geneid | 145501 |
---|---|
ensemblid | ENSG00000100593.18 |
hgncid | 23176 |
symbol | ISM2 |
name | isthmin 2 |
refseq_nuc | NM_199296.3 |
refseq_prot | NP_954993.1 |
ensembl_nuc | ENST00000342219.9 |
ensembl_prot | ENSP00000341490.4 |
mane_status | MANE Select |
chr | chr14 |
start | 77474394 |
end | 77498816 |
strand | - |
ver | v1.2 |
region | chr14:77474394-77498816 |
region5000 | chr14:77469394-77503816 |
regionname0 | ISM2_chr14_77474394_77498816 |
regionname5000 | ISM2_chr14_77469394_77503816 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 571 | 137 | 15 | 37 | 57 | 7 | 20 | 35 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002 | 1/0 | 571 | 120 | 63 | 24 | 8 | 6 | 18 | 7 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0003 | 0/0 | 571 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0004 | 0/0 | 571 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0005 | 0/0 | 571 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0006 | 0/0 | 571 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0007 | 0/0 | 571 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0008 | 0/0 | 571 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0009 | 0/0 | 571 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0010 | 0/0 | 571 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0011 | 0/0 | 571 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0012 | 0/0 | 571 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0013 | 0/0 | 571 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
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 | 1716 | 128 | 14 | 36 | 51 | 6 | 20 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0002 | 1/0 | 1716 | 96 | 58 | 15 | 4 | 5 | 13 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0003 | 0/0 | 1716 | 14 | 1 | 6 | 3 | 1 | 3 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0004 | 0/0 | 1716 | 8 | 8 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0005 | 0/0 | 1716 | 3 | 0 | 0 | 3 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0006 | 0/0 | 1716 | 3 | 0 | 3 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0007 | 0/0 | 1716 | 3 | 2 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0008 | 0/0 | 1716 | 3 | 0 | 1 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0009 | 0/0 | 1716 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0010 | 0/0 | 1716 | 2 | 0 | 0 | 1 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0011 | 0/0 | 1716 | 2 | 0 | 0 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0012 | 0/0 | 1716 | 2 | 0 | 0 | 2 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0013 | 0/0 | 1716 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0014 | 0/0 | 1716 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0015 | 0/0 | 1716 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0016 | 0/0 | 1716 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0017 | 0/0 | 1716 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0018 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0019 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0020 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0021 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0022 | 0/0 | 1716 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
c0023 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
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 | 0/1 | 1235 | 210 | 49 | 57 | 60 | 12 | 31 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0002 | 0/0 | 1224 | 26 | 9 | 5 | 2 | 2 | 8 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0003 | 1/0 | 1225 | 20 | 18 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0004 | 0/0 | 1235 | 5 | 4 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0005 | 0/0 | 1224 | 3 | 2 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0006 | 0/0 | 1235 | 3 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0007 | 0/0 | 1235 | 2 | 0 | 0 | 2 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0008 | 0/0 | 1235 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0009 | 0/0 | 1224 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0010 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0011 | 0/0 | 1235 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0012 | 0/0 | 1235 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0013 | 0/0 | 1235 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0014 | 0/0 | 1235 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0015 | 0/0 | 1235 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0016 | 0/0 | 1235 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
t0017 | 0/0 | 1235 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
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 | 3 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
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 | 1716 | 128 | 14 | 36 | 51 | 6 | 20 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0005 | 0/0 | 1716 | 3 | 0 | 0 | 3 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0009 | 0/0 | 1716 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0010 | 0/0 | 1716 | 2 | 0 | 0 | 1 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0012 | 0/0 | 1716 | 2 | 0 | 0 | 2 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0002 | 1/0 | 1716 | 96 | 58 | 15 | 4 | 5 | 13 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0003 | 0/0 | 1716 | 14 | 1 | 6 | 3 | 1 | 3 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0007 | 0/0 | 1716 | 3 | 2 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0008 | 0/0 | 1716 | 3 | 0 | 1 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0015 | 0/0 | 1716 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0021 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0023 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0003c0004 | 0/0 | 1716 | 8 | 8 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0004c0006 | 0/0 | 1716 | 3 | 0 | 3 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0005c0014 | 0/0 | 1716 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0006c0013 | 0/0 | 1716 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0007c0011 | 0/0 | 1716 | 2 | 0 | 0 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0008c0016 | 0/0 | 1716 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0009c0019 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0010c0022 | 0/0 | 1716 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0011c0020 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0012c0018 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0013c0017 | 0/0 | 1716 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2950 | 120 | 11 | 35 | 48 | 6 | 19 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0001t0002 | 0/0 | 2939 | 2 | 0 | 0 | 1 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0001t0004 | 0/0 | 2950 | 3 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0001t0013 | 0/0 | 2950 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0001t0016 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0001t0017 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0005t0001 | 0/0 | 2950 | 3 | 0 | 0 | 3 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0009t0004 | 0/0 | 2950 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0010t0001 | 0/0 | 2950 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0010t0007 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0001c0012t0001 | 0/0 | 2950 | 2 | 0 | 0 | 2 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0002t0001 | 0/0 | 2950 | 44 | 24 | 9 | 3 | 3 | 5 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0002t0002 | 0/0 | 2939 | 23 | 8 | 5 | 1 | 2 | 7 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0002t0003 | 1/0 | 2940 | 19 | 18 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0002t0005 | 0/0 | 2939 | 3 | 2 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0002t0006 | 0/0 | 2950 | 3 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0002t0008 | 0/0 | 2950 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0002t0009 | 0/0 | 2939 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0002t0011 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0003t0001 | 0/0 | 2950 | 13 | 1 | 6 | 2 | 1 | 3 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0003t0007 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0007t0001 | 0/0 | 2950 | 2 | 1 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0007t0015 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0008t0001 | 0/0 | 2950 | 3 | 0 | 1 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0015t0001 | 0/0 | 2950 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0021t0002 | 0/0 | 2939 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0002c0023t0012 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0003c0004t0001 | 0/0 | 2950 | 8 | 8 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0004c0006t0001 | 0/0 | 2950 | 3 | 0 | 3 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0005c0014t0001 | 0/0 | 2950 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0006c0013t0001 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0006c0013t0014 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0007c0011t0001 | 0/0 | 2950 | 2 | 0 | 0 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0008c0016t0003 | 0/0 | 2940 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0009c0019t0010 | 0/0 | 2939 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0010c0022t0001 | 0/0 | 2950 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0011c0020t0001 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0012c0018t0001 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
a0013c0017t0001 | 0/0 | 2950 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | copy fasta | chr14 | 77469394 | 77503816 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0013g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0016g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0001t0017g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0005t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0009t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0009t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0010t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0010t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0012t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0001c0012t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0005g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0009g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0002t0011g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0003t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0007t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0007t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0007t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0008t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0008t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0008t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0015t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0021t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0002c0023t0012g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0003c0004t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0003c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0003c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0003c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0003c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0003c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0003c0004t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0004c0006t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0004c0006t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0004c0006t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0005c0014t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0005c0014t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0006c0013t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0006c0013t0014g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0007c0011t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0007c0011t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0008c0016t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0009c0019t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0010c0022t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0011c0020t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0012c0018t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
