geneid | 79840 |
---|---|
ensemblid | ENSG00000187736.14 |
hgncid | 25737 |
symbol | NHEJ1 |
name | non-homologous end joining factor 1 |
refseq_nuc | NM_024782.3 |
refseq_prot | NP_079058.1 |
ensembl_nuc | ENST00000356853.10 |
ensembl_prot | ENSP00000349313.5 |
mane_status | MANE Select |
chr | chr2 |
start | 219069357 |
end | 219160815 |
strand | - |
ver | v1.2 |
region | chr2:219069357-219160815 |
region5000 | chr2:219064357-219165815 |
regionname0 | NHEJ1_chr2_219069357_219160815 |
regionname5000 | NHEJ1_chr2_219064357_219165815 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 299 | 334 | 69 | 51 | 170 | 8 | 34 | 140 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0002 | 0/0 | 299 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0003 | 0/0 | 299 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0004 | 0/0 | 299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 900 | 333 | 68 | 51 | 170 | 8 | 34 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
c0002 | 0/0 | 900 | 12 | 12 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
c0003 | 0/0 | 900 | 3 | 2 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
c0004 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
c0005 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 7121 | 126 | 15 | 23 | 72 | 4 | 12 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0002 | 0/0 | 7121 | 65 | 17 | 8 | 29 | 2 | 9 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0003 | 0/0 | 7121 | 42 | 6 | 3 | 28 | 1 | 4 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0004 | 0/0 | 7121 | 12 | 0 | 0 | 12 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0005 | 0/1 | 7121 | 11 | 0 | 8 | 0 | 1 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0006 | 0/0 | 7121 | 11 | 11 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0007 | 0/0 | 7121 | 7 | 0 | 0 | 7 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0008 | 0/0 | 7193 | 6 | 6 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0009 | 0/0 | 7121 | 5 | 3 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0010 | 0/0 | 7121 | 4 | 1 | 0 | 3 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0011 | 0/0 | 7121 | 4 | 4 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0012 | 0/0 | 7122 | 4 | 4 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0013 | 0/0 | 7121 | 3 | 3 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0014 | 0/0 | 7121 | 3 | 0 | 0 | 3 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0015 | 0/0 | 7121 | 3 | 0 | 0 | 3 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0016 | 0/0 | 7120 | 3 | 3 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0017 | 0/0 | 7121 | 2 | 0 | 0 | 2 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0018 | 0/0 | 7120 | 2 | 0 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0019 | 0/0 | 7121 | 2 | 0 | 0 | 0 | 0 | 2 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0020 | 0/0 | 7121 | 2 | 0 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0021 | 0/0 | 7121 | 2 | 0 | 1 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0022 | 1/0 | 7121 | 2 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0023 | 0/0 | 7121 | 2 | 2 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0024 | 0/0 | 7121 | 2 | 2 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0025 | 0/0 | 7121 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0026 | 0/0 | 7120 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0027 | 0/0 | 7121 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0028 | 0/0 | 7121 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0029 | 0/0 | 7121 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0030 | 0/0 | 7120 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0031 | 0/0 | 7121 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0032 | 0/0 | 7121 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0033 | 0/0 | 7121 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0034 | 0/0 | 7122 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0035 | 0/0 | 7120 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0036 | 0/0 | 7121 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0037 | 0/0 | 7121 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0038 | 0/0 | 7121 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0039 | 0/0 | 7121 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0040 | 0/0 | 7121 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0041 | 0/0 | 7121 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0042 | 0/0 | 7121 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0043 | 0/0 | 7121 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0044 | 0/0 | 7122 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0045 | 0/0 | 7121 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0046 | 0/0 | 7122 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0047 | 0/0 | 7121 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0048 | 0/0 | 7121 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
t0049 | 0/0 | 7122 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 900 | 333 | 68 | 51 | 170 | 8 | 34 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0004 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0002c0002 | 0/0 | 900 | 12 | 12 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0003c0003 | 0/0 | 900 | 3 | 2 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0004c0005 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8020 | 125 | 14 | 23 | 72 | 4 | 12 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0002 | 0/0 | 8020 | 65 | 17 | 8 | 29 | 2 | 9 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0003 | 0/0 | 8020 | 42 | 6 | 3 | 28 | 1 | 4 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0004 | 0/0 | 8020 | 12 | 0 | 0 | 12 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0005 | 0/1 | 8020 | 11 | 0 | 8 | 0 | 1 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0006 | 0/0 | 8020 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0007 | 0/0 | 8020 | 7 | 0 | 0 | 7 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0008 | 0/0 | 8092 | 6 | 6 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0009 | 0/0 | 8020 | 2 | 1 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0010 | 0/0 | 8020 | 4 | 1 | 0 | 3 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0011 | 0/0 | 8020 | 4 | 4 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0012 | 0/0 | 8021 | 4 | 4 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0013 | 0/0 | 8020 | 3 | 3 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0014 | 0/0 | 8020 | 3 | 0 | 0 | 3 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0015 | 0/0 | 8020 | 3 | 0 | 0 | 3 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0016 | 0/0 | 8019 | 2 | 2 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0017 | 0/0 | 8020 | 2 | 0 | 0 | 2 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0018 | 0/0 | 8019 | 2 | 0 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0019 | 0/0 | 8020 | 2 | 0 | 0 | 0 | 0 | 2 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0020 | 0/0 | 8020 | 2 | 0 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0021 | 0/0 | 8020 | 2 | 0 | 1 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0022 | 1/0 | 8020 | 2 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0023 | 0/0 | 8020 | 2 | 2 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0025 | 0/0 | 8020 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0026 | 0/0 | 8019 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0027 | 0/0 | 8020 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0028 | 0/0 | 8020 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0029 | 0/0 | 8020 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0030 | 0/0 | 8019 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0031 | 0/0 | 8020 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0032 | 0/0 | 8020 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0033 | 0/0 | 8020 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0034 | 0/0 | 8021 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0035 | 0/0 | 8019 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0036 | 0/0 | 8020 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0037 | 0/0 | 8020 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0038 | 0/0 | 8020 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0039 | 0/0 | 8020 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0040 | 0/0 | 8020 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0041 | 0/0 | 8020 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0042 | 0/0 | 8020 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0043 | 0/0 | 8020 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0044 | 0/0 | 8021 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0045 | 0/0 | 8020 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0046 | 0/0 | 8021 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0047 | 0/0 | 8020 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0048 | 0/0 | 8020 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0001t0049 | 0/0 | 8021 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0001c0004t0001 | 0/0 | 8020 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0002c0002t0006 | 0/0 | 8020 | 10 | 10 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0002c0002t0024 | 0/0 | 8020 | 2 | 2 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0003c0003t0009 | 0/0 | 8020 | 3 | 2 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
a0004c0005t0016 | 0/0 | 8019 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | copy fasta | chr2 | 219064357 | 219165815 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0007g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0007g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0007g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0009g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0009g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0010g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0010g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0010g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0011g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0011g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0011g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0012g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0012g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0013g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0013g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0013g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0014g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0014g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0014g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0015g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0015g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0015g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0016g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0016g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0017g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0017g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0018g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0018g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0019g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0019g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0020g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0020g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0021g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0021g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0022g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0022g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0023g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