Show | 12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-123-4207C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067451 | ||||||
chr2:206067597
|
TA | T | 86 | a0001c0006t0001g0110a0001c0006t0001g0122a0001c0006t0001g0188others(83): Show | 87 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-123-4354delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067597 | ||||||
chr2:206067716
|
T | G | 222 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(219): Show | 224 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.-123-4472A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067716 | ||||||
chr2:206067756
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0054a0001c0001t0003g0074 | 4 | NA18977.hp2 NA18983.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.-123-4512G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067756 | ||||||
chr2:206067759
|
A | G | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-123-4515T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067759 | ||||||
chr2:206068040
|
T | C | 2 | a0002c0002t0001g0096a0002c0002t0001g0144 | 2 | HG00423.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-123-4796A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068040 | ||||||
chr2:206068132
|
C | T | 5 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(2): Show | 5 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-123-4888G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068132 | ||||||
chr2:206068200
|
A | G | 162 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(159): Show | 163 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.-123-4956T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068200 | ||||||
chr2:206068291
|
G | C | 3 | a0001c0001t0009g0222a0001c0001t0009g0223a0001c0001t0009g0329 | 3 | HG02145.hp1 HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-123-5047C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068291 | ||||||
chr2:206068506
|
C | T | 1 | a0002c0002t0001g0126 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-123-5262G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068506 | ||||||
chr2:206068795
|
G | A | 1 | a0002c0002t0001g0093 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-123-5551C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068795 | ||||||
chr2:206069266
|
A | G | 1 | a0002c0010t0055g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-123-6022T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206069266 | ||||||
chr2:206069463
|
T | C | 1 | a0001c0003t0002g0297 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-123-6219A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206069463 | ||||||
chr2:206069731
|
C | T | 3 | a0001c0001t0031g0246a0001c0001t0041g0213a0001c0001t0042g0031 | 3 | HG02970.hp2 HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-123-6487G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206069731 | ||||||
chr2:206070006
|
G | A | 80 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(77): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.-123-6762C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070006 | ||||||
chr2:206070007
|
T | A | 1 | a0001c0003t0006g0321 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-123-6763A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070007 | ||||||
chr2:206070009
|
C | A | 1 | a0001c0003t0006g0321 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-123-6765G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070009 | ||||||
chr2:206070010
|
A | T | 1 | a0001c0003t0006g0321 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-123-6766T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070010 | ||||||
chr2:206070014
|
C | G | 1 | a0001c0003t0006g0321 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-123-6770G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070014 | ||||||
chr2:206070022
|
C | T | 1 | a0001c0003t0006g0321 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-123-6778G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070022 | ||||||
chr2:206070177
|
G | A | 25 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-123-6933C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070177 | ||||||
chr2:206070449
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-7205C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070449 | ||||||
chr2:206070470
|
T | C | 213 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(210): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.-123-7226A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070470 | ||||||
chr2:206070775
|
G | T | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-7531C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070775 | ||||||
chr2:206070880
|
G | A | 87 | a0001c0001t0003g0282a0001c0003t0002g0247a0001c0003t0002g0249others(84): Show | 87 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.-123-7636C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070880 | ||||||
chr2:206070889
|
A | AT | 98 | a0001c0001t0002g0033a0001c0001t0002g0230a0001c0001t0003g0282others(95): Show | 99 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.-123-7646dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070889 | ||||||
chr2:206070889
|
A | ATT | 12 | a0001c0001t0009g0223a0001c0001t0009g0329a0001c0001t0013g0030others(9): Show | 12 | HG01978.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-123-7647_-123-764 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070889 | ||||||
chr2:206070889
|
AT | A | 14 | a0001c0001t0005g0224a0001c0004t0007g0202a0001c0004t0007g0203others(11): Show | 14 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-123-7646delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070889 | ||||||
chr2:206070889
|
ATTT | A | 51 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(48): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.-123-7648_-123-764 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070889 | ||||||
chr2:206071011
|
G | A | 2 | a0001c0001t0041g0213a0001c0001t0042g0031 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-123-7767C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071011 | ||||||
chr2:206071243
|
G | GC | 330 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-123-8000dupG | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071243 | ||||||
chr2:206071254
|
G | A | 2 | a0001c0001t0012g0084a0001c0001t0012g0086 | 2 | NA18971.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-123-8010C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071254 | ||||||