a0013c0017t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0010 | t0001 | g0143 | EUR | GBR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0067 | EUR | GBR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00140 | hp2 | a0013 | c0017 | t0001 | g0029 | EUR | GBR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0109 | EUR | FIN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00642 | hp1 | a0002 | c0015 | t0001 | g0015 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00735 | hp1 | a0002 | c0015 | t0001 | g0015 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00741 | hp1 | a0002 | c0003 | t0001 | g0256 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01069 | hp2 | a0001 | c0001 | t0013 | g0050 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01070 | hp1 | a0002 | c0008 | t0001 | g0190 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01070 | hp2 | a0004 | c0006 | t0001 | g0229 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01071 | hp2 | a0004 | c0006 | t0001 | g0232 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01109 | hp1 | a0001 | c0009 | t0004 | g0088 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0168 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01192 | hp1 | a0004 | c0006 | t0001 | g0235 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01243 | hp1 | a0002 | c0002 | t0005 | g0009 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01255 | hp1 | a0002 | c0003 | t0001 | g0249 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01257 | hp1 | a0002 | c0003 | t0001 | g0016 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0211 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0171 | EUR | IBS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0162 | EUR | IBS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0238 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01891 | hp1 | a0002 | c0002 | t0008 | g0076 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01891 | hp2 | a0002 | c0002 | t0003 | g0117 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0206 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01981 | hp1 | a0010 | c0022 | t0001 | g0248 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01993 | hp1 | a0002 | c0003 | t0001 | g0257 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02074 | hp1 | a0012 | c0018 | t0001 | g0155 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0210 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02148 | hp2 | a0002 | c0003 | t0001 | g0259 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CDX | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02165 | hp2 | a0001 | c0001 | t0017 | g0114 | EAS | CDX | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02257 | hp2 | a0002 | c0002 | t0003 | g0122 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02280 | hp1 | a0003 | c0004 | t0001 | g0028 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0202 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0080 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02630 | hp2 | a0002 | c0002 | t0003 | g0019 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02647 | hp1 | a0002 | c0002 | t0003 | g0057 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0165 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02698 | hp1 | a0002 | c0003 | t0001 | g0251 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0116 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02717 | hp1 | a0005 | c0014 | t0001 | g0027 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02723 | hp1 | a0002 | c0002 | t0003 | g0118 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0198 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0068 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02735 | hp2 | a0002 | c0003 | t0001 | g0252 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0071 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0108 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02818 | hp1 | a0002 | c0002 | t0008 | g0075 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02818 | hp2 | a0002 | c0002 | t0005 | g0009 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02886 | hp2 | a0002 | c0007 | t0015 | g0059 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02895 | hp2 | a0003 | c0004 | t0001 | g0004 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0245 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02922 | hp1 | a0002 | c0002 | t0005 | g0119 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02922 | hp2 | a0002 | c0002 | t0006 | g0079 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02965 | hp1 | a0002 | c0002 | t0006 | g0065 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02965 | hp2 | a0002 | c0023 | t0012 | g0261 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02970 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02970 | hp2 | a0003 | c0004 | t0001 | g0023 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0107 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0163 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0087 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0160 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03098 | hp1 | a0002 | c0002 | t0003 | g0201 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0247 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03130 | hp1 | a0003 | c0004 | t0001 | g0024 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03130 | hp2 | a0002 | c0002 | t0003 | g0086 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03139 | hp1 | a0002 | c0002 | t0003 | g0204 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03139 | hp2 | a0002 | c0007 | t0001 | g0020 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0152 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03195 | hp2 | a0005 | c0014 | t0001 | g0026 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03209 | hp1 | a0002 | c0002 | t0003 | g0158 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03225 | hp1 | a0003 | c0004 | t0001 | g0022 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03225 | hp2 | a0003 | c0004 | t0001 | g0197 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03239 | hp2 | a0007 | c0011 | t0001 | g0156 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03486 | hp1 | a0006 | c0013 | t0014 | g0111 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0121 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0188 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0125 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03540 | hp1 | a0002 | c0002 | t0011 | g0244 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03540 | hp2 | a0002 | c0002 | t0003 | g0157 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03579 | hp1 | a0003 | c0004 | t0001 | g0025 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0167 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03704 | hp1 | a0002 | c0008 | t0001 | g0030 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0227 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0013 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0070 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0164 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG04199 | hp2 | a0002 | c0002 | t0009 | g0208 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG04204 | hp1 | a0002 | c0003 | t0001 | g0253 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG04228 | hp2 | a0002 | c0008 | t0001 | g0192 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18522 | hp1 | a0002 | c0002 | t0003 | g0018 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18946 | hp2 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18967 | hp1 | a0002 | c0003 | t0007 | g0260 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18969 | hp2 | a0002 | c0007 | t0001 | g0055 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18990 | hp1 | a0001 | c0010 | t0007 | g0239 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19000 | hp1 | a0001 | c0012 | t0001 | g0149 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19011 | hp2 | a0001 | c0005 | t0001 | g0141 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0243 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19043 | hp1 | a0002 | c0002 | t0006 | g0195 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0120 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19063 | hp2 | a0001 | c0005 | t0001 | g0135 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19066 | hp2 | a0001 | c0012 | t0001 | g0140 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19074 | hp2 | a0001 | c0001 | t0016 | g0128 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19081 | hp2 | a0002 | c0003 | t0001 | g0254 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19083 | hp2 | a0001 | c0005 | t0001 | g0134 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0081 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA20129 | hp1 | a0002 | c0002 | t0003 | g0085 | AFR | ASW | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ASW | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA20752 | hp2 | a0002 | c0003 | t0001 | g0258 | EUR | TSI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0110 | EUR | TSI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA20905 | hp1 | a0007 | c0011 | t0001 | g0133 | SAS | GIH | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | GIH | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01123 | hp1 | a0002 | c0003 | t0001 | g0250 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG01123 | hp2 | a0008 | c0016 | t0003 | g0205 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02109 | hp1 | a0003 | c0004 | t0001 | g0004 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02109 | hp2 | a0002 | c0002 | t0003 | g0010 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02486 | hp1 | a0009 | c0019 | t0010 | g0207 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0151 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0159 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG06807 | hp1 | a0011 | c0020 | t0001 | g0196 | AFR | USA | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
HG06807 | hp2 | a0001 | c0009 | t0004 | g0072 | AFR | USA | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA20300 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | USA | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA20300 | hp2 | a0002 | c0002 | t0003 | g0010 | AFR | USA | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA21309 | hp1 | a0002 | c0021 | t0002 | g0017 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
NA21309 | hp2 | a0006 | c0013 | t0001 | g0112 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0073 | REF | REF | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0003 | g0203 | REF | REF | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77475696
|
G | A | 1 | a0011 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1615C>T | p.Arg539Cys | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1638/2940 | 1615/1716 | 539/571 | chr14 | 77475696 | ||
chr14:77475882
|
G | A | 1 | a0006 | 2 | HG03486.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1429C>T | p.Arg477Cys | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1452/2940 | 1429/1716 | 477/571 | chr14 | 77475882 | ||
chr14:77475929
|
G | A | 1 | a0010 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.1382C>T | p.Pro461Leu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1405/2940 | 1382/1716 | 461/571 | chr14 | 77475929 | ||
chr14:77478253
|
A | G | 1 | a0012 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.1187T>C | p.Met396Thr | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/7 | 1210/2940 | 1187/1716 | 396/571 | chr14 | 77478253 | ||
chr14:77478281
|
T | C | 1 | a0007 | 2 | HG03239.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.1159A>G | p.Lys387Glu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/7 | 1182/2940 | 1159/1716 | 387/571 | chr14 | 77478281 | ||
chr14:77482494
|
C | G | 1 | a0009 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.801G>C | p.Glu267Asp | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/7 | 824/2940 | 801/1716 | 267/571 | chr14 | 77482494 | ||
chr14:77482498
|
C | T | 1 | a0005 | 2 | HG02717.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.797G>A | p.Gly266Glu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/7 | 820/2940 | 797/1716 | 266/571 | chr14 | 77482498 | ||
chr14:77482594
|
G | A | 1 | a0004 | 3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
missense_variant | MODERATE | c.701C>T | p.Pro234Leu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/7 | 724/2940 | 701/1716 | 234/571 | chr14 | 77482594 | ||
chr14:77484513
|
A | T | 1 | a0013 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.437T>A | p.Leu146Gln | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/7 | 460/2940 | 437/1716 | 146/571 | chr14 | 77484513 | ||
chr14:77484553
|
G | C | 2 | a0003a0005 | 10 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(7): Show |
missense_variant | MODERATE | c.397C>G | p.Pro133Ala | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/7 | 420/2940 | 397/1716 | 133/571 | chr14 | 77484553 | ||
chr14:77484781
|
C | T | 5 | a0001a0004a0007others(2): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
missense_variant | MODERATE | c.280G>A | p.Ala94Thr | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 2/7 | 303/2940 | 280/1716 | 94/571 | chr14 | 77484781 | ||
chr14:77484865
|
G | T | 1 | a0008 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.196C>A | p.Leu66Ile | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 2/7 | 219/2940 | 196/1716 | 66/571 | chr14 | 77484865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77475736