0023g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0025g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0026g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0027g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0028g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0029g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0030g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0031g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0032g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0033g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0034g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0035g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0036g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0037g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0038g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0039g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0040g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0041g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0042g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0043g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0044g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0045g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0046g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0047g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0048g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0001t0049g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0001c0004t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0024g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0002c0002t0024g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0003c0003t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0003c0003t0009g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0003c0003t0009g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
a0004c0005t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | GBR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0097 | EUR | GBR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00544 | hp2 | a0001 | c0001 | t0038 | g0156 | EAS | CHS | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | CHS | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00609 | hp1 | a0001 | c0001 | t0036 | g0077 | EAS | CHS | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00642 | hp2 | a0001 | c0001 | t0018 | g0220 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0090 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01169 | hp2 | a0001 | c0001 | t0026 | g0167 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01175 | hp2 | a0001 | c0001 | t0009 | g0326 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0055 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0166 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01261 | hp1 | a0001 | c0001 | t0020 | g0224 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01346 | hp2 | a0001 | c0001 | t0033 | g0079 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01361 | hp1 | a0001 | c0001 | t0018 | g0219 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01361 | hp2 | a0001 | c0001 | t0020 | g0223 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01884 | hp2 | a0002 | c0002 | t0006 | g0149 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0140 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01975 | hp1 | a0003 | c0003 | t0009 | g0323 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0338 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02015 | hp2 | a0001 | c0001 | t0014 | g0085 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02055 | hp2 | a0001 | c0001 | t0008 | g0141 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02071 | hp2 | a0001 | c0001 | t0010 | g0334 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02083 | hp1 | a0001 | c0001 | t0010 | g0335 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02132 | hp2 | a0001 | c0001 | t0007 | g0062 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02145 | hp1 | a0001 | c0001 | t0046 | g0159 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CDX | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | CDX | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02257 | hp2 | a0002 | c0002 | t0006 | g0151 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02258 | hp1 | a0002 | c0002 | t0006 | g0150 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02273 | hp1 | a0001 | c0001 | t0042 | g0114 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02280 | hp1 | a0001 | c0001 | t0044 | g0154 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02293 | hp1 | a0001 | c0001 | t0021 | g0170 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02451 | hp2 | a0002 | c0002 | t0006 | g0148 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02615 | hp1 | a0002 | c0002 | t0006 | g0125 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02615 | hp2 | a0001 | c0001 | t0012 | g0117 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02622 | hp1 | a0001 | c0001 | t0047 | g0328 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02630 | hp1 | a0001 | c0001 | t0011 | g0332 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02630 | hp2 | a0002 | c0002 | t0024 | g0129 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02647 | hp1 | a0002 | c0002 | t0006 | g0146 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02647 | hp2 | a0001 | c0001 | t0023 | g0152 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02717 | hp2 | a0001 | c0001 | t0034 | g0139 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02738 | hp2 | a0001 | c0001 | t0019 | g0243 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02886 | hp1 | a0001 | c0001 | t0012 | g0002 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02886 | hp2 | a0001 | c0004 | t0001 | g0155 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02896 | hp2 | a0001 | c0001 | t0008 | g0142 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0143 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0002 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03017 | hp1 | a0001 | c0001 | t0022 | g0221 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0144 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03130 | hp1 | a0001 | c0001 | t0013 | g0131 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03139 | hp2 | a0004 | c0005 | t0016 | g0123 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03209 | hp2 | a0003 | c0003 | t0009 | g0322 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03486 | hp1 | a0001 | c0001 | t0039 | g0130 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03492 | hp1 | a0001 | c0001 | t0037 | g0072 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0145 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ESN | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03540 | hp1 | a0001 | c0001 | t0048 | g0028 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03540 | hp2 | a0002 | c0002 | t0006 | g0147 | AFR | GWD | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03579 | hp1 | a0001 | c0001 | t0023 | g0153 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03579 | hp2 | a0003 | c0003 | t0009 | g0324 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | STU | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | STU | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03831 | hp2 | a0001 | c0001 | t0032 | g0198 | SAS | BEB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03834 | hp1 | a0001 | c0001 | t0029 | g0203 | SAS | BEB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | BEB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | STU | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | STU | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0042 | SAS | STU | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG04204 | hp2 | a0001 | c0001 | t0019 | g0217 | SAS | STU | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG04228 | hp1 | a0001 | c0001 | t0041 | g0056 | SAS | STU | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG04228 | hp2 | a0001 | c0001 | t0031 | g0310 | SAS | STU | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18522 | hp1 | a0002 | c0002 | t0024 | g0128 | AFR | YRI | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18522 | hp2 | a0001 | c0001 | t0016 | g0105 | AFR | YRI | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | CHB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | CHB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18943 | hp2 | a0001 | c0001 | t0025 | g0010 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18950 | hp2 | a0001 | c0001 | t0040 | g0048 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18964 | hp2 | a0001 | c0001 | t0007 | g0317 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18965 | hp1 | a0001 | c0001 | t0014 | g0076 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18969 | hp1 | a0001 | c0001 | t0035 | g0083 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18970 | hp2 | a0001 | c0001 | t0015 | g0175 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18977 | hp2 | a0001 | c0001 | t0045 | g0200 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18978 | hp2 | a0001 | c0001 | t0007 | g0122 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18979 | hp2 | a0001 | c0001 | t0007 | g0071 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18985 | hp1 | a0001 | c0001 | t0015 | g0339 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18986 | hp2 | a0001 | c0001 | t0028 | g0250 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18989 | hp2 | a0001 | c0001 | t0021 | g0169 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18991 | hp1 | a0001 | c0001 | t0027 | g0211 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18992 | hp1 | a0001 | c0001 | t0017 | g0009 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19002 | hp2 | a0001 | c0001 | t0010 | g0333 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19005 | hp1 | a0001 | c0001 | t0007 | g0316 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19006 | hp2 | a0001 | c0001 | t0043 | g0044 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19030 | hp1 | a0001 | c0001 | t0016 | g0104 | AFR | LWK | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19030 | hp2 | a0001 | c0001 | t0013 | g0341 | AFR | LWK | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0342 | AFR | LWK | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | LWK | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19055 | hp2 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19062 | hp1 | a0001 | c0001 | t0014 | g0086 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19074 | hp2 | a0001 | c0001 | t0017 | g0008 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19076 | hp1 | a0001 | c0001 | t0030 | g0296 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19082 | hp1 | a0001 | c0001 | t0015 | g0180 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19240 | hp1 | a0001 | c0001 | t0011 | g0330 | AFR | YRI | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | YRI | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA20129 | hp1 | a0002 | c0002 | t0006 | g0127 | AFR | ASW | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0161 | AFR | ASW | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0165 | EUR | TSI | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0068 | EUR | TSI | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | GIH | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | GIH | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0160 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02109 | hp2 | a0001 | c0001 | t0011 | g0331 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02486 | hp2 | a0002 | c0002 | t0006 | g0126 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG02559 | hp2 | a0001 | c0001 | t0011 | g0069 | AFR | ACB | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03471 | hp1 | a0002 | c0002 | t0006 | g0124 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | MSL | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | USA | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | USA | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA18955 | hp2 | a0001 | c0001 | t0007 | g0290 | EAS | JPT | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | USA | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0327 | AFR | USA | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA21309 | hp1 | a0001 | c0001 | t0049 | g0343 | AFR | LWK | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | LWK | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0032 | REF | REF | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0022 | g0135 | REF | REF | NHEJ1_chr2_219064357_219165815 | NHEJ1 | chr2 | 219064357 | 219165815 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:219077304