chr2:206071257
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0012g0086a0002c0002t0001g0185a0002c0002t0010g0109others(2): Show | 5 | HG03239.hp2 HG04199.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.-123-8023_-123-801 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(4): Show |
C | 5 | a0002c0002t0001g0091a0002c0002t0001g0094a0002c0002t0001g0106others(2): Show | 5 | HG01069.hp2 HG01168.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123-8024_-123-801 others(15): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(5): Show |
C | 4 | a0002c0002t0001g0092a0002c0002t0001g0103a0002c0002t0001g0196others(1): Show | 4 | HG00140.hp2 HG01346.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123-8025_-123-801 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0012g0084a0002c0002t0001g0105a0002c0002t0035g0118others(2): Show | 5 | HG02698.hp2 HG03654.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123-8026_-123-801 others(17): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0003g0051a0001c0001t0012g0080a0001c0001t0022g0034others(2): Show | 5 | HG01074.hp1 HG03579.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-123-8027_-123-801 others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(8): Show |
C | 6 | a0001c0006t0001g0110a0001c0006t0001g0122a0002c0002t0001g0121others(3): Show | 6 | HG00738.hp2 NA18944.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.-123-8028_-123-801 others(19): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(9): Show |
C | 9 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0003t0002g0199others(6): Show | 9 | HG01071.hp2 HG01081.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.-123-8029_-123-801 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(10): Show |
C | 46 | a0001c0001t0003g0048a0001c0001t0021g0046a0001c0001t0021g0053others(43): Show | 47 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-123-8030_-123-801 others(21): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(11): Show |
C | 33 | a0001c0001t0003g0050a0001c0001t0003g0054a0001c0001t0003g0055others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.-123-8031_-123-801 others(22): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(12): Show |
C | 19 | a0001c0001t0003g0002a0001c0001t0003g0040a0001c0001t0003g0041others(16): Show | 20 | HG00741.hp2 HG01099.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-123-8032_-123-801 others(23): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(13): Show |
C | 12 | a0001c0001t0003g0039a0001c0001t0003g0042a0001c0001t0003g0047others(9): Show | 12 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.-123-8033_-123-801 others(24): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(14): Show |
C | 4 | a0001c0001t0013g0030a0002c0002t0001g0156a0002c0002t0001g0183others(1): Show | 4 | HG00735.hp1 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123-8034_-123-801 others(25): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0002g0033a0002c0002t0001g0184 | 2 | HG00280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-123-8035_-123-801 others(26): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0013g0207 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-123-8036_-123-801 others(27): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(17): Show |
C | 2 | a0001c0001t0016g0322a0001c0001t0016g0323 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-8037_-123-801 others(28): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(18): Show |
C | 3 | a0002c0002t0001g0098a0002c0002t0001g0193a0002c0002t0001g0198 | 3 | HG02559.hp1 HG02735.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-123-8038_-123-801 others(29): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(22): Show |
C | 2 | a0002c0002t0001g0175a0002c0002t0001g0186 | 2 | HG00438.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-123-8042_-123-801 others(33): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(23): Show |
C | 1 | a0002c0002t0001g0201 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-123-8043_-123-801 others(34): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(25): Show |
C | 8 | a0001c0001t0041g0213a0001c0001t0042g0031a0001c0003t0002g0250others(5): Show | 8 | HG02486.hp2 HG02970.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.-123-8045_-123-801 others(36): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(26): Show |
C | 17 | a0001c0001t0008g0238a0001c0001t0030g0062a0001c0003t0002g0247others(14): Show | 17 | HG00673.hp1 HG01106.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.-123-8046_-123-801 others(37): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(27): Show |
C | 66 | a0001c0001t0003g0282a0001c0001t0008g0240a0001c0001t0008g0241others(63): Show | 66 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-123-8047_-123-801 others(38): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(28): Show |
C | 5 | a0001c0001t0004g0026a0001c0003t0002g0302a0001c0003t0017g0307others(2): Show | 5 | HG01891.hp2 HG02148.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123-8048_-123-801 others(39): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(29): Show |
C | 35 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(32): Show | 36 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-123-8049_-123-801 others(40): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(30): Show |
C | 3 | a0001c0001t0027g0009a0002c0002t0001g0166a0002c0016t0036g0112 | 3 | HG01256.hp2 HG02165.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-123-8050_-123-801 others(41): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(33): Show |
C | 25 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-123-8053_-123-801 others(44): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(35): Show |
C | 1 | a0002c0002t0001g0157 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-123-8055_-123-801 others(46): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(37): Show |
C | 1 | a0002c0002t0001g0097 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-123-8057_-123-801 others(48): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071257
|
CTTTTTTT others(38): Show |
C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-8058_-123-801 others(49): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | ||||||
chr2:206071746
|