|
G | A | 1 | a0001c0005 | 3 | NA19011.hp2 NA19063.hp2 NA19083.hp2 |
synonymous_variant | LOW | c.1575C>T | p.Phe525Phe | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1598/2940 | 1575/1716 | 525/571 | chr14 | 77475736 | ||
chr14:77475766
|
G | A | 1 | a0001c0009 | 2 | HG01109.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.1545C>T | p.Thr515Thr | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1568/2940 | 1545/1716 | 515/571 | chr14 | 77475766 | ||
chr14:77475973
|
G | A | 4 | a0001c0010a0002c0003a0002c0007others(1): Show | 20 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(17): Show |
synonymous_variant | LOW | c.1338C>T | p.Asp446Asp | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1361/2940 | 1338/1716 | 446/571 | chr14 | 77475973 | ||
chr14:77478609
|
G | A | 1 | a0001c0012 | 2 | NA19000.hp1 NA19066.hp2 |
synonymous_variant | LOW | c.1080C>T | p.Thr360Thr | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 5/7 | 1103/2940 | 1080/1716 | 360/571 | chr14 | 77478609 | ||
chr14:77482323
|
G | A | 1 | a0002c0021 | 1 | NA21309.hp1 | splice_region_variant&synonymous_variant | LOW | c.972C>T | p.Tyr324Tyr | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/7 | 995/2940 | 972/1716 | 324/571 | chr14 | 77482323 | ||
chr14:77484800
|
T | C | 1 | a0002c0008 | 3 | HG01070.hp1 HG03704.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.261A>G | p.Ala87Ala | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 2/7 | 284/2940 | 261/1716 | 87/571 | chr14 | 77484800 | ||
chr14:77498751
|
G | A | 3 | a0002c0003a0002c0015a0010c0022 | 17 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
synonymous_variant | LOW | c.43C>T | p.Leu15Leu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/7 | 66/2940 | 43/1716 | 15/571 | chr14 | 77498751 | ||
chr14:77498758
|
G | A | 1 | a0002c0023 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.36C>T | p.Leu12Leu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/7 | 59/2940 | 36/1716 | 12/571 | chr14 | 77498758 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77474403
|
A | T | 1 | a0009c0019t0010 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1192T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1192 | chr14 | 77474403 | |||||
chr14:77474484
|
G | A | 2 | a0001c0001t0004a0001c0009t0004 | 5 | HG01109.hp1 HG02145.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1111C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1111 | chr14 | 77474484 | |||||
chr14:77474517
|
T | C | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(34): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*1078A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1078 | chr14 | 77474517 | |||||
chr14:77474526
|
C | A | 1 | a0002c0007t0015 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1069G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1069 | chr14 | 77474526 | |||||
chr14:77474590
|
C | T | 1 | a0002c0002t0009 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1005 | chr14 | 77474590 | |||||
chr14:77474623
|
C | G | 1 | a0006c0013t0014 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 972 | chr14 | 77474623 | |||||
chr14:77474831
|
C | T | 1 | a0001c0001t0013 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*764G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 764 | chr14 | 77474831 | |||||
chr14:77474947
|
G | A | 2 | a0001c0010t0007a0002c0003t0007 | 2 | NA18967.hp1 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*648C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 648 | chr14 | 77474947 | |||||
chr14:77475099
|
A | T | 1 | a0002c0002t0011 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*496T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 496 | chr14 | 77475099 | |||||
chr14:77475102
|
C | T | 2 | a0002c0002t0011a0002c0023t0012 | 2 | HG02965.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*493G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 493 | chr14 | 77475102 | |||||
chr14:77475103
|
A | G | 32 | a0001c0001t0001a0001c0001t0004a0001c0001t0013others(29): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*492T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 492 | chr14 | 77475103 | |||||
chr14:77475111
|
T | C | 1 | a0001c0001t0016 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 484 | chr14 | 77475111 | |||||
chr14:77475112
|
GC | G | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(34): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*482delG | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 482 | chr14 | 77475112 | |||||
chr14:77475120
|
C | A | 1 | a0002c0002t0008 | 2 | HG01891.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*475G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 475 | chr14 | 77475120 | |||||
chr14:77475445
|
G | A | 1 | a0009c0019t0010 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*150C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 150 | chr14 | 77475445 | |||||
chr14:77475480
|
C | T | 2 | a0002c0002t0011a0002c0023t0012 | 2 | HG02965.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 115 | chr14 | 77475480 | |||||
chr14:77475522
|
G | GAGGGCCC others(4): Show |
31 | a0001c0001t0001a0001c0001t0004a0001c0001t0013others(28): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*72_*73insGGTAGGGC others(3): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 72 | chr14 | 77475522 | |||||
chr14:77475537
|
G | A | 1 | a0001c0001t0017 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*58C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 58 | chr14 | 77475537 | |||||
chr14:77475551
|
G | A | 1 | a0002c0002t0006 | 3 | HG02922.hp2 HG02965.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*44C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 44 | chr14 | 77475551 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77476163
|
C | T | 17 | a0001c0010t0001g0143a0001c0010t0007g0239a0002c0003t0001g0016others(14): Show | 18 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1199-51G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476163 | ||||||
chr14:77476164
|
G | A | 2 | a0002c0007t0001g0020a0002c0007t0015g0059 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1199-52C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476164 | ||||||
chr14:77476172
|
C | T | 6 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(3): Show | 7 | HG02109.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1199-60G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476172 | ||||||
chr14:77476199
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1199-87C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476199 | ||||||
chr14:77476235
|
G | A | 25 | a0001c0010t0001g0143a0001c0010t0007g0239a0002c0003t0001g0016others(22): Show | 27 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1199-123C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476235 | ||||||
chr14:77476267
|
G | C | 1 | a0002c0002t0001g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1199-155C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476267 | ||||||
chr14:77476269
|
T | C | 1 | a0008c0016t0003g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1199-157A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476269 | ||||||
chr14:77476650
|
C | T | 4 | a0002c0002t0003g0085a0002c0002t0003g0117a0002c0002t0003g0120others(1): Show | 4 | HG01891.hp2 HG03486.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199-538G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476650 | ||||||
chr14:77476664
|
A | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1199-552T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476664 | ||||||
chr14:77476727
|
A | G | 1 | a0002c0002t0003g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1199-615T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476727 | ||||||
chr14:77476776
|
G | A | 2 | a0002c0002t0011g0244a0002c0023t0012g0261 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1199-664C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476776 | ||||||
chr14:77476779
|
A | G | 2 | a0002c0002t0011g0244a0002c0023t0012g0261 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1199-667T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476779 | ||||||
chr14:77477089
|
A | G | 6 | a0001c0001t0001g0069a0002c0002t0001g0067a0002c0002t0001g0070others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1199-977T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477089 | ||||||
chr14:77477132
|
A | G | 6 | a0002c0002t0001g0058a0002c0002t0001g0153a0002c0002t0001g0154others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1199-1020T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477132 | ||||||
chr14:77477135
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1199-1023C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477135 | ||||||
chr14:77477230
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1198+1012A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477230 | ||||||
chr14:77477273
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1198+969G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477273 | ||||||
chr14:77477305
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1198+937G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477305 | ||||||
chr14:77477326
|
G | A | 6 | a0001c0001t0004g0226a0001c0001t0004g0241a0001c0001t0004g0243others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1198+916C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477326 | ||||||
chr14:77477370
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1198+872A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477370 | ||||||
chr14:77477499
|
G | A | 17 | a0001c0010t0001g0143a0001c0010t0007g0239a0002c0003t0001g0016others(14): Show | 18 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1198+743C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477499 | ||||||
chr14:77477726
|
C | A | 1 | a0002c0002t0001g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1198+516G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477726 | ||||||
chr14:77477815
|
G | A | 2 | a0002c0002t0011g0244a0002c0023t0012g0261 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1198+427C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477815 | ||||||
chr14:77477904
|
G | T | 2 | a0002c0002t0011g0244a0002c0023t0012g0261 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1198+338C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477904 | ||||||
chr14:77477918
|
C | T | 2 | a0005c0014t0001g0026a0005c0014t0001g0027 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1198+324G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477918 | ||||||
chr14:77477951
|
C | T | 1 | a0002c0002t0001g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1198+291G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477951 | ||||||
chr14:77478360
|
G | C | 1 | a0003c0004t0001g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1115-35C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 5/6 | chr14 | 77478360 | ||||||
chr14:77478382
|
A | G | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0173others(1): Show | 4 | HG02015.hp2 HG02523.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-57T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 5/6 | chr14 | 77478382 | ||||||
chr14:77478395
|
C | T | 1 | a0002c0007t0015g0059 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1115-70G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 5/6 | chr14 | 77478395 | ||||||
chr14:77478428
|
C | T | 6 | a0001c0001t0001g0178a0001c0001t0001g0215a0001c0001t0001g0231others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-103G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 5/6 | chr14 | 77478428 | ||||||
chr14:77478728
|
A | G | 2 | a0002c0002t0011g0244a0002c0023t0012g0261 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.974-13T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478728 | ||||||
chr14:77478744
|
G | C | 1 | a0002c0003t0001g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.974-29C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478744 | ||||||
chr14:77478803
|
T | A | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.974-88A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478803 | ||||||
chr14:77478848
|
G | A | 2 | a0002c0002t0011g0244a0002c0023t0012g0261 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.974-133C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478848 | ||||||
chr14:77478946
|
C | T | 2 | a0002c0002t0011g0244a0002c0023t0012g0261 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.974-231G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478946 | ||||||
chr14:77478976
|
T | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.974-261A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478976 | ||||||
chr14:77479157
|
C | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0234 | 3 | HG02071.hp1 NA18612.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.974-442G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479157 | ||||||
chr14:77479157