|
T | A | 1 | a0003 | 3 | HG01975.hp1 HG03209.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.767A>T | p.Gln256Leu | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/8 | 863/8020 | 767/900 | 256/299 | chr2 | 219077304 | ||
chr2:219157586
|
T | G | 1 | a0004 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.276A>C | p.Glu92Asp | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/8 | 372/8020 | 276/900 | 92/299 | chr2 | 219157586 | ||
chr2:219158323
|
C | T | 1 | a0002 | 12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
missense_variant | MODERATE | c.40G>A | p.Ala14Thr | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/8 | 136/8020 | 40/900 | 14/299 | chr2 | 219158323 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:219147735
|
T | G | 1 | a0001c0004 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.451A>C | p.Arg151Arg | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 4/8 | 547/8020 | 451/900 | 151/299 | chr2 | 219147735 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:219069426
|
G | A | 1 | a0001c0001t0015 | 3 | NA18970.hp2 NA18985.hp1 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6955C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 6955 | chr2 | 219069426 | |||||
chr2:219069626
|
G | T | 15 | a0001c0001t0003a0001c0001t0010a0001c0001t0012others(12): Show | 66 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*6755C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 6755 | chr2 | 219069626 | |||||
chr2:219069755
|
C | T | 1 | a0001c0001t0027 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6626G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 6626 | chr2 | 219069755 | |||||
chr2:219069868
|
G | A | 1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6513C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 6513 | chr2 | 219069868 | |||||
chr2:219070187
|
T | A | 1 | a0001c0001t0037 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6194A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 6194 | chr2 | 219070187 | |||||
chr2:219070331
|
A | G | 1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6050T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 6050 | chr2 | 219070331 | |||||
chr2:219070340
|
C | A | 1 | a0001c0001t0032 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6041G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 6041 | chr2 | 219070340 | |||||
chr2:219070341
|
G | A | 1 | a0001c0001t0036 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6040C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 6040 | chr2 | 219070341 | |||||
chr2:219070400
|
C | G | 1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5981G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 5981 | chr2 | 219070400 | |||||
chr2:219070683
|
T | C | 1 | a0001c0001t0043 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5698A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 5698 | chr2 | 219070683 | |||||
chr2:219070817
|
C | T | 1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5564G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 5564 | chr2 | 219070817 | |||||
chr2:219070973
|
C | T | 2 | a0001c0001t0026a0001c0001t0029 | 2 | HG01169.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5408G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 5408 | chr2 | 219070973 | |||||
chr2:219070997
|
C | T | 1 | a0001c0001t0013 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5384G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 5384 | chr2 | 219070997 | |||||
chr2:219070998
|
G | C | 1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5383C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 5383 | chr2 | 219070998 | |||||
chr2:219071038
|
C | G | 1 | a0001c0001t0023 | 2 | HG02647.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5343G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 5343 | chr2 | 219071038 | |||||
chr2:219071112
|
C | A | 1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5269G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 5269 | chr2 | 219071112 | |||||
chr2:219071350
|
G | C | 1 | a0001c0001t0028 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5031C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 5031 | chr2 | 219071350 | |||||
chr2:219071436
|
C | T | 1 | a0001c0001t0046 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4945G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 4945 | chr2 | 219071436 | |||||
chr2:219071592
|
A | G | 1 | a0001c0001t0047 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4789T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 4789 | chr2 | 219071592 | |||||
chr2:219071748
|
C | T | 1 | a0001c0001t0011 | 4 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4633G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 4633 | chr2 | 219071748 | |||||
chr2:219071772
|
C | T | 7 | a0001c0001t0003a0001c0001t0010a0001c0001t0015others(4): Show | 54 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*4609G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 4609 | chr2 | 219071772 | |||||
chr2:219071867
|
T | C | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(13): Show | 110 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*4514A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 4514 | chr2 | 219071867 | |||||
chr2:219071901
|
AG | A | 2 | a0001c0001t0016a0004c0005t0016 | 3 | HG03139.hp2 NA18522.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4479delC | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 4479 | chr2 | 219071901 | |||||
chr2:219071908
|
T | A | 4 | a0001c0001t0012a0001c0001t0046a0001c0001t0047others(1): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4473A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 4473 | chr2 | 219071908 | |||||
chr2:219072149
|
C | T | 9 | a0001c0001t0003a0001c0001t0010a0001c0001t0015others(6): Show | 57 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*4232G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 4232 | chr2 | 219072149 | |||||
chr2:219072217
|
C | T | 4 | a0001c0001t0004a0001c0001t0014a0001c0001t0035others(1): Show | 17 | HG00609.hp1 HG02015.hp2 HG02074.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4164G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 4164 | chr2 | 219072217 | |||||
chr2:219072465
|
T | C | 1 | a0001c0001t0040 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3916A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 3916 | chr2 | 219072465 | |||||
chr2:219072504
|
T | C | 2 | a0001c0001t0026a0001c0001t0029 | 2 | HG01169.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3877A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 3877 | chr2 | 219072504 | |||||
chr2:219072579
|
T | C | 1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3802A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 3802 | chr2 | 219072579 | |||||
chr2:219072653
|
G | GAAAACAG others(66): Show |
1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3727_*3728insTTTT others(69): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 3727 | chr2 | 219072653 | |||||
chr2:219072792
|
C | T | 1 | a0001c0001t0038 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3589G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 3589 | chr2 | 219072792 | |||||
chr2:219072869
|
T | C | 1 | a0001c0001t0013 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3512A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 3512 | chr2 | 219072869 | |||||
chr2:219073282
|
G | A | 4 | a0001c0001t0005a0001c0001t0037a0001c0001t0041others(1): Show | 14 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3099C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 3099 | chr2 | 219073282 | |||||
chr2:219073334
|
T | C | 2 | a0001c0001t0009a0003c0003t0009 | 5 | HG01175.hp2 HG01975.hp1 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3047A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 3047 | chr2 | 219073334 | |||||
chr2:219073548
|
C | T | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(5): Show | 37 | HG00609.hp1 HG00639.hp2 HG00733.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2833G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 2833 | chr2 | 219073548 | |||||
chr2:219073817
|
G | T | 1 | a0001c0001t0021 | 2 | HG02293.hp1 NA18989.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2564C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 2564 | chr2 | 219073817 | |||||
chr2:219074014
|
A | T | 1 | a0001c0001t0043 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2367T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 2367 | chr2 | 219074014 | |||||
chr2:219074023
|
C | A | 1 | a0001c0001t0043 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2358G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 2358 | chr2 | 219074023 | |||||
chr2:219074048
|
G | C | 1 | a0001c0001t0020 | 2 | HG01261.hp1 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2333C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 2333 | chr2 | 219074048 | |||||
chr2:219074109
|
A | G | 1 | a0001c0001t0019 | 2 | HG02738.hp2 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2272T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 2272 | chr2 | 219074109 | |||||
chr2:219074296
|
T | C | 3 | a0001c0001t0006a0002c0002t0006a0002c0002t0024 | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2085A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 2085 | chr2 | 219074296 | |||||
chr2:219074447
|
A | G | 1 | a0001c0001t0014 | 3 | HG02015.hp2 NA18965.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1934T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1934 | chr2 | 219074447 | |||||
chr2:219074483
|
C | T | 2 | a0001c0001t0034a0001c0001t0044 | 2 | HG02280.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1898G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1898 | chr2 | 219074483 | |||||
chr2:219074613
|
A | G | 1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1768T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1768 | chr2 | 219074613 | |||||
chr2:219074717
|
A | G | 1 | a0001c0001t0008 | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1664T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1664 | chr2 | 219074717 | |||||
chr2:219074740
|
T | TA | 5 | a0001c0001t0012a0001c0001t0034a0001c0001t0044others(2): Show | 8 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1640dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1640 | chr2 | 219074740 | |||||
chr2:219074740
|
TA | T | 5 | a0001c0001t0008a0001c0001t0018a0001c0001t0026others(2): Show | 11 | HG00642.hp2 HG01169.hp2 HG01361.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1640delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1640 | chr2 | 219074740 | |||||
chr2:219074759