C | T | 2 | a0001c0001t0041g0213a0001c0001t0042g0031 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-123-8502G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071746 | ||||||
chr2:206071820
|
C | T | 1 | a0001c0001t0022g0032 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-123-8576G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071820 | ||||||
chr2:206072270
|
G | A | 2 | a0001c0003t0002g0302a0001c0003t0002g0304 | 2 | HG01361.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-123-9026C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072270 | ||||||
chr2:206072285
|
G | GT | 27 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0003g0090others(24): Show | 27 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.-123-9042dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072285 | ||||||
chr2:206072364
|
C | T | 25 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-123-9120G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072364 | ||||||
chr2:206072533
|
C | T | 2 | a0001c0003t0002g0277a0001c0003t0007g0281 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-123-9289G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072533 | ||||||
chr2:206072570
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-9326C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072570 | ||||||
chr2:206072763
|
C | T | 2 | a0002c0002t0010g0244a0002c0002t0046g0245 | 2 | NA18989.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-123-9519G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072763 | ||||||
chr2:206072846
|
C | CTT | 84 | a0001c0001t0003g0282a0001c0003t0002g0160a0001c0003t0002g0249others(81): Show | 84 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.-123-9604_-123-960 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072846 | ||||||
chr2:206072846
|
CT | C | 21 | a0001c0001t0002g0033a0001c0001t0003g0039a0001c0001t0003g0049others(18): Show | 21 | HG00323.hp2 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-123-9603delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072846 | ||||||
chr2:206072896
|
G | A | 3 | a0002c0005t0002g0327a0002c0005t0006g0328a0002c0005t0040g0326 | 3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-123-9652C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072896 | ||||||
chr2:206073454
|
A | G | 1 | a0002c0002t0001g0193 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-123-10210T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073454 | ||||||
chr2:206073481
|
T | A | 84 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(81): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-123-10237A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073481 | ||||||
chr2:206073551
|
G | T | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-10307C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073551 | ||||||
chr2:206073799
|
G | A | 2 | a0001c0003t0002g0280a0001c0003t0002g0283 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-123-10555C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073799 | ||||||
chr2:206073915
|
T | C | 1 | a0002c0002t0001g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-123-10671A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073915 | ||||||
chr2:206073984
|
C | T | 25 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-123-10740G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073984 | ||||||
chr2:206074033
|
G | A | 1 | a0001c0001t0002g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-123-10789C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074033 | ||||||
chr2:206074061
|
C | A | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-10817G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074061 | ||||||
chr2:206074115
|
AGAC | A | 3 | a0001c0004t0007g0216a0001c0004t0007g0218a0001c0004t0007g0220 | 3 | HG00639.hp2 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-123-10874_-123-10 others(9): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074115 | ||||||
chr2:206074183
|
C | T | 3 | a0001c0001t0016g0322a0001c0001t0016g0323a0005c0015t0016g0324 | 3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-10939G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074183 | ||||||
chr2:206074271
|
C | T | 25 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-123-11027G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074271 | ||||||
chr2:206074278
|
A | C | 1 | a0002c0016t0036g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-123-11034T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074278 | ||||||
chr2:206074352
|
G | A | 1 | a0001c0001t0002g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-123-11108C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074352 | ||||||
chr2:206074563
|
G | A | 1 | a0003c0007t0045g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-123-11319C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074563 | ||||||
chr2:206074671
|
G | A | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-124+11230C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074671 | ||||||
chr2:206074726
|
G | A | 2 | a0001c0001t0041g0213a0001c0001t0042g0031 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-124+11175C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074726 | ||||||
chr2:206075039
|
C | CAAAAA | 98 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0003g0002others(95): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.-124+10857_-124+10 others(11): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAA | 16 | a0001c0001t0003g0039a0001c0001t0003g0067a0001c0001t0005g0087others(13): Show | 16 | HG00558.hp1 HG00642.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.-124+10856_-124+10 others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA | 67 | a0001c0001t0003g0282a0001c0001t0005g0229a0001c0001t0005g0231others(64): Show | 67 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.-124+10855_-124+10 others(13): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(1): Show |
7 | a0001c0003t0002g0277a0001c0003t0002g0289a0001c0003t0006g0255others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+10854_-124+10 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(3): Show |
1 | a0001c0004t0037g0204 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-124+10852_-124+10 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0013g0036a0001c0001t0041g0213a0001c0001t0042g0031 | 3 | HG02970.hp2 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-124+10850_-124+10 others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(6): Show |