|
C | T | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.974-442G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479157 | ||||||
chr14:77479347
|
C | T | 210 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.974-632G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479347 | ||||||
chr14:77479385
|
A | AT | 25 | a0001c0010t0001g0143a0001c0010t0007g0239a0002c0002t0003g0201others(22): Show | 27 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.974-671dupA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479385 | ||||||
chr14:77479426
|
C | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.974-711G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479426 | ||||||
chr14:77479550
|
A | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.974-835T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479550 | ||||||
chr14:77479596
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.974-881G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479596 | ||||||
chr14:77479706
|
C | T | 1 | a0001c0001t0004g0241 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.974-991G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479706 | ||||||
chr14:77480295
|
A | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.974-1580T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480295 | ||||||
chr14:77480302
|
CAA | C | 70 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.974-1589_974-1588d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480302 | ||||||
chr14:77480402
|
G | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.974-1687C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480402 | ||||||
chr14:77480441
|
C | T | 2 | a0002c0002t0006g0065a0002c0002t0006g0079 | 2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.974-1726G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480441 | ||||||
chr14:77480444
|
A | G | 1 | a0002c0002t0003g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.974-1729T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480444 | ||||||
chr14:77480491
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.974-1776C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480491 | ||||||
chr14:77480547
|
CCT | C | 5 | a0001c0001t0004g0226a0001c0001t0004g0243a0001c0009t0004g0072others(2): Show | 5 | HG01109.hp1 HG02809.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.973+1773_973+1774d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480547 | ||||||
chr14:77480548
|
CT | C | 22 | a0002c0002t0001g0070a0002c0002t0001g0077a0002c0002t0001g0189others(19): Show | 24 | HG01070.hp1 HG01243.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.973+1773delA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480548 | ||||||
chr14:77480548
|
CTT | C | 41 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0001t0001g0063others(38): Show | 46 | HG00099.hp2 HG00323.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.973+1772_973+1773d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480548 | ||||||
chr14:77480548
|
CTTT | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.973+1771_973+1773d others(5): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480548 | ||||||
chr14:77480548
|
CTTTT | C | 32 | a0001c0005t0001g0135a0001c0010t0001g0143a0001c0010t0007g0239others(29): Show | 34 | HG00099.hp1 HG00741.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.973+1770_973+1773d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480548 | ||||||
chr14:77480595
|
T | TCACC | 26 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0003others(23): Show | 30 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.973+1723_973+1726d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480595 | ||||||
chr14:77480633
|
C | G | 1 | a0002c0002t0001g0109 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.973+1689G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480633 | ||||||
chr14:77480695
|
C | CTACA | 63 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(60): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.973+1623_973+1626d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480695 | ||||||
chr14:77480713
|
G | A | 181 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.973+1609C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480713 | ||||||
chr14:77480734
|
T | G | 25 | a0001c0010t0001g0143a0001c0010t0007g0239a0002c0003t0001g0016others(22): Show | 27 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.973+1588A>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480734 | ||||||
chr14:77480769
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.973+1553T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480769 | ||||||
chr14:77480834
|
A | C | 1 | a0002c0002t0011g0244 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.973+1488T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480834 | ||||||
chr14:77480855
|
G | A | 3 | a0002c0002t0001g0014a0002c0002t0001g0246a0002c0002t0001g0247 | 4 | HG02451.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.973+1467C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480855 | ||||||
chr14:77480901
|
G | A | 1 | a0002c0002t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.973+1421C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480901 | ||||||
chr14:77480955
|
A | G | 30 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0003others(27): Show | 34 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.973+1367T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480955 | ||||||
chr14:77481005
|
T | A | 1 | a0002c0002t0011g0244 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.973+1317A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481005 | ||||||
chr14:77481156
|
C | T | 52 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(49): Show | 54 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.973+1166G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481156 | ||||||
chr14:77481189
|
A | C | 1 | a0002c0002t0006g0195 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.973+1133T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481189 | ||||||
chr14:77481266
|
G | A | 1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.973+1056C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481266 | ||||||
chr14:77481339
|
C | CA | 39 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(36): Show | 40 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.973+982dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481339 | ||||||
chr14:77481342
|
A | C | 1 | a0001c0001t0001g0061 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.973+980T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481342 | ||||||
chr14:77481348
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.973+974A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481348 | ||||||
chr14:77481363
|
T | C | 6 | a0001c0001t0004g0226a0001c0001t0004g0241a0001c0001t0004g0243others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+959A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481363 | ||||||
chr14:77481488
|
A | G | 6 | a0001c0001t0004g0226a0001c0001t0004g0241a0001c0001t0004g0243others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+834T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481488 | ||||||
chr14:77481509
|
ACT | A | 6 | a0001c0001t0004g0226a0001c0001t0004g0241a0001c0001t0004g0243others(3): Show | 6 | HG01109.hp1 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+811_973+812del others(2): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481509 | ||||||
chr14:77481582
|
G | A | 13 | a0001c0001t0001g0045a0001c0001t0001g0177a0002c0002t0001g0066others(10): Show | 14 | HG00642.hp1 HG00735.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.973+740C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481582 | ||||||
chr14:77481807
|
G | GAA | 102 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 110 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.973+513_973+514dup others(2): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481807 | ||||||
chr14:77481943
|
T | TA | 6 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0092others(3): Show | 6 | HG00544.hp1 HG00544.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+378dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481943 | ||||||
chr14:77481987
|
C | G | 15 | a0001c0010t0001g0143a0002c0003t0001g0016a0002c0003t0001g0249others(12): Show | 16 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.973+335G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481987 | ||||||
chr14:77482008
|
A | T | 1 | a0003c0004t0001g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.973+314T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482008 | ||||||
chr14:77482071
|
C | G | 66 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(63): Show | 71 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.973+251G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482071 | ||||||
chr14:77482125
|
T | TA | 20 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0003others(17): Show | 24 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.973+196dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482125 | ||||||
chr14:77482125
|
TA | T | 12 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0103others(9): Show | 12 | HG01256.hp2 HG01515.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.973+196delT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482125 | ||||||
chr14:77482223
|
A | G | 22 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0003others(19): Show | 26 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.973+99T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482223 | ||||||
chr14:77482284
|
G | A | 1 | a0002c0002t0001g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.973+38C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482284 | ||||||
chr14:77482682
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628-15G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77482682 | ||||||
chr14:77482894
|
C | T | 6 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(3): Show | 7 | HG02109.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-227G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77482894 | ||||||
chr14:77482924
|
TG | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.628-258delC | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77482924 | ||||||
chr14:77483470
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.628-803G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483470 | ||||||
chr14:77483544
|
T | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.627+779A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483544 | ||||||
chr14:77483547
|
C | CA | 51 | a0001c0001t0001g0069a0002c0002t0001g0066a0002c0002t0001g0067others(48): Show | 52 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.627+775dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483547 | ||||||
chr14:77483547
|
CA | C | 12 | a0001c0001t0001g0040a0001c0001t0001g0098a0002c0003t0001g0257others(9): Show | 13 | HG01515.hp2 HG01993.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.627+775delT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483547 | ||||||
chr14:77483643
|
C | CGT | 8 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(5): Show | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.627+678_627+679dup others(2): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483643 | ||||||
chr14:77483652
|
G | C | 1 | a0002c0002t0001g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.627+671C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483652 | ||||||
chr14:77483780
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.627+543T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483780 | ||||||
chr14:77483862
|
C | T | 16 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(13): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.627+461G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483862 | ||||||
chr14:77483965
|
C | A | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.627+358G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483965 | ||||||
chr14:77484073
|
C | T | 2 | a0005c0014t0001g0026a0005c0014t0001g0027 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.627+250G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77484073 | ||||||
chr14:77484127
|
G | A | 1 | a0002c0003t0001g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.627+196C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77484127 | ||||||
chr14:77484242
|
A | G | 45 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0058others(42): Show | 52 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.627+81T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77484242 | ||||||
chr14:77484273
|
C | T | 2 | a0001c0001t0001g0225a0002c0002t0001g0094 | 2 | NA18612.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.627+50G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77484273 | ||||||
chr14:77484297
|