|
C | A | 1 | a0001c0001t0042 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1622G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1622 | chr2 | 219074759 | |||||
chr2:219074900
|
G | A | 1 | a0001c0001t0030 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1481 | chr2 | 219074900 | |||||
chr2:219074905
|
G | A | 1 | a0001c0001t0043 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1476C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1476 | chr2 | 219074905 | |||||
chr2:219074982
|
G | A | 1 | a0001c0001t0047 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1399C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1399 | chr2 | 219074982 | |||||
chr2:219075143
|
T | C | 1 | a0001c0001t0031 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1238A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1238 | chr2 | 219075143 | |||||
chr2:219075379
|
T | G | 1 | a0001c0001t0044 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1002A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 1002 | chr2 | 219075379 | |||||
chr2:219075396
|
C | T | 1 | a0001c0001t0010 | 4 | HG02071.hp2 HG02083.hp1 NA19002.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*985G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 985 | chr2 | 219075396 | |||||
chr2:219075665
|
T | C | 1 | a0001c0001t0045 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 716 | chr2 | 219075665 | |||||
chr2:219075762
|
C | T | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*619G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 619 | chr2 | 219075762 | |||||
chr2:219075898
|
A | G | 1 | a0001c0001t0034 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 483 | chr2 | 219075898 | |||||
chr2:219076052
|
C | T | 1 | a0001c0001t0013 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*329G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 329 | chr2 | 219076052 | |||||
chr2:219076110
|
A | G | 1 | a0001c0001t0033 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*271T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 271 | chr2 | 219076110 | |||||
chr2:219076224
|
G | A | 4 | a0001c0001t0012a0001c0001t0046a0001c0001t0047others(1): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*157C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 157 | chr2 | 219076224 | |||||
chr2:219076256
|
G | A | 1 | a0001c0001t0048 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 125 | chr2 | 219076256 | |||||
chr2:219076308
|
T | C | 1 | a0002c0002t0024 | 2 | HG02630.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*73A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 73 | chr2 | 219076308 | |||||
chr2:219076341
|
G | A | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 202 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*40C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 8/8 | 40 | chr2 | 219076341 | |||||
chr2:219160778
|
C | T | 1 | a0001c0001t0025 | 1 | NA18943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/8 | 2416 | chr2 | 219160778 | |||||
chr2:219160807
|
G | A | 1 | a0001c0001t0049 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-88C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/8 | 2445 | chr2 | 219160807 | |||||
chr2:219160810
|
G | T | 1 | a0001c0001t0017 | 2 | NA18992.hp1 NA19074.hp2 |
5_prime_UTR_variant | MODIFIER | c.-91C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/8 | 2448 | chr2 | 219160810 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:219076468
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.826-13C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076468 | ||||||
chr2:219076505
|
G | A | 5 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(2): Show | 6 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-50C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076505 | ||||||
chr2:219076513
|
G | A | 1 | a0001c0001t0005g0020 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.826-58C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076513 | ||||||
chr2:219076555
|
G | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-100C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076555 | ||||||
chr2:219076557
|
C | CT | 43 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0208others(40): Show | 43 | HG00741.hp2 HG01123.hp1 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.826-103dupA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076557 | ||||||
chr2:219076557
|
CT | C | 5 | a0001c0001t0001g0228a0001c0001t0001g0258a0001c0001t0001g0307others(2): Show | 6 | HG00673.hp2 HG01928.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-103delA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076557 | ||||||
chr2:219076557
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-112_826-103del others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076557 | ||||||
chr2:219076642
|
C | A | 5 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(2): Show | 6 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-187G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076642 | ||||||
chr2:219076795
|
C | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-340G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076795 | ||||||
chr2:219076864
|
G | A | 130 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(127): Show | 130 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.825+382C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076864 | ||||||
chr2:219076919
|
T | C | 2 | a0001c0001t0002g0027a0001c0001t0002g0029 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.825+327A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076919 | ||||||
chr2:219076933
|
A | AGATT | 13 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(10): Show | 13 | HG00408.hp2 NA18941.hp1 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.825+309_825+312dup others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076933 | ||||||
chr2:219076938
|
C | T | 1 | a0001c0001t0043g0044 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.825+308G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076938 | ||||||
chr2:219076956
|
T | C | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.825+290A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219076956 | ||||||
chr2:219077038
|
G | A | 1 | a0001c0001t0035g0083 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.825+208C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219077038 | ||||||
chr2:219077145
|
T | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.825+101A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219077145 | ||||||
chr2:219077217
|
C | T | 2 | a0001c0001t0005g0055a0001c0001t0041g0056 | 2 | HG01192.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.825+29G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 7/7 | chr2 | 219077217 | ||||||
chr2:219077371
|
T | A | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | splice_region_variant&intron_variant | LOW | c.707-7A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 6/7 | chr2 | 219077371 | ||||||
chr2:219077386
|
G | C | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.707-22C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 6/7 | chr2 | 219077386 | ||||||
chr2:219077391
|
T | C | 2 | a0001c0001t0034g0139a0001c0001t0044g0154 | 2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.707-27A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 6/7 | chr2 | 219077391 | ||||||
chr2:219077626
|
C | G | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.707-262G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 6/7 | chr2 | 219077626 | ||||||
chr2:219077650
|
A | AT | 59 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(56): Show | 64 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.707-287dupA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 6/7 | chr2 | 219077650 | ||||||
chr2:219077767
|
C | T | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.706+322G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 6/7 | chr2 | 219077767 | ||||||
chr2:219078082
|
G | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.706+7C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 6/7 | chr2 | 219078082 | ||||||
chr2:219078259
|
G | A | 6 | a0001c0001t0001g0225a0001c0001t0001g0229a0001c0001t0001g0241others(3): Show | 6 | HG00741.hp1 HG01258.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-53C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219078259 | ||||||
chr2:219078283
|
C | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-77G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219078283 | ||||||
chr2:219078285
|
GC | G | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-80delG | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219078285 | ||||||
chr2:219078354
|
G | A | 1 | a0001c0001t0003g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589-148C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219078354 | ||||||
chr2:219078410
|
A | G | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-204T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219078410 | ||||||
chr2:219078836
|
G | GT | 40 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(37): Show | 44 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.589-631dupA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219078836 | ||||||
chr2:219078846
|
C | G | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-640G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219078846 | ||||||
chr2:219079026
|
A | G | 1 | a0002c0002t0006g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.589-820T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079026 | ||||||
chr2:219079079
|
A | G | 55 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(52): Show | 59 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.589-873T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079079 | ||||||
chr2:219079106
|
T | A | 11 | a0001c0001t0002g0027a0001c0001t0002g0029a0001c0001t0002g0073others(8): Show | 11 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.589-900A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079106 | ||||||
chr2:219079124
|
G | A | 55 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(52): Show | 59 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.589-918C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079124 | ||||||
chr2:219079141
|
A | C | 2 | a0001c0001t0026g0167a0001c0001t0029g0203 | 2 | HG01169.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.589-935T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079141 | ||||||
chr2:219079251
|
CCTAGGCG others(14): Show |
C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-1066_589-1046d others(23): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079251 | ||||||
chr2:219079258
|
G | A | 1 | a0001c0001t0001g0007 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.589-1052C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079258 | ||||||
chr2:219079297
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.589-1091G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079297 | ||||||
chr2:219079313
|
C | T | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.589-1107G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079313 | ||||||
chr2:219079413
|
C | T | 53 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(50): Show | 57 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.589-1207G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079413 | ||||||
chr2:219079604
|
C | T | 1 | a0001c0001t0005g0165 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.589-1398G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079604 | ||||||
chr2:219079751
|
C | A | 2 | a0001c0001t0009g0326a0001c0001t0009g0327 | 2 | HG01175.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.589-1545G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079751 | ||||||