7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+10849_-124+10 others(19): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0013g0207 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-124+10848_-124+10 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+10861_-124+10 others(27): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(16): Show |
2 | a0004c0009t0007g0217a0004c0009t0011g0215 | 2 | HG01257.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-124+10861_-124+10 others(29): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(17): Show |
2 | a0001c0004t0007g0216a0001c0004t0007g0218 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-124+10861_-124+10 others(30): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(19): Show |
1 | a0001c0004t0011g0214 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-124+10861_-124+10 others(32): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(22): Show |
2 | a0001c0004t0007g0202a0001c0004t0007g0212 | 2 | HG03710.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-124+10861_-124+10 others(35): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(24): Show |
1 | a0001c0004t0007g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-124+10861_-124+10 others(37): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075039
|
C | CAAAAAAA others(25): Show |
2 | a0001c0004t0007g0220a0001c0004t0011g0219 | 2 | HG01243.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-124+10861_-124+10 others(38): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | ||||||
chr2:206075094
|
T | C | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+10807A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075094 | ||||||
chr2:206075438
|
A | AT | 79 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(76): Show | 81 | HG00323.hp2 HG00673.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.-124+10462dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075438 | ||||||
chr2:206075438
|
AT | A | 6 | a0001c0003t0002g0267a0002c0002t0001g0161a0002c0002t0001g0162others(3): Show | 6 | HG00558.hp2 HG00639.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+10462delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075438 | ||||||
chr2:206075499
|
C | T | 9 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(6): Show | 9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-124+10402G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075499 | ||||||
chr2:206075505
|
T | G | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+10396A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075505 | ||||||
chr2:206075524
|
C | T | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+10377G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075524 | ||||||
chr2:206075547
|
C | T | 1 | a0002c0002t0001g0166 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-124+10354G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075547 | ||||||
chr2:206075626
|
G | A | 1 | a0002c0005t0040g0326 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-124+10275C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075626 | ||||||
chr2:206075690
|
G | A | 1 | a0002c0005t0040g0326 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-124+10211C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075690 | ||||||
chr2:206075829
|
G | A | 1 | a0001c0001t0022g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-124+10072C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075829 | ||||||
chr2:206076051
|
C | CA | 6 | a0001c0001t0002g0230a0001c0001t0005g0088a0001c0001t0009g0223others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+9849dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076051 | ||||||
chr2:206076051
|
CA | C | 67 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(64): Show | 68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-124+9849delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076051 | ||||||
chr2:206076051
|
CAA | C | 29 | a0001c0001t0003g0050a0001c0001t0004g0001a0001c0001t0004g0011others(26): Show | 30 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-124+9848_-124+984 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076051 | ||||||
chr2:206076114
|
G | A | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-124+9787C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076114 | ||||||
chr2:206076155
|
T | C | 1 | a0001c0001t0022g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-124+9746A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076155 | ||||||
chr2:206076298
|
G | A | 9 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(6): Show | 9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-124+9603C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076298 | ||||||
chr2:206076498
|
A | T | 1 | a0001c0003t0002g0260 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-124+9403T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076498 | ||||||
chr2:206076646
|
C | T | 1 | a0001c0006t0001g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-124+9255G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076646 | ||||||
chr2:206076856
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.-124+9045C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076856 | ||||||
chr2:206076937
|
T | G | 1 | a0001c0001t0008g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-124+8964A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076937 | ||||||
chr2:206076961
|
T | C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+8940A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076961 | ||||||
chr2:206076977
|
T | C | 91 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(88): Show | 93 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.-124+8924A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076977 | ||||||
chr2:206077056
|
G | A | 87 | a0001c0001t0003g0282a0001c0003t0002g0247a0001c0003t0002g0249others(84): Show | 87 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.-124+8845C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077056 | ||||||
chr2:206077072
|
G | A | 1 | a0001c0003t0002g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-124+8829C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077072 | ||||||
chr2:206077253
|
T | C | 25 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-124+8648A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077253 | ||||||
chr2:206077262
|