G | A | 9 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(6): Show | 10 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.627+26C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77484297 | ||||||
chr14:77485021
|
G | A | 52 | a0002c0002t0001g0066a0002c0002t0001g0067a0002c0002t0001g0068others(49): Show | 53 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.142-102C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485021 | ||||||
chr14:77485022
|
G | A | 2 | a0002c0002t0001g0109a0002c0002t0001g0191 | 2 | HG00323.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.142-103C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485022 | ||||||
chr14:77485088
|
C | G | 29 | a0002c0002t0001g0094a0002c0002t0001g0099a0002c0002t0001g0100others(26): Show | 30 | HG01099.hp1 HG01175.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.142-169G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485088 | ||||||
chr14:77485110
|
C | T | 8 | a0002c0002t0001g0003a0002c0002t0001g0109a0002c0002t0001g0188others(5): Show | 10 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-191G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485110 | ||||||
chr14:77485111
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.142-192C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485111 | ||||||
chr14:77485149
|
A | G | 3 | a0003c0004t0001g0197a0005c0014t0001g0026a0005c0014t0001g0027 | 3 | HG02717.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.142-230T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485149 | ||||||
chr14:77485159
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.142-240A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485159 | ||||||
chr14:77485225
|
A | G | 3 | a0003c0004t0001g0197a0005c0014t0001g0026a0005c0014t0001g0027 | 3 | HG02717.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.142-306T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485225 | ||||||
chr14:77485253
|
G | T | 36 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0058others(33): Show | 42 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.142-334C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485253 | ||||||
chr14:77485254
|
A | G | 36 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0058others(33): Show | 42 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.142-335T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485254 | ||||||
chr14:77485322
|
C | T | 2 | a0002c0007t0001g0020a0002c0007t0015g0059 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.142-403G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485322 | ||||||
chr14:77485570
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | NA19065.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.142-651T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485570 | ||||||
chr14:77485786
|
C | T | 3 | a0002c0002t0003g0018a0002c0002t0003g0019a0002c0002t0011g0244 | 3 | HG02630.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142-867G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485786 | ||||||
chr14:77486080
|
A | G | 20 | a0002c0002t0001g0066a0002c0002t0001g0067a0002c0002t0001g0068others(17): Show | 20 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-1161T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486080 | ||||||
chr14:77486267
|
T | TACTG | 185 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.142-1349_142-1348i others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486267 | ||||||
chr14:77486271
|
T | C | 2 | a0005c0014t0001g0026a0005c0014t0001g0027 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142-1352A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486271 | ||||||
chr14:77486373
|
C | A | 1 | a0003c0004t0001g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-1454G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486373 | ||||||
chr14:77486378
|
C | T | 1 | a0002c0002t0002g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-1459G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486378 | ||||||
chr14:77486389
|
A | G | 3 | a0002c0002t0003g0085a0002c0002t0003g0117a0002c0002t0003g0120 | 3 | HG01891.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.142-1470T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486389 | ||||||
chr14:77486412
|
G | A | 1 | a0008c0016t0003g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-1493C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486412 | ||||||
chr14:77486619
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-1700C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486619 | ||||||
chr14:77486685
|
G | T | 3 | a0002c0002t0006g0065a0002c0002t0006g0079a0002c0002t0006g0195 | 3 | HG02922.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.142-1766C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486685 | ||||||
chr14:77486847
|
C | G | 2 | a0001c0001t0001g0035a0002c0008t0001g0030 | 2 | HG02055.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.142-1928G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486847 | ||||||
chr14:77486864
|
G | C | 1 | a0008c0016t0003g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-1945C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486864 | ||||||
chr14:77486969
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.142-2050G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486969 | ||||||
chr14:77486979
|
C | T | 1 | a0008c0016t0003g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-2060G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486979 | ||||||
chr14:77487032
|
G | A | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142-2113C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487032 | ||||||
chr14:77487061
|
G | A | 1 | a0003c0004t0001g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-2142C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487061 | ||||||
chr14:77487103
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.142-2184C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487103 | ||||||
chr14:77487140
|
G | T | 1 | a0003c0004t0001g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-2221C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487140 | ||||||
chr14:77487159
|
C | T | 61 | a0001c0001t0001g0069a0002c0002t0001g0066a0002c0002t0001g0067others(58): Show | 63 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.142-2240G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487159 | ||||||
chr14:77487206
|
T | C | 1 | a0002c0002t0001g0110 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.142-2287A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487206 | ||||||
chr14:77487243
|
T | TTAAA | 21 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0042others(18): Show | 22 | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.142-2328_142-2325d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | ||||||
chr14:77487243
|
T | TTAAATAA others(1): Show |
13 | a0001c0001t0001g0031a0001c0001t0001g0033a0002c0002t0001g0058others(10): Show | 13 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-2332_142-2325d others(10): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | ||||||
chr14:77487243
|
T | TTAAATAA others(5): Show |
12 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0109others(9): Show | 15 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-2336_142-2325d others(14): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | ||||||
chr14:77487243
|
T | TTAAATAA others(9): Show |
7 | a0002c0002t0001g0001a0002c0002t0001g0077a0002c0002t0001g0191others(4): Show | 9 | HG01358.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-2340_142-2325d others(18): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | ||||||
chr14:77487243
|
TTAAA | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(103): Show | 114 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.142-2328_142-2325d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | ||||||
chr14:77487243
|
TTAAATAA others(1): Show |
T | 9 | a0001c0001t0001g0129a0001c0010t0007g0239a0002c0002t0003g0159others(6): Show | 10 | HG02109.hp1 HG02280.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-2332_142-2325d others(10): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | ||||||
chr14:77487243
|
TTAAATAA others(5): Show |
T | 1 | a0002c0002t0002g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142-2336_142-2325d others(14): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | ||||||
chr14:77487255
|
A | G | 16 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(13): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-2336T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487255 | ||||||
chr14:77487260
|
TA | T | 6 | a0001c0001t0001g0178a0001c0001t0001g0215a0001c0001t0001g0231others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-2342delT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487260 | ||||||
chr14:77487440
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(133): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.142-2521G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487440 | ||||||
chr14:77487466
|
A | C | 13 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0077others(10): Show | 17 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.142-2547T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487466 | ||||||
chr14:77487496
|
C | A | 2 | a0002c0002t0003g0018a0002c0002t0003g0019 | 2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.142-2577G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487496 | ||||||
chr14:77487498
|
C | A | 1 | a0002c0002t0003g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.142-2579G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487498 | ||||||
chr14:77487524
|
T | C | 2 | a0002c0002t0001g0058a0002c0002t0003g0201 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142-2605A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487524 | ||||||
chr14:77487532
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.142-2613C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487532 | ||||||
chr14:77487549
|
T | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.142-2630A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487549 | ||||||
chr14:77487663
|
G | T | 2 | a0005c0014t0001g0026a0005c0014t0001g0027 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142-2744C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487663 | ||||||
chr14:77487676
|
C | T | 4 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0002g0163others(1): Show | 4 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-2757G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487676 | ||||||
chr14:77487778
|
C | A | 7 | a0002c0002t0001g0003a0002c0002t0001g0109a0002c0002t0001g0188others(4): Show | 9 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-2859G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487778 | ||||||
chr14:77487793
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.142-2874C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487793 | ||||||
chr14:77487799
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.142-2880C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487799 | ||||||
chr14:77487836
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142-2917G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487836 | ||||||
chr14:77487876
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(104): Show | 114 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.142-2957C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487876 | ||||||
chr14:77487938
|
G | C | 1 | a0002c0002t0001g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.142-3019C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487938 | ||||||
chr14:77487982
|
G | A | 1 | a0002c0002t0001g0081 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.142-3063C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487982 | ||||||
chr14:77488208
|
G | A | 2 | a0002c0002t0001g0058a0002c0002t0003g0201 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142-3289C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77488208 | ||||||
chr14:77488256
|
C | T | 1 | a0002c0002t0003g0122 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.142-3337G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77488256 | ||||||
chr14:77488510
|
T | C | 15 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0077others(12): Show | 19 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.142-3591A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77488510 | ||||||
chr14:77488693
|
C | T | 2 | a0002c0002t0005g0009a0002c0002t0005g0119 | 3 | HG01243.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.142-3774G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77488693 | ||||||
chr14:77488896
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.142-3977C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77488896 | ||||||
chr14:77489042
|
C | T | 1 | a0002c0002t0001g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.142-4123G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489042 | ||||||
chr14:77489084
|
C | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.142-4165G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489084 | ||||||