chr2:219079768
|
G | T | 1 | a0001c0001t0029g0203 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.589-1562C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079768 | ||||||
chr2:219079890
|
T | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-1684A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219079890 | ||||||
chr2:219080123
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.589-1917C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080123 | ||||||
chr2:219080185
|
A | ACTAT | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-1983_589-1980d others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080185 | ||||||
chr2:219080231
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.589-2025C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080231 | ||||||
chr2:219080237
|
T | G | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.589-2031A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080237 | ||||||
chr2:219080333
|
G | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2127C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080333 | ||||||
chr2:219080350
|
G | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2144C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080350 | ||||||
chr2:219080481
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0227others(5): Show | 10 | HG00639.hp1 HG01106.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.589-2275G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080481 | ||||||
chr2:219080530
|
A | T | 4 | a0001c0001t0001g0300a0001c0001t0002g0097a0001c0001t0007g0316others(1): Show | 4 | HG00099.hp2 NA18964.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-2324T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080530 | ||||||
chr2:219080534
|
T | A | 3 | a0001c0001t0001g0315a0001c0001t0002g0063a0001c0001t0047g0328 | 3 | HG02622.hp1 HG03654.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.589-2328A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080534 | ||||||
chr2:219080538
|
T | A | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.589-2332A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080538 | ||||||
chr2:219080548
|
A | AAT | 4 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-2343_589-2342i others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080548 | ||||||
chr2:219080550
|
A | AAT | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0017g0009 | 3 | HG01243.hp1 HG01884.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.589-2346_589-2345d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080550 | ||||||
chr2:219080550
|
A | T | 17 | a0001c0001t0001g0226a0001c0001t0001g0315a0001c0001t0002g0038others(14): Show | 17 | HG00733.hp2 HG01106.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.589-2344T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080550 | ||||||
chr2:219080550
|
AAT | A | 22 | a0001c0001t0001g0134a0001c0001t0001g0240a0001c0001t0001g0262others(19): Show | 22 | HG01175.hp2 HG01975.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.589-2346_589-2345d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080550 | ||||||
chr2:219080552
|
T | A | 137 | a0001c0001t0001g0315a0001c0001t0002g0023a0001c0001t0002g0026others(134): Show | 138 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.589-2346A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080552 | ||||||
chr2:219080554
|
T | A | 24 | a0001c0001t0002g0029a0001c0001t0002g0050a0001c0001t0002g0096others(21): Show | 24 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.589-2348A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080554 | ||||||
chr2:219080556
|
T | A | 1 | a0001c0001t0005g0165 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.589-2350A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080556 | ||||||
chr2:219080587
|
T | TTA | 13 | a0001c0001t0006g0098a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.589-2383_589-2382d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080587 | ||||||
chr2:219080588
|
T | A | 55 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(52): Show | 59 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.589-2382A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080588 | ||||||
chr2:219080589
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589-2409_589-2384d others(28): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080589 | ||||||
chr2:219080589
|
ATATATAT others(19): Show |
A | 36 | a0001c0001t0001g0084a0001c0001t0001g0162a0001c0001t0001g0182others(33): Show | 36 | HG00099.hp1 HG00642.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.589-2409_589-2384d others(28): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080589 | ||||||
chr2:219080589
|
ATATATAT others(45): Show |
A | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.589-2435_589-2384d others(54): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080589 | ||||||
chr2:219080598
|
T | A | 55 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(52): Show | 59 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.589-2392A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080598 | ||||||
chr2:219080604
|
T | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2398A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080604 | ||||||
chr2:219080615
|
T | TTA | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2411_589-2410d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080615 | ||||||
chr2:219080617
|
ATATATAT others(17): Show |
A | 2 | a0001c0001t0019g0217a0001c0001t0019g0243 | 2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.589-2435_589-2412d others(26): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080617 | ||||||
chr2:219080630
|
T | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2424A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080630 | ||||||
chr2:219080640
|
CTTATATA others(21): Show |
C | 71 | a0001c0001t0002g0027a0001c0001t0002g0029a0001c0001t0002g0073others(68): Show | 75 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.589-2462_589-2435d others(30): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080640 | ||||||
chr2:219080656
|
T | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2450A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080656 | ||||||
chr2:219080666
|
CTT | C | 19 | a0001c0001t0002g0063a0001c0001t0006g0098a0001c0001t0012g0002others(16): Show | 20 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.589-2462_589-2461d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080666 | ||||||
chr2:219080668
|
T | TATATATA others(355): Show |
1 | a0001c0001t0008g0145 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589-2463_589-2462i others(364): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080668 | ||||||
chr2:219080668
|
T | TATATATA others(303): Show |
5 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-2463_589-2462i others(312): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080668 | ||||||
chr2:219080668
|
T | TATATATA others(17): Show |
1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.589-2463_589-2462i others(26): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080668 | ||||||
chr2:219080669
|
T | A | 100 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0030others(97): Show | 100 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.589-2463A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080669 | ||||||
chr2:219080688
|
T | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2482A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080688 | ||||||
chr2:219080688
|
T | TAA | 100 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0030others(97): Show | 100 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.589-2483_589-2482i others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080688 | ||||||
chr2:219080691
|
TTA | T | 31 | a0001c0001t0002g0027a0001c0001t0002g0029a0001c0001t0002g0063others(28): Show | 31 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.589-2487_589-2486d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080691 | ||||||
chr2:219080693
|
A | ATATATAT others(39): Show |
1 | a0001c0001t0014g0085 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.589-2488_589-2487i others(48): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080693 | ||||||
chr2:219080693
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0002g0033a0001c0001t0002g0116 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.589-2488_589-2487i others(24): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080693 | ||||||
chr2:219080693
|
A | ATATATGC others(13): Show |
97 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0030others(94): Show | 97 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.589-2488_589-2487i others(22): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080693 | ||||||
chr2:219080814
|
G | T | 1 | a0001c0001t0002g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.589-2608C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080814 | ||||||
chr2:219080924
|
A | G | 12 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(9): Show | 13 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.589-2718T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080924 | ||||||
chr2:219080992
|
G | T | 3 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0010g0335 | 3 | HG02071.hp2 HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.589-2786C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080992 | ||||||
chr2:219080996
|
A | G | 110 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(107): Show | 110 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.589-2790T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219080996 | ||||||
chr2:219081084
|
C | A | 1 | a0001c0001t0002g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.589-2878G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081084 | ||||||
chr2:219081086
|
A | G | 1 | a0001c0001t0002g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.589-2880T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081086 | ||||||
chr2:219081114
|
A | G | 2 | a0001c0001t0005g0042a0001c0001t0037g0072 | 2 | HG03492.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.589-2908T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081114 | ||||||
chr2:219081133
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.589-2927A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081133 | ||||||
chr2:219081223
|
T | C | 1 | a0001c0001t0028g0250 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.589-3017A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081223 | ||||||
chr2:219081233
|
A | G | 1 | a0001c0001t0002g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.589-3027T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081233 | ||||||
chr2:219081294
|
G | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0306 | 2 | HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.589-3088C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081294 | ||||||
chr2:219081383
|
G | A | 8 | a0001c0001t0001g0240a0001c0001t0001g0283a0001c0001t0001g0306others(5): Show | 8 | HG02738.hp1 HG02897.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.589-3177C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081383 | ||||||
chr2:219081397
|
G | C | 5 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(2): Show | 6 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-3191C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081397 | ||||||
chr2:219081419
|
A | G | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.589-3213T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081419 | ||||||
chr2:219081459
|
A | C | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-3253T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081459 | ||||||