C | T | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-124+8639G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077262 | ||||||
chr2:206077308
|
C | T | 1 | a0002c0002t0010g0109 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-124+8593G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077308 | ||||||
chr2:206077334
|
T | C | 1 | a0001c0003t0014g0319 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-124+8567A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077334 | ||||||
chr2:206077339
|
C | CA | 29 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0282others(26): Show | 29 | HG00438.hp1 HG01981.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.-124+8561dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077339 | ||||||
chr2:206077353
|
C | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+8548G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077353 | ||||||
chr2:206077801
|
G | A | 1 | a0002c0002t0056g0177 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-124+8100C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077801 | ||||||
chr2:206078061
|
C | CA | 56 | a0001c0001t0002g0033a0001c0001t0004g0001a0001c0001t0004g0011others(53): Show | 57 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.-124+7839dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
C | CAA | 11 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0073others(8): Show | 11 | HG00323.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-124+7838_-124+783 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
C | CAAA | 39 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0041others(36): Show | 40 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.-124+7837_-124+783 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
C | CAAAA | 13 | a0001c0001t0003g0040a0001c0001t0003g0042a0001c0001t0003g0068others(10): Show | 13 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.-124+7836_-124+783 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
C | CAAAAAA | 8 | a0001c0003t0061g0256a0001c0004t0007g0202a0001c0004t0007g0212others(5): Show | 8 | HG01175.hp1 HG01243.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-124+7834_-124+783 others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
C | CAAAAAAA | 8 | a0001c0003t0002g0269a0001c0003t0002g0270a0001c0003t0002g0271others(5): Show | 8 | HG01891.hp2 HG02135.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-124+7833_-124+783 others(11): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
C | CAAAAAAA others(1): Show |
20 | a0001c0003t0002g0257a0001c0003t0002g0260a0001c0003t0002g0273others(17): Show | 20 | HG00621.hp2 HG01070.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-124+7832_-124+783 others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
C | CAAAAAAA others(2): Show |
27 | a0001c0001t0003g0282a0001c0003t0002g0247a0001c0003t0002g0249others(24): Show | 27 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.-124+7831_-124+783 others(13): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
C | CAAAAAAA others(3): Show |
14 | a0001c0003t0002g0250a0001c0003t0002g0265a0001c0003t0002g0266others(11): Show | 14 | HG01884.hp1 HG01981.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-124+7830_-124+783 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
C | CAAAAAAA others(4): Show |
5 | a0001c0003t0002g0302a0001c0003t0002g0315a0001c0003t0006g0313others(2): Show | 5 | HG03098.hp2 HG03654.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-124+7829_-124+783 others(15): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
C | CAAAAAAA others(5): Show |
1 | a0001c0003t0002g0314 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-124+7828_-124+783 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
CA | C | 9 | a0001c0001t0005g0089a0001c0001t0005g0231a0001c0001t0009g0223others(6): Show | 9 | HG00423.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-124+7839delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
CAA | C | 18 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(15): Show | 18 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-124+7838_-124+783 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0016g0322a0001c0001t0016g0323 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-124+7830_-124+783 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078061
|
CAAAAAAA others(8): Show |
C | 1 | a0002c0017t0052g0099 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-124+7825_-124+783 others(19): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | ||||||
chr2:206078211
|
A | G | 1 | a0002c0002t0001g0107 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-124+7690T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078211 | ||||||
chr2:206078275
|
G | A | 1 | a0002c0002t0001g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-124+7626C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078275 | ||||||
chr2:206078290
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+7611C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078290 | ||||||
chr2:206078341
|
G | A | 4 | a0002c0002t0001g0101a0002c0002t0001g0179a0002c0002t0001g0187others(1): Show | 4 | NA18947.hp2 NA18964.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-124+7560C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078341 | ||||||
chr2:206078520
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-124+7381C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078520 | ||||||
chr2:206078521
|
G | A | 1 | a0001c0001t0003g0044 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-124+7380C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078521 | ||||||
chr2:206078648
|
CA | C | 88 | a0001c0001t0003g0282a0001c0003t0002g0247a0001c0003t0002g0249others(85): Show | 88 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-124+7252delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078648 | ||||||
chr2:206078685
|
G | A | 88 | a0001c0001t0003g0282a0001c0003t0002g0247a0001c0003t0002g0249others(85): Show | 88 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-124+7216C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078685 | ||||||
chr2:206078874
|
C | T | 2 | a0001c0001t0003g0047a0001c0001t0003g0076 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-124+7027G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078874 | ||||||
chr2:206078895
|
C | G | 1 | a0001c0003t0014g0319 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-124+7006G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078895 | ||||||