chr14:77489332
|
T | C | 1 | a0003c0004t0001g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-4413A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489332 | ||||||
chr14:77489416
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-4497A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489416 | ||||||
chr14:77489429
|
C | T | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142-4510G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489429 | ||||||
chr14:77489552
|
C | CT | 139 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.142-4634dupA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489552 | ||||||
chr14:77489719
|
A | G | 1 | a0008c0016t0003g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-4800T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489719 | ||||||
chr14:77489903
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.142-4984C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489903 | ||||||
chr14:77489948
|
A | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.142-5029T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489948 | ||||||
chr14:77489949
|
A | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.142-5030T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489949 | ||||||
chr14:77489965
|
G | A | 2 | a0005c0014t0001g0026a0005c0014t0001g0027 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142-5046C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489965 | ||||||
chr14:77489990
|
A | G | 1 | a0002c0002t0006g0195 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142-5071T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489990 | ||||||
chr14:77490009
|
G | A | 1 | a0002c0002t0001g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-5090C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490009 | ||||||
chr14:77490021
|
G | A | 4 | a0002c0002t0001g0001a0002c0002t0001g0077a0002c0002t0008g0075others(1): Show | 6 | HG01891.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-5102C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490021 | ||||||
chr14:77490064
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.142-5145G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490064 | ||||||
chr14:77490098
|
C | T | 1 | a0002c0002t0003g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.142-5179G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490098 | ||||||
chr14:77490110
|
T | TCCTCGGC others(127): Show |
1 | a0002c0002t0003g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.142-5192_142-5191i others(136): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490110 | ||||||
chr14:77490145
|
G | T | 1 | a0002c0002t0003g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.142-5226C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490145 | ||||||
chr14:77490149
|
C | T | 3 | a0002c0002t0003g0018a0002c0002t0003g0019a0002c0002t0011g0244 | 3 | HG02630.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142-5230G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490149 | ||||||
chr14:77490155
|
G | A | 3 | a0002c0002t0006g0065a0002c0002t0006g0079a0002c0002t0006g0195 | 3 | HG02922.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.142-5236C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490155 | ||||||
chr14:77490159
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.142-5240C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490159 | ||||||
chr14:77490199
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.142-5280T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490199 | ||||||
chr14:77490213
|
G | A | 3 | a0002c0002t0002g0071a0002c0002t0002g0164a0002c0002t0002g0167 | 3 | HG02738.hp2 HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.142-5294C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490213 | ||||||
chr14:77490222
|
C | CTCTTGAC others(7): Show |
1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142-5317_142-5304d others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490222 | ||||||
chr14:77490390
|
G | GAAAAGTA others(9): Show |
242 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(239): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.142-5472_142-5471i others(18): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490390 | ||||||
chr14:77490390
|
G | GAAAAGTA others(10): Show |
1 | a0001c0001t0001g0150 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.142-5472_142-5471i others(19): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490390 | ||||||
chr14:77490393
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.142-5474G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490393 | ||||||
chr14:77490434
|
T | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0145others(2): Show | 6 | HG01256.hp2 HG01361.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-5515A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490434 | ||||||
chr14:77490498
|
C | T | 14 | a0001c0001t0001g0069a0002c0002t0001g0066a0002c0002t0001g0067others(11): Show | 14 | HG00099.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.142-5579G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490498 | ||||||
chr14:77490518
|
T | A | 16 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(13): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-5599A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490518 | ||||||
chr14:77490520
|
A | T | 1 | a0002c0002t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.142-5601T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490520 | ||||||
chr14:77490622
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.142-5703C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490622 | ||||||
chr14:77490760
|
C | T | 3 | a0002c0002t0001g0058a0003c0004t0001g0197a0008c0016t0003g0205 | 3 | HG01123.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.142-5841G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490760 | ||||||
chr14:77491011
|
G | A | 55 | a0001c0001t0001g0069a0002c0002t0001g0058a0002c0002t0001g0066others(52): Show | 56 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.142-6092C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491011 | ||||||
chr14:77491034
|
G | A | 81 | a0001c0001t0001g0069a0002c0002t0001g0014a0002c0002t0001g0058others(78): Show | 85 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.142-6115C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491034 | ||||||
chr14:77491107
|
G | A | 2 | a0001c0001t0001g0199a0009c0019t0010g0207 | 2 | HG00621.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.142-6188C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491107 | ||||||
chr14:77491169
|
G | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.142-6250C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491169 | ||||||
chr14:77491170
|
G | A | 1 | a0003c0004t0001g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-6251C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491170 | ||||||
chr14:77491214
|
G | A | 2 | a0002c0002t0002g0206a0002c0002t0002g0211 | 2 | HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.142-6295C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491214 | ||||||
chr14:77491348
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.142-6429G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491348 | ||||||
chr14:77491390
|
T | G | 1 | a0001c0001t0001g0220 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.142-6471A>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491390 | ||||||
chr14:77491414
|
G | T | 6 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(3): Show | 7 | HG02109.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-6495C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491414 | ||||||
chr14:77491550
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.142-6631C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491550 | ||||||
chr14:77491590
|
C | T | 1 | a0002c0002t0002g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-6671G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491590 | ||||||
chr14:77491685
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.142-6766A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491685 | ||||||
chr14:77491685
|
T | G | 60 | a0001c0001t0001g0069a0002c0002t0001g0058a0002c0002t0001g0066others(57): Show | 61 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.142-6766A>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491685 | ||||||
chr14:77491691
|
C | CT | 30 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0102others(27): Show | 30 | HG00621.hp2 HG00735.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-6773dupA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491691 | ||||||
chr14:77491691
|
CT | C | 11 | a0001c0001t0001g0043a0001c0001t0001g0047a0002c0002t0001g0170others(8): Show | 11 | HG01123.hp2 HG01167.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-6773delA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491691 | ||||||
chr14:77491691
|
CTT | C | 18 | a0002c0002t0001g0014a0002c0002t0001g0245a0002c0002t0001g0246others(15): Show | 21 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.142-6774_142-6773d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491691 | ||||||
chr14:77491717
|
G | A | 16 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(13): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-6798C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491717 | ||||||
chr14:77491747
|
G | A | 1 | a0002c0002t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.142-6828C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491747 | ||||||
chr14:77491820
|
C | T | 1 | a0001c0001t0017g0114 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.141+6833G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491820 | ||||||
chr14:77491859
|
C | T | 52 | a0001c0001t0001g0069a0002c0002t0001g0066a0002c0002t0001g0067others(49): Show | 53 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.141+6794G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491859 | ||||||
chr14:77492000
|
C | CT | 23 | a0001c0001t0001g0063a0002c0002t0001g0014a0002c0002t0001g0245others(20): Show | 26 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+6652dupA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492000 | ||||||
chr14:77492013
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.141+6640A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492013 | ||||||
chr14:77492032
|
A | G | 57 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(54): Show | 61 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.141+6621T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492032 | ||||||
chr14:77492361
|
C | T | 21 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0016g0128others(18): Show | 23 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.141+6292G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492361 | ||||||
chr14:77492362
|
G | C | 1 | a0002c0007t0015g0059 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.141+6291C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492362 | ||||||
chr14:77492415
|
G | A | 2 | a0002c0007t0001g0020a0002c0007t0015g0059 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.141+6238C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492415 | ||||||
chr14:77492443
|
C | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0186 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.141+6210G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492443 | ||||||
chr14:77492472
|
G | A | 20 | a0001c0001t0001g0069a0002c0002t0001g0066a0002c0002t0001g0067others(17): Show | 20 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+6181C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492472 | ||||||
chr14:77492516
|
CT | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.141+6136delA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492516 | ||||||
chr14:77492516
|
CTT | C | 7 | a0001c0001t0001g0048a0002c0002t0001g0058a0002c0002t0001g0094others(4): Show | 7 | HG01123.hp2 HG02630.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+6135_141+6136d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492516 | ||||||
chr14:77492536
|
T | C | 1 | a0002c0021t0002g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.141+6117A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492536 | ||||||
chr14:77492580
|
T | C | 4 | a0002c0002t0001g0014a0002c0002t0001g0245a0002c0002t0001g0246others(1): Show | 5 | HG02451.hp1 HG02572.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+6073A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492580 | ||||||
chr14:77492605
|
G | A | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+6048C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492605 | ||||||
chr14:77492614
|
G | T | 16 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(13): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+6039C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492614 | ||||||
chr14:77492633
|
T | G | 1 | a0003c0004t0001g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.141+6020A>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492633 | ||||||