chr2:219081510
|
T | C | 3 | a0001c0001t0002g0109a0001c0001t0002g0110a0001c0001t0002g0113 | 3 | NA18957.hp2 NA19012.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.589-3304A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081510 | ||||||
chr2:219081639
|
T | C | 11 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(8): Show | 12 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.589-3433A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081639 | ||||||
chr2:219081916
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.589-3710G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081916 | ||||||
chr2:219081941
|
A | T | 2 | a0001c0001t0008g0142a0001c0001t0008g0143 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.589-3735T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219081941 | ||||||
chr2:219082011
|
G | T | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.589-3805C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082011 | ||||||
chr2:219082252
|
A | G | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.589-4046T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082252 | ||||||
chr2:219082280
|
G | A | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(68): Show | 73 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.589-4074C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082280 | ||||||
chr2:219082395
|
A | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-4189T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082395 | ||||||
chr2:219082458
|
T | G | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-4252A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082458 | ||||||
chr2:219082462
|
A | G | 110 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(107): Show | 110 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.589-4256T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082462 | ||||||
chr2:219082482
|
A | T | 1 | a0001c0001t0002g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.589-4276T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082482 | ||||||
chr2:219082587
|
A | T | 1 | a0001c0001t0002g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.589-4381T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082587 | ||||||
chr2:219082588
|
C | A | 1 | a0001c0001t0002g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.589-4382G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082588 | ||||||
chr2:219082728
|
A | T | 1 | a0001c0001t0002g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.589-4522T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082728 | ||||||
chr2:219082730
|
C | A | 12 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(9): Show | 13 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.589-4524G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082730 | ||||||
chr2:219082736
|
G | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18949.hp1 NA18966.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.589-4530C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082736 | ||||||
chr2:219082747
|
C | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-4541G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082747 | ||||||
chr2:219082963
|
G | A | 40 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(37): Show | 44 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.589-4757C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082963 | ||||||
chr2:219082969
|
A | G | 198 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(195): Show | 203 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.589-4763T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219082969 | ||||||
chr2:219083016
|
A | T | 1 | a0001c0001t0004g0070 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.589-4810T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083016 | ||||||
chr2:219083018
|
A | T | 1 | a0001c0001t0004g0070 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.589-4812T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083018 | ||||||
chr2:219083019
|
A | T | 1 | a0001c0001t0004g0070 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.589-4813T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083019 | ||||||
chr2:219083049
|
T | C | 199 | a0001c0001t0001g0315a0001c0001t0002g0023a0001c0001t0002g0026others(196): Show | 204 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.589-4843A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083049 | ||||||
chr2:219083077
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589-4871A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083077 | ||||||
chr2:219083162
|
A | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0297 | 2 | NA19004.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.589-4956T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083162 | ||||||
chr2:219083205
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.589-4999G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083205 | ||||||
chr2:219083207
|
A | T | 1 | a0001c0001t0002g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.589-5001T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083207 | ||||||
chr2:219083257
|
C | T | 5 | a0001c0001t0003g0001a0001c0001t0003g0136a0001c0001t0003g0137others(2): Show | 6 | NA18747.hp2 NA18947.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-5051G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083257 | ||||||
chr2:219083370
|
A | G | 198 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(195): Show | 203 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.589-5164T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083370 | ||||||
chr2:219083377
|
G | T | 4 | a0001c0001t0006g0098a0002c0002t0006g0146a0002c0002t0006g0147others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-5171C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083377 | ||||||
chr2:219083442
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.589-5236G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083442 | ||||||
chr2:219083471
|
G | GA | 126 | a0001c0001t0001g0315a0001c0001t0002g0023a0001c0001t0002g0026others(123): Show | 126 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.589-5266dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083471 | ||||||
chr2:219083471
|
G | GAA | 66 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 70 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.589-5267_589-5266d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083471 | ||||||
chr2:219083471
|
G | GAAA | 7 | a0001c0001t0002g0030a0001c0001t0012g0002a0001c0001t0012g0117others(4): Show | 8 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.589-5268_589-5266d others(5): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083471 | ||||||
chr2:219083709
|
C | T | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.589-5503G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083709 | ||||||
chr2:219083897
|
A | G | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-5691T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219083897 | ||||||
chr2:219084007
|
C | CT | 65 | a0001c0001t0001g0208a0001c0001t0001g0218a0001c0001t0001g0251others(62): Show | 70 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.589-5802dupA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219084007 | ||||||
chr2:219084007
|
CT | C | 15 | a0001c0001t0001g0258a0001c0001t0006g0098a0001c0001t0013g0131others(12): Show | 15 | HG01884.hp2 HG01975.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.589-5802delA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219084007 | ||||||
chr2:219084025
|
G | A | 3 | a0001c0001t0002g0038a0001c0001t0002g0089a0001c0001t0002g0288 | 3 | NA18982.hp1 NA18983.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.589-5819C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219084025 | ||||||
chr2:219084289
|
G | A | 4 | a0001c0001t0010g0161a0001c0001t0010g0333a0001c0001t0010g0334others(1): Show | 4 | HG02071.hp2 HG02083.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-6083C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219084289 | ||||||
chr2:219084462
|
C | T | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(68): Show | 73 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.589-6256G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219084462 | ||||||
chr2:219084589
|
C | T | 1 | a0001c0001t0002g0288 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.589-6383G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219084589 | ||||||
chr2:219084664
|
T | C | 3 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0094 | 3 | HG02258.hp2 HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.589-6458A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219084664 | ||||||
chr2:219084866
|
G | A | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-6660C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219084866 | ||||||
chr2:219084871
|
G | A | 110 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(107): Show | 110 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.589-6665C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219084871 | ||||||
chr2:219085011
|
C | A | 1 | a0001c0001t0001g0206 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.589-6805G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085011 | ||||||
chr2:219085084
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.589-6878A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085084 | ||||||
chr2:219085085
|
G | A | 4 | a0001c0001t0002g0031a0001c0001t0002g0035a0001c0001t0002g0037others(1): Show | 4 | HG01978.hp2 HG01981.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-6879C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085085 | ||||||
chr2:219085191
|
A | T | 91 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0030others(88): Show | 91 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.589-6985T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085191 | ||||||
chr2:219085216
|
T | C | 1 | a0001c0001t0044g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.589-7010A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085216 | ||||||
chr2:219085262
|
C | T | 12 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(9): Show | 13 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.589-7056G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085262 | ||||||
chr2:219085270
|
T | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-7064A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085270 | ||||||
chr2:219085388
|
G | C | 198 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(195): Show | 203 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.589-7182C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085388 | ||||||
chr2:219085498
|
G | A | 127 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(124): Show | 127 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.589-7292C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085498 | ||||||
chr2:219085582
|
G | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-7376C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085582 | ||||||
chr2:219085647
|
AAC | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-7443_589-7442d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085647 | ||||||
chr2:219085779
|
T | C | 12 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(9): Show | 13 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.589-7573A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085779 | ||||||
chr2:219085790
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.589-7584T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085790 | ||||||
chr2:219085938
|