chr2:206078898
|
A | G | 1 | a0001c0003t0014g0319 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-124+7003T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078898 | ||||||
chr2:206079226
|
C | T | 1 | a0001c0011t0043g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-124+6675G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206079226 | ||||||
chr2:206079269
|
C | T | 25 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-124+6632G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206079269 | ||||||
chr2:206079305
|
T | C | 88 | a0001c0001t0003g0282a0001c0003t0002g0247a0001c0003t0002g0249others(85): Show | 88 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-124+6596A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206079305 | ||||||
chr2:206079813
|
C | T | 1 | a0001c0003t0006g0291 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-124+6088G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206079813 | ||||||
chr2:206080089
|
C | T | 1 | a0002c0002t0001g0106 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-124+5812G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080089 | ||||||
chr2:206080304
|
G | A | 25 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-124+5597C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080304 | ||||||
chr2:206080345
|
C | T | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+5556G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080345 | ||||||
chr2:206080351
|
G | C | 216 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(213): Show | 218 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.-124+5550C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080351 | ||||||
chr2:206080390
|
G | A | 1 | a0001c0001t0012g0086 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-124+5511C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080390 | ||||||
chr2:206080630
|
G | A | 89 | a0001c0001t0003g0282a0001c0001t0038g0287a0001c0003t0002g0247others(86): Show | 89 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.-124+5271C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080630 | ||||||
chr2:206080652
|
T | A | 4 | a0001c0001t0003g0074a0001c0001t0005g0232a0001c0001t0005g0233others(1): Show | 4 | HG00621.hp2 NA18947.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-124+5249A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080652 | ||||||
chr2:206080692
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-124+5209C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080692 | ||||||
chr2:206080702
|
C | T | 1 | a0001c0001t0032g0045 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-124+5199G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080702 | ||||||
chr2:206080724
|
G | A | 67 | a0001c0001t0003g0002a0001c0001t0003g0282a0001c0001t0038g0287others(64): Show | 68 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-124+5177C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080724 | ||||||
chr2:206080724
|
G | C | 1 | a0001c0001t0005g0233 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-124+5177C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080724 | ||||||
chr2:206080735
|
G | A | 1 | a0006c0014t0003g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-124+5166C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080735 | ||||||
chr2:206080858
|
G | C | 4 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212others(1): Show | 4 | HG01123.hp2 HG03710.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-124+5043C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080858 | ||||||
chr2:206080859
|
T | C | 4 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212others(1): Show | 4 | HG01123.hp2 HG03710.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-124+5042A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080859 | ||||||
chr2:206080879
|
G | A | 1 | a0001c0001t0005g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-124+5022C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080879 | ||||||
chr2:206080902
|
C | CA | 24 | a0001c0001t0005g0224a0001c0003t0002g0199a0001c0003t0002g0289others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.-124+4998dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080902 | ||||||
chr2:206080902
|
C | CAA | 19 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(16): Show | 19 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.-124+4997_-124+499 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080902 | ||||||
chr2:206080902
|
C | CAAA | 13 | a0001c0001t0002g0033a0001c0001t0005g0088a0001c0001t0005g0089others(10): Show | 13 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-124+4996_-124+499 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080902 | ||||||
chr2:206080902
|
C | CAAAA | 6 | a0001c0001t0008g0243a0001c0001t0013g0035a0001c0001t0022g0032others(3): Show | 6 | HG01109.hp2 HG02257.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+4995_-124+499 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080902 | ||||||
chr2:206080902
|
CA | C | 79 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(76): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-124+4998delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080902 | ||||||
chr2:206080928
|
G | A | 24 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(21): Show | 24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-124+4973C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080928 | ||||||
chr2:206080931
|
T | A | 2 | a0001c0001t0005g0235a0001c0001t0005g0237 | 2 | HG00558.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-124+4970A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080931 | ||||||
chr2:206081177
|
A | G | 1 | a0002c0005t0040g0326 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-124+4724T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081177 | ||||||
chr2:206081363
|
T | C | 3 | a0002c0005t0002g0327a0002c0005t0006g0328a0002c0005t0040g0326 | 3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-124+4538A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081363 | ||||||
chr2:206081528
|
G | A | 1 | a0001c0006t0001g0188 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-124+4373C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081528 | ||||||
chr2:206081612
|
G | T | 54 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(51): Show | 55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-124+4289C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081612 | ||||||