chr14:77492705
|
T | A | 14 | a0001c0001t0001g0056a0001c0001t0001g0146a0001c0001t0001g0147others(11): Show | 14 | HG00408.hp1 HG01981.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+5948A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492705 | ||||||
chr14:77492725
|
C | T | 16 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(13): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+5928G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492725 | ||||||
chr14:77492746
|
G | A | 1 | a0005c0014t0001g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.141+5907C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492746 | ||||||
chr14:77492766
|
G | C | 2 | a0002c0002t0001g0058a0008c0016t0003g0205 | 2 | HG01123.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.141+5887C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492766 | ||||||
chr14:77492781
|
A | G | 1 | a0002c0002t0006g0195 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.141+5872T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492781 | ||||||
chr14:77493017
|
A | G | 16 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(13): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+5636T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493017 | ||||||
chr14:77493147
|
C | T | 16 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(13): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+5506G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493147 | ||||||
chr14:77493344
|
T | C | 2 | a0002c0002t0001g0001a0002c0002t0001g0077 | 4 | HG02717.hp2 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+5309A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493344 | ||||||
chr14:77493380
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.141+5273A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493380 | ||||||
chr14:77493521
|
G | C | 1 | a0007c0011t0001g0133 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.141+5132C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493521 | ||||||
chr14:77493556
|
A | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.141+5097T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493556 | ||||||
chr14:77493595
|
G | A | 2 | a0002c0002t0001g0209a0002c0002t0001g0228 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.141+5058C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493595 | ||||||
chr14:77493762
|
G | A | 1 | a0002c0002t0002g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.141+4891C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493762 | ||||||
chr14:77493835
|
G | A | 1 | a0002c0002t0003g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.141+4818C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493835 | ||||||
chr14:77493875
|
C | T | 1 | a0002c0002t0002g0113 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.141+4778G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493875 | ||||||
chr14:77493876
|
G | A | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+4777C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493876 | ||||||
chr14:77493938
|
A | AT | 6 | a0001c0001t0001g0150a0002c0002t0001g0014a0002c0002t0001g0245others(3): Show | 7 | HG02451.hp1 HG02572.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+4714dupA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493938 | ||||||
chr14:77493979
|
G | A | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+4674C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493979 | ||||||
chr14:77493988
|
A | G | 1 | a0002c0007t0001g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+4665T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493988 | ||||||
chr14:77494024
|
G | A | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+4629C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494024 | ||||||
chr14:77494059
|
G | C | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+4594C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494059 | ||||||
chr14:77494716
|
C | T | 1 | a0002c0002t0006g0079 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.141+3937G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494716 | ||||||
chr14:77494745
|
G | A | 1 | a0009c0019t0010g0207 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.141+3908C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494745 | ||||||
chr14:77494826
|
T | C | 1 | a0003c0004t0001g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.141+3827A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494826 | ||||||
chr14:77494884
|
TTTTA | T | 16 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(13): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+3765_141+3768d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494884 | ||||||
chr14:77494916
|
C | T | 3 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0037 | 3 | HG00140.hp1 HG00642.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.141+3737G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494916 | ||||||
chr14:77495024
|
C | T | 15 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(12): Show | 17 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+3629G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495024 | ||||||
chr14:77495067
|
G | A | 1 | a0002c0007t0001g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+3586C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495067 | ||||||
chr14:77495120
|
G | C | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+3533C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495120 | ||||||
chr14:77495206
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | NA19065.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.141+3447C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495206 | ||||||
chr14:77495266
|
G | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.141+3387C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495266 | ||||||
chr14:77495669
|
G | A | 8 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(5): Show | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+2984C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495669 | ||||||
chr14:77495703
|
G | A | 15 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(12): Show | 17 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+2950C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495703 | ||||||
chr14:77495934
|
C | T | 1 | a0002c0002t0003g0202 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.141+2719G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495934 | ||||||
chr14:77496184
|
G | GT | 93 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0044others(90): Show | 101 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.141+2468_141+2469i others(3): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496184 | ||||||
chr14:77496185
|
C | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.141+2468G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496185 | ||||||
chr14:77496186
|
C | A | 93 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0044others(90): Show | 101 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.141+2467G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496186 | ||||||
chr14:77496247
|
G | T | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+2406C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496247 | ||||||
chr14:77496248
|
G | T | 1 | a0001c0001t0004g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.141+2405C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496248 | ||||||
chr14:77496298
|
GACCAACA others(7): Show |
G | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+2341_141+2354d others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496298 | ||||||
chr14:77496353
|
T | A | 3 | a0002c0003t0001g0254a0002c0003t0001g0255a0002c0003t0007g0260 | 3 | NA18946.hp2 NA18967.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.141+2300A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496353 | ||||||
chr14:77496381
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.141+2272C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496381 | ||||||
chr14:77496420
|
G | A | 20 | a0001c0001t0001g0069a0002c0002t0001g0066a0002c0002t0001g0067others(17): Show | 20 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+2233C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496420 | ||||||
chr14:77496594
|
C | A | 2 | a0002c0007t0001g0020a0002c0007t0015g0059 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.141+2059G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496594 | ||||||
chr14:77496660
|
G | T | 15 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(12): Show | 17 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+1993C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496660 | ||||||
chr14:77496751
|
T | C | 21 | a0002c0002t0001g0014a0002c0002t0001g0245a0002c0002t0001g0246others(18): Show | 24 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.141+1902A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496751 | ||||||
chr14:77496799
|
G | GA | 22 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0032others(19): Show | 23 | HG00140.hp2 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.141+1853dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
G | GAA | 14 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0037others(11): Show | 15 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+1852_141+1853d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
G | GAAA | 6 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG01361.hp2 HG02055.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+1851_141+1853d others(5): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
G | GAAAAAAA others(3): Show |
1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+1844_141+1853d others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
G | GAAAAAAA others(6): Show |
1 | a0001c0001t0004g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.141+1841_141+1853d others(15): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GA | G | 45 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0093others(42): Show | 46 | HG00099.hp1 HG00408.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.141+1853delT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAA | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(51): Show | 62 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+1852_141+1853d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAAA | G | 8 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0127others(5): Show | 8 | HG00544.hp1 HG01069.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+1851_141+1853d others(5): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAAAA | G | 9 | a0002c0002t0001g0001a0002c0002t0001g0058a0002c0002t0001g0077others(6): Show | 11 | HG00323.hp1 HG01070.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.141+1850_141+1853d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAAAAA | G | 9 | a0002c0002t0001g0081a0002c0002t0001g0107a0002c0002t0001g0108others(6): Show | 9 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.141+1849_141+1853d others(7): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAAAAAA | G | 25 | a0001c0001t0001g0234a0002c0002t0001g0070a0002c0002t0001g0084others(22): Show | 26 | HG01099.hp1 HG02071.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+1848_141+1853d others(8): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAAAAAAA | G | 23 | a0001c0001t0001g0069a0002c0002t0001g0066a0002c0002t0001g0067others(20): Show | 23 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.141+1847_141+1853d others(9): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0001g0126a0002c0002t0001g0189 | 2 | HG02071.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.141+1844_141+1853d others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAAAAAAA others(9): Show |
G | 1 | a0002c0003t0001g0251 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.141+1838_141+1853d others(18): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAAAAAAA others(10): Show |
G | 14 | a0002c0002t0008g0075a0002c0003t0001g0016a0002c0003t0001g0250others(11): Show | 16 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.141+1837_141+1853d others(19): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAAAAAAA others(11): Show |
G | 1 | a0002c0003t0001g0249 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.141+1836_141+1853d others(20): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496799
|
GAAAAAAA others(12): Show |
G | 2 | a0001c0009t0004g0072a0001c0009t0004g0088 | 2 | HG01109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+1835_141+1853d others(21): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | ||||||
chr14:77496804
|
A | G | 1 | a0002c0002t0001g0188 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.141+1849T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496804 | ||||||
chr14:77496929
|
A | C | 55 | a0001c0001t0001g0069a0002c0002t0001g0058a0002c0002t0001g0066others(52): Show | 56 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.141+1724T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496929 | ||||||