G | A | 4 | a0001c0001t0002g0313a0001c0001t0016g0104a0001c0001t0016g0105others(1): Show | 4 | HG03139.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-7732C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085938 | ||||||
chr2:219085945
|
A | G | 12 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(9): Show | 13 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.589-7739T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085945 | ||||||
chr2:219085947
|
A | G | 110 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(107): Show | 110 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.589-7741T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219085947 | ||||||
chr2:219086107
|
C | G | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.589-7901G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219086107 | ||||||
chr2:219086176
|
T | C | 7 | a0001c0001t0006g0098a0002c0002t0006g0146a0002c0002t0006g0147others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-7970A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219086176 | ||||||
chr2:219086484
|
C | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-8278G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219086484 | ||||||
chr2:219087144
|
G | A | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.589-8938C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219087144 | ||||||
chr2:219087174
|
A | G | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-8968T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219087174 | ||||||
chr2:219087218
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0249a0001c0001t0001g0251others(1): Show | 4 | HG02523.hp1 NA18951.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-9012G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219087218 | ||||||
chr2:219087380
|
C | CT | 111 | a0001c0001t0001g0208a0001c0001t0002g0023a0001c0001t0002g0026others(108): Show | 111 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.589-9175dupA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219087380 | ||||||
chr2:219087524
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.589-9318T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219087524 | ||||||
chr2:219087606
|
G | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-9400C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219087606 | ||||||
chr2:219087622
|
T | C | 1 | a0001c0001t0008g0145 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.589-9416A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219087622 | ||||||
chr2:219087705
|
T | G | 1 | a0001c0001t0002g0095 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.589-9499A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219087705 | ||||||
chr2:219088020
|
C | T | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-9814G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088020 | ||||||
chr2:219088300
|
A | G | 1 | a0001c0001t0002g0096 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.589-10094T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088300 | ||||||
chr2:219088304
|
A | G | 2 | a0001c0001t0007g0316a0001c0001t0007g0317 | 2 | NA18964.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.589-10098T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088304 | ||||||
chr2:219088361
|
C | A | 1 | a0001c0001t0003g0172 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.589-10155G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088361 | ||||||
chr2:219088396
|
G | A | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-10190C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088396 | ||||||
chr2:219088479
|
T | C | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-10273A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088479 | ||||||
chr2:219088620
|
T | C | 9 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(6): Show | 9 | HG00673.hp1 NA18949.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-10414A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088620 | ||||||
chr2:219088713
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589-10507C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088713 | ||||||
chr2:219088812
|
T | G | 1 | a0002c0002t0006g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.589-10606A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088812 | ||||||
chr2:219088867
|
C | T | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(68): Show | 73 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.589-10661G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088867 | ||||||
chr2:219088868
|
G | A | 1 | a0001c0001t0002g0101 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.589-10662C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088868 | ||||||
chr2:219088873
|
C | T | 1 | a0001c0001t0003g0136 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.589-10667G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088873 | ||||||
chr2:219088874
|
G | A | 122 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(119): Show | 124 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.589-10668C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088874 | ||||||
chr2:219088913
|
T | G | 15 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(12): Show | 16 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-10707A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088913 | ||||||
chr2:219088917
|
A | G | 1 | a0001c0001t0008g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.589-10711T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219088917 | ||||||
chr2:219089010
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.589-10804C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089010 | ||||||
chr2:219089090
|
A | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0305a0001c0001t0001g0337 | 3 | HG02015.hp1 HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.589-10884T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089090 | ||||||
chr2:219089110
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.589-10904G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089110 | ||||||
chr2:219089174
|
G | A | 1 | a0001c0001t0046g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.589-10968C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089174 | ||||||
chr2:219089231
|
C | T | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0280 | 3 | HG03098.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.589-11025G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089231 | ||||||
chr2:219089253
|
C | T | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-11047G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089253 | ||||||
chr2:219089485
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.589-11279C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089485 | ||||||
chr2:219089565
|
C | G | 4 | a0001c0001t0011g0069a0001c0001t0011g0330a0001c0001t0011g0331others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-11359G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089565 | ||||||
chr2:219089616
|
A | G | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.589-11410T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089616 | ||||||
chr2:219089620
|
A | C | 15 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(12): Show | 16 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-11414T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089620 | ||||||
chr2:219089801
|
C | T | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-11595G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089801 | ||||||
chr2:219089875
|
G | A | 1 | a0001c0001t0006g0098 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.589-11669C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219089875 | ||||||
chr2:219090183
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.589-11977A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090183 | ||||||
chr2:219090251
|
G | T | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-12045C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090251 | ||||||
chr2:219090355
|
A | T | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.589-12149T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090355 | ||||||
chr2:219090371
|
G | A | 127 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(124): Show | 127 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.589-12165C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090371 | ||||||
chr2:219090384
|
C | A | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-12178G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090384 | ||||||
chr2:219090587
|
C | T | 15 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(12): Show | 16 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-12381G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090587 | ||||||
chr2:219090649
|
T | C | 15 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(12): Show | 16 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-12443A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090649 | ||||||
chr2:219090655
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.589-12449T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090655 | ||||||
chr2:219090711
|
C | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-12505G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090711 | ||||||
chr2:219090712
|
C | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0275 | 2 | NA18979.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.589-12506G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090712 | ||||||
chr2:219090713
|
G | A | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-12507C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219090713 | ||||||
chr2:219091198
|
C | T | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.589-12992G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219091198 | ||||||
chr2:219091214
|
C | G | 53 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(50): Show | 57 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.589-13008G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219091214 | ||||||
chr2:219091290
|
G | A | 127 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(124): Show | 127 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.589-13084C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219091290 | ||||||
chr2:219091414
|
G | A | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-13208C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219091414 | ||||||
chr2:219091507
|
T | C | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-13301A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219091507 | ||||||
chr2:219091657
|
T | C | 2 | a0001c0001t0020g0223a0001c0001t0020g0224 | 2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.589-13451A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219091657 | ||||||
chr2:219091804
|
ATGTGTAT others(12): Show |
A | 197 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(194): Show | 202 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.589-13617_589-1359 others(23): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219091804 | ||||||
chr2:219091962
|
T | G | 15 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(12): Show | 16 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-13756A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219091962 | ||||||
chr2:219092228
|
A | C | 1 | a0001c0001t0034g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.589-14022T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219092228 | ||||||
chr2:219092293
|
C | CA | 8 | a0001c0001t0001g0308a0001c0001t0002g0064a0001c0001t0003g0338others(5): Show | 8 | HG01993.hp1 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.589-14088dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219092293 | ||||||
chr2:219092293
|