chr2:206081672
|
A | C | 12 | a0001c0004t0007g0202a0001c0004t0007g0203a0001c0004t0007g0212others(9): Show | 12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-124+4229T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081672 | ||||||
chr2:206081688
|
T | G | 6 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(3): Show | 6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+4213A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081688 | ||||||
chr2:206081756
|
C | CA | 33 | a0001c0001t0004g0001a0001c0001t0004g0012a0001c0001t0004g0014others(30): Show | 34 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-124+4144dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081756 | ||||||
chr2:206081768
|
A | AAAAG | 50 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(47): Show | 51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.-124+4129_-124+413 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081768 | ||||||
chr2:206081768
|
AAAAGAAA others(5): Show |
A | 24 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(21): Show | 24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-124+4121_-124+413 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081768 | ||||||
chr2:206081817
|
T | G | 77 | a0001c0001t0003g0282a0001c0001t0038g0287a0001c0003t0002g0247others(74): Show | 77 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.-124+4084A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081817 | ||||||
chr2:206081838
|
A | G | 1 | a0002c0002t0001g0196 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-124+4063T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081838 | ||||||
chr2:206081873
|
A | G | 2 | a0002c0002t0001g0103a0002c0002t0001g0195 | 2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-124+4028T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081873 | ||||||
chr2:206081935
|
C | T | 54 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(51): Show | 55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-124+3966G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081935 | ||||||
chr2:206081970
|
A | G | 3 | a0001c0003t0002g0257a0001c0003t0061g0256a0002c0002t0001g0194 | 3 | HG00621.hp1 NA18747.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-124+3931T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081970 | ||||||
chr2:206082107
|
G | A | 1 | a0001c0004t0037g0204 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-124+3794C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082107 | ||||||
chr2:206082247
|
G | A | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+3654C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082247 | ||||||
chr2:206082332
|
T | C | 1 | a0001c0001t0041g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-124+3569A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082332 | ||||||
chr2:206082387
|
C | T | 6 | a0001c0001t0015g0006a0001c0001t0015g0007a0001c0001t0015g0010others(3): Show | 6 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+3514G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082387 | ||||||
chr2:206082442
|
T | C | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+3459A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082442 | ||||||
chr2:206082697
|
C | A | 1 | a0001c0003t0054g0305 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-124+3204G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082697 | ||||||
chr2:206082847
|
A | G | 24 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0005g0087others(21): Show | 24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-124+3054T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082847 | ||||||
chr2:206082929
|
T | A | 1 | a0001c0004t0011g0214 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-124+2972A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082929 | ||||||
chr2:206083400
|
G | T | 88 | a0001c0001t0003g0282a0001c0001t0038g0287a0001c0003t0002g0247others(85): Show | 88 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.-124+2501C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083400 | ||||||
chr2:206083440
|
T | C | 1 | a0001c0003t0002g0316 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-124+2461A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083440 | ||||||
chr2:206083530
|
C | A | 2 | a0001c0001t0003g0043a0001c0001t0003g0044 | 2 | NA19010.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-124+2371G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083530 | ||||||
chr2:206083535
|
C | G | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+2366G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083535 | ||||||
chr2:206083627
|
A | G | 2 | a0001c0008t0019g0205a0001c0008t0019g0206 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-124+2274T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083627 | ||||||
chr2:206083682
|
C | G | 1 | a0002c0002t0001g0193 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-124+2219G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083682 | ||||||
chr2:206083824
|
A | G | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+2077T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083824 | ||||||
chr2:206083860
|
C | CA | 73 | a0001c0001t0003g0090a0001c0001t0003g0282a0001c0001t0013g0036others(70): Show | 73 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-124+2040dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083860 | ||||||
chr2:206083860
|
C | CAA | 19 | a0001c0003t0002g0293a0001c0003t0002g0294a0001c0003t0002g0297others(16): Show | 19 | HG00673.hp1 HG01175.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-124+2039_-124+204 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083860 | ||||||
chr2:206083860
|
CA | C | 55 | a0001c0001t0002g0208a0001c0001t0002g0230a0001c0001t0004g0001others(52): Show | 56 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.-124+2040delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083860 | ||||||
chr2:206084074
|
C | CT | 28 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(25): Show | 29 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-124+1826dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084074 | ||||||
chr2:206084086
|
T | G | 1 | a0001c0003t0002g0306 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-124+1815A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084086 | ||||||
chr2:206084213
|