chr14:77496933
|
C | T | 2 | a0001c0001t0001g0172a0002c0002t0002g0113 | 2 | HG01081.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.141+1720G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496933 | ||||||
chr14:77497020
|
T | G | 1 | a0001c0001t0001g0225 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.141+1633A>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497020 | ||||||
chr14:77497045
|
C | G | 3 | a0001c0001t0004g0226a0001c0001t0004g0241a0001c0001t0004g0243 | 3 | HG02145.hp2 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.141+1608G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497045 | ||||||
chr14:77497351
|
C | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.141+1302G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497351 | ||||||
chr14:77497367
|
C | CA | 55 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(52): Show | 60 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.141+1285dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497367 | ||||||
chr14:77497367
|
C | CAA | 68 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0054others(65): Show | 72 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.141+1284_141+1285d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497367 | ||||||
chr14:77497367
|
C | CAAA | 9 | a0001c0001t0001g0106a0001c0001t0001g0148a0001c0001t0001g0150others(6): Show | 9 | HG01978.hp1 HG01978.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+1283_141+1285d others(5): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497367 | ||||||
chr14:77497367
|
CA | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 29 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.141+1285delT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497367 | ||||||
chr14:77497493
|
T | A | 1 | a0010c0022t0001g0248 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.141+1160A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497493 | ||||||
chr14:77497733
|
A | AGGAAGTA others(1): Show |
18 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(15): Show | 18 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.141+919_141+920ins others(8): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497733 | ||||||
chr14:77497733
|
AGGAAGGA others(5): Show |
A | 5 | a0002c0003t0001g0016a0002c0003t0001g0256a0002c0003t0001g0257others(2): Show | 6 | HG00741.hp1 HG01257.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+908_141+919del others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497733 | ||||||
chr14:77497733
|
AGGAAGGA others(9): Show |
A | 5 | a0002c0003t0001g0252a0002c0003t0001g0253a0002c0003t0001g0254others(2): Show | 6 | HG00642.hp1 HG00735.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+904_141+919del others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497733 | ||||||
chr14:77497737
|
A | AGGAGGGA others(1): Show |
5 | a0002c0002t0006g0195a0003c0004t0001g0197a0006c0013t0001g0112others(2): Show | 5 | HG03225.hp2 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+908_141+915dup others(8): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | ||||||
chr14:77497737
|
A | AGGAGGGA others(5): Show |
3 | a0002c0002t0001g0153a0002c0002t0001g0154a0002c0002t0002g0152 | 3 | HG02572.hp1 HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.141+904_141+915dup others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | ||||||
chr14:77497737
|
A | AGGAGGGA others(9): Show |
1 | a0002c0002t0001g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.141+900_141+915dup others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | ||||||
chr14:77497737
|
A | AGTAG | 24 | a0001c0001t0001g0005a0001c0001t0001g0212a0001c0001t0001g0213others(21): Show | 25 | HG00408.hp1 HG00621.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.141+915_141+916ins others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | ||||||
chr14:77497737
|
A | AGTAGGGA others(5): Show |
3 | a0001c0001t0001g0240a0001c0010t0007g0239a0002c0002t0002g0227 | 3 | HG03834.hp2 NA18990.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.141+915_141+916ins others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | ||||||
chr14:77497737
|
A | G | 6 | a0002c0002t0011g0244a0002c0003t0001g0249a0002c0003t0001g0250others(3): Show | 6 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+916T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | ||||||
chr14:77497739
|
G | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.141+914C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497739 | ||||||
chr14:77497741
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0212a0001c0001t0001g0213others(21): Show | 25 | HG00408.hp1 HG00621.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.141+912C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497741 | ||||||
chr14:77497745
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.141+908C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497745 | ||||||
chr14:77497749
|
GGGAGGGA others(17): Show |
G | 1 | a0002c0002t0001g0014 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.141+880_141+903del others(24): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497749 | ||||||
chr14:77497749
|
GGGAGGGA others(21): Show |
G | 3 | a0002c0002t0001g0245a0002c0002t0001g0246a0002c0002t0001g0247 | 3 | HG02897.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.141+876_141+903del others(28): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497749 | ||||||
chr14:77497756
|
A | T | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+897T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497756 | ||||||
chr14:77497757
|
GGGAGGGA others(13): Show |
G | 3 | a0002c0003t0001g0249a0002c0003t0001g0250a0002c0003t0001g0251 | 3 | HG01123.hp1 HG01255.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.141+876_141+895del others(20): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497757 | ||||||
chr14:77497757
|
GGGAGGGA others(21): Show |
G | 1 | a0010c0022t0001g0248 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.141+868_141+895del others(28): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497757 | ||||||
chr14:77497761
|
GGGAGGGA others(9): Show |
G | 3 | a0002c0002t0001g0151a0002c0002t0011g0244a0002c0007t0001g0020 | 3 | HG02559.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.141+876_141+891del others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497761 | ||||||
chr14:77497761
|
GGGAGGGA others(41): Show |
G | 8 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(5): Show | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+844_141+891del others(48): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497761 | ||||||
chr14:77497765
|
G | A | 3 | a0001c0001t0001g0240a0001c0001t0004g0241a0001c0010t0007g0239 | 3 | HG02145.hp2 NA18990.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.141+888C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497765 | ||||||
chr14:77497765
|
GGGAGGGA others(9): Show |
G | 1 | a0002c0002t0001g0110 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.141+872_141+887del others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497765 | ||||||
chr14:77497769
|
G | A | 20 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(17): Show | 20 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+884C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | ||||||
chr14:77497769
|
G | GGGAAGGA others(5): Show |
1 | a0001c0001t0004g0243 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.141+872_141+883dup others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | ||||||
chr14:77497769
|
G | GGGAGGGA others(9): Show |
1 | a0001c0001t0001g0242 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.141+883_141+884ins others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | ||||||
chr14:77497769
|
GGGAA | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.141+880_141+883del others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | ||||||
chr14:77497769
|
GGGAAGGA others(1): Show |
G | 39 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0089others(36): Show | 43 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.141+876_141+883del others(8): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | ||||||
chr14:77497769
|
GGGAAGGA others(5): Show |
G | 13 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0009t0004g0072others(10): Show | 15 | HG01167.hp2 HG01891.hp1 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+872_141+883del others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | ||||||
chr14:77497769
|
GGGAAGGA others(9): Show |
G | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG00099.hp2 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+868_141+883del others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | ||||||
chr14:77497769
|
GGGAAGGA others(17): Show |
G | 1 | a0002c0002t0003g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.141+860_141+883del others(24): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | ||||||
chr14:77497771
|
G | A | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+882C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497771 | ||||||
chr14:77497772
|
A | G | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+881T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497772 | ||||||
chr14:77497773
|
A | G | 70 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0039others(67): Show | 74 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.141+880T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497773 | ||||||
chr14:77497777
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(48): Show | 56 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.141+876T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497777 | ||||||
chr14:77497781
|
A | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0082others(30): Show | 35 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.141+872T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497781 | ||||||
chr14:77497782
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.141+871C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497782 | ||||||
chr14:77497785
|
A | G | 11 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0009t0004g0072others(8): Show | 13 | HG01167.hp2 HG01891.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.141+868T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497785 | ||||||
chr14:77497786
|
G | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0064 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.141+867C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497786 | ||||||
chr14:77497789
|
A | G | 6 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 6 | HG01099.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+864T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497789 | ||||||
chr14:77497794
|
G | A | 4 | a0002c0002t0003g0018a0002c0002t0003g0019a0002c0002t0011g0244others(1): Show | 4 | HG02630.hp2 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+859C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497794 | ||||||
chr14:77497832
|
A | G | 1 | a0002c0023t0012g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+821T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497832 | ||||||
chr14:77497834
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.141+819T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497834 | ||||||
chr14:77497973
|
T | A | 4 | a0002c0002t0001g0014a0002c0002t0001g0245a0002c0002t0001g0246others(1): Show | 5 | HG02451.hp1 HG02572.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+680A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497973 | ||||||
chr14:77498117
|
A | G | 2 | a0001c0001t0001g0054a0002c0007t0001g0055 | 2 | HG00544.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.141+536T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498117 | ||||||
chr14:77498157
|
C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(23): Show | 27 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.141+496G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498157 | ||||||
chr14:77498318
|
T | C | 15 | a0002c0003t0001g0016a0002c0003t0001g0249a0002c0003t0001g0250others(12): Show | 17 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+335A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498318 | ||||||
chr14:77498323
|
A | T | 8 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(5): Show | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+330T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498323 | ||||||
chr14:77498425
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.141+228G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498425 | ||||||
chr14:77498614
|
C | G | 3 | a0002c0002t0003g0018a0002c0002t0003g0019a0002c0007t0001g0020 | 3 | HG02630.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.141+39G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498614 | ||||||
chr14:77498643
|
C | T | 1 | a0002c0021t0002g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.141+10G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498643 |