AT | A | 27 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(24): Show | 28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+1687delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084213 | ||||||
chr2:206084215
|
T | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+1686A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084215 | ||||||
chr2:206084238
|
CAT | C | 3 | a0001c0001t0022g0032a0001c0001t0041g0213a0001c0001t0042g0031 | 3 | HG01109.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-124+1661_-124+166 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084238 | ||||||
chr2:206084240
|
T | C | 4 | a0001c0001t0002g0033a0001c0001t0013g0035a0001c0001t0013g0036others(1): Show | 4 | HG02257.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-124+1661A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | ||||||
chr2:206084240
|
T | TAC | 12 | a0001c0001t0005g0236a0001c0003t0002g0199a0001c0004t0011g0214others(9): Show | 12 | HG00140.hp2 HG00621.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-124+1659_-124+166 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | ||||||
chr2:206084240
|
T | TACAC | 9 | a0001c0004t0007g0216a0001c0004t0007g0218a0001c0004t0007g0220others(6): Show | 9 | HG00639.hp2 HG01175.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-124+1657_-124+166 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | ||||||
chr2:206084240
|
TAC | T | 38 | a0001c0001t0002g0208a0001c0001t0003g0085a0001c0001t0004g0001others(35): Show | 39 | HG00673.hp2 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-124+1659_-124+166 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | ||||||
chr2:206084240
|
TACAC | T | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-124+1657_-124+166 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | ||||||
chr2:206084240
|
TACACAC | T | 14 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-124+1655_-124+166 others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | ||||||
chr2:206084271
|
A | ACC | 7 | a0001c0003t0002g0247a0001c0003t0002g0249a0001c0003t0002g0250others(4): Show | 7 | HG03669.hp2 NA18945.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+1629_-124+163 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084271 | ||||||
chr2:206084273
|
A | ACACC | 13 | a0001c0003t0002g0308a0001c0003t0002g0310a0001c0003t0002g0314others(10): Show | 13 | HG01123.hp2 HG02486.hp2 HG03098.hp2 others(10): Show |
intron_variant | MODIFIER | c.-124+1627_-124+162 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084273 | ||||||
chr2:206084273
|
A | ACC | 55 | a0001c0001t0003g0282a0001c0001t0038g0287a0001c0003t0002g0257others(52): Show | 55 | HG00099.hp2 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-124+1626_-124+162 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084273 | ||||||
chr2:206084273
|
A | C | 10 | a0001c0003t0002g0247a0001c0003t0002g0249a0001c0003t0002g0250others(7): Show | 10 | HG01074.hp1 HG02523.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-124+1628T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084273 | ||||||
chr2:206084354
|
T | C | 1 | a0001c0003t0006g0321 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-124+1547A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084354 | ||||||
chr2:206084527
|
A | G | 76 | a0001c0001t0003g0282a0001c0001t0038g0287a0001c0003t0002g0247others(73): Show | 76 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.-124+1374T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084527 | ||||||
chr2:206084617
|
G | A | 1 | a0001c0001t0003g0090 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-124+1284C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084617 | ||||||
chr2:206084684
|
C | T | 1 | a0002c0002t0001g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-124+1217G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084684 | ||||||
chr2:206084819
|
T | C | 1 | a0001c0001t0005g0237 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-124+1082A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084819 | ||||||
chr2:206084929
|
G | A | 17 | a0001c0001t0002g0230a0001c0001t0005g0224a0001c0001t0005g0227others(14): Show | 17 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.-124+972C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084929 | ||||||
chr2:206085136
|
G | A | 7 | a0001c0001t0008g0238a0001c0001t0008g0240a0001c0001t0008g0241others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+765C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085136 | ||||||
chr2:206085163
|
G | A | 217 | a0001c0001t0002g0033a0001c0001t0002g0208a0001c0001t0002g0230others(214): Show | 219 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-124+738C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085163 | ||||||
chr2:206085308
|
T | G | 2 | a0002c0002t0010g0244a0002c0002t0046g0245 | 2 | NA18989.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-124+593A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085308 | ||||||
chr2:206085366
|
G | A | 1 | a0001c0001t0031g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+535C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085366 | ||||||
chr2:206085445
|
C | T | 8 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(5): Show | 8 | HG02135.hp2 NA18940.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.-124+456G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085445 | ||||||
chr2:206085512
|
G | C | 107 | a0001c0001t0003g0282a0001c0001t0004g0001a0001c0001t0004g0011others(104): Show | 108 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.-124+389C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085512 | ||||||
chr2:206085526
|
G | A | 3 | a0002c0005t0002g0327a0002c0005t0006g0328a0002c0005t0040g0326 | 3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-124+375C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085526 | ||||||
chr2:206085560
|
G | A | 1 | a0001c0001t0009g0329 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-124+341C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085560 | ||||||
chr2:206085594
|
C | G | 56 | a0001c0001t0003g0002a0001c0001t0003g0039a0001c0001t0003g0040others(53): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-124+307G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085594 | ||||||
chr2:206085602
|
C | T | 7 | a0001c0001t0002g0033a0001c0001t0013g0030a0001c0001t0013g0035others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+299G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085602 |