C | CAA | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-14089_589-1408 others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219092293 | ||||||
chr2:219092293
|
C | CAAA | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-14090_589-1408 others(7): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219092293 | ||||||
chr2:219092521
|
T | C | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-14315A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219092521 | ||||||
chr2:219092540
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.589-14334G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219092540 | ||||||
chr2:219092967
|
G | A | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-14761C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219092967 | ||||||
chr2:219092968
|
C | T | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-14762G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219092968 | ||||||
chr2:219093141
|
T | C | 5 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(2): Show | 6 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-14935A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093141 | ||||||
chr2:219093290
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | NA18974.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.589-15084C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093290 | ||||||
chr2:219093308
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0010g0161 | 2 | NA18942.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.589-15102C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093308 | ||||||
chr2:219093458
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.589-15252G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093458 | ||||||
chr2:219093494
|
G | A | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-15288C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093494 | ||||||
chr2:219093635
|
C | G | 1 | a0001c0001t0001g0282 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.589-15429G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093635 | ||||||
chr2:219093678
|
C | G | 11 | a0001c0001t0002g0027a0001c0001t0002g0029a0001c0001t0002g0073others(8): Show | 11 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.589-15472G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093678 | ||||||
chr2:219093683
|
T | C | 1 | a0001c0001t0002g0121 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.589-15477A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093683 | ||||||
chr2:219093740
|
C | T | 247 | a0001c0001t0001g0084a0001c0001t0001g0162a0001c0001t0001g0182others(244): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.589-15534G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093740 | ||||||
chr2:219093756
|
A | T | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-15550T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093756 | ||||||
chr2:219093798
|
G | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-15592C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093798 | ||||||
chr2:219093806
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.589-15600C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219093806 | ||||||
chr2:219094181
|
C | T | 53 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(50): Show | 57 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.589-15975G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219094181 | ||||||
chr2:219094344
|
G | A | 3 | a0001c0001t0002g0026a0001c0001t0002g0119a0001c0001t0002g0120 | 3 | HG01175.hp1 HG01891.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.589-16138C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219094344 | ||||||
chr2:219094445
|
G | C | 3 | a0001c0001t0001g0266a0001c0001t0001g0271a0001c0001t0001g0274 | 3 | HG00609.hp2 NA18956.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.589-16239C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219094445 | ||||||
chr2:219094657
|
G | C | 4 | a0001c0001t0011g0069a0001c0001t0011g0330a0001c0001t0011g0331others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-16451C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219094657 | ||||||
chr2:219094705
|
C | T | 2 | a0002c0002t0006g0148a0002c0002t0006g0149 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.589-16499G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219094705 | ||||||
chr2:219094736
|
C | T | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.589-16530G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219094736 | ||||||
chr2:219094823
|
A | G | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.589-16617T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219094823 | ||||||
chr2:219094869
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.589-16663G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219094869 | ||||||
chr2:219095147
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.589-16941C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219095147 | ||||||
chr2:219095357
|
T | A | 13 | a0001c0001t0006g0098a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.589-17151A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219095357 | ||||||
chr2:219095664
|
T | C | 1 | a0001c0001t0011g0331 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.589-17458A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219095664 | ||||||
chr2:219095821
|
C | A | 49 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(46): Show | 53 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.589-17615G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219095821 | ||||||
chr2:219095830
|
A | G | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.589-17624T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219095830 | ||||||
chr2:219095921
|
G | A | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-17715C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219095921 | ||||||
chr2:219096016
|
A | G | 12 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173others(9): Show | 12 | NA18966.hp2 NA18968.hp2 NA18970.hp2 others(9): Show |
intron_variant | MODIFIER | c.589-17810T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096016 | ||||||
chr2:219096219
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.589-18013C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096219 | ||||||
chr2:219096295
|
T | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-18089A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096295 | ||||||
chr2:219096305
|
T | A | 1 | a0001c0001t0003g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.589-18099A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096305 | ||||||
chr2:219096351
|
G | A | 4 | a0001c0001t0011g0069a0001c0001t0011g0330a0001c0001t0011g0331others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-18145C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096351 | ||||||
chr2:219096354
|
A | G | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-18148T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096354 | ||||||
chr2:219096387
|
C | G | 15 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(12): Show | 16 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-18181G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096387 | ||||||
chr2:219096494
|
T | TAAGCTAT others(2): Show |
9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-18289_589-1828 others(13): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096494 | ||||||
chr2:219096569
|
G | A | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-18363C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096569 | ||||||
chr2:219096862
|
T | C | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-18656A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096862 | ||||||
chr2:219096938
|
G | C | 196 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(193): Show | 201 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.589-18732C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219096938 | ||||||
chr2:219097220
|
C | T | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-19014G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219097220 | ||||||
chr2:219097569
|
C | T | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-19363G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219097569 | ||||||
chr2:219097903
|
C | T | 4 | a0001c0001t0001g0162a0001c0001t0001g0197a0001c0001t0001g0205others(1): Show | 4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-19697G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219097903 | ||||||
chr2:219097970
|
T | C | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-19764A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219097970 | ||||||
chr2:219097992
|
A | G | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.589-19786T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219097992 | ||||||
chr2:219098218
|
G | C | 1 | a0001c0001t0011g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.589-20012C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219098218 | ||||||
chr2:219098626
|
G | T | 1 | a0001c0001t0019g0243 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.589-20420C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219098626 | ||||||
chr2:219098799
|
A | T | 1 | a0001c0001t0003g0201 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.589-20593T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219098799 | ||||||
chr2:219098828
|
C | T | 90 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0030others(87): Show | 90 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.589-20622G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219098828 | ||||||
chr2:219098848
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.589-20642G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219098848 | ||||||
chr2:219098919
|
G | A | 5 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(2): Show | 5 | NA18941.hp2 NA18942.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-20713C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219098919 | ||||||
chr2:219099039
|
G | A | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.589-20833C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219099039 | ||||||
chr2:219099119
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.589-20913G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219099119 | ||||||
chr2:219099132
|
GT | G | 48 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(45): Show | 52 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.589-20927delA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219099132 | ||||||
chr2:219099588
|
T | C | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-21382A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219099588 | ||||||
chr2:219099698
|
G | GT | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-21493dupA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219099698 | ||||||
chr2:219099721
|
A | G | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-21515T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219099721 | ||||||
chr2:219099741
|
C | CGGCAGAA others(14): Show |
3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-21556_589-2153 others(25): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219099741 | ||||||
chr2:219099802
|
G | C | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-21596C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219099802 | ||||||
chr2:219099883
|
T | C | 13 | a0001c0001t0006g0098a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.589-21677A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219099883 | ||||||
chr2:219099981
|
G | A | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-21775C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219099981 | ||||||
chr2:219100447
|
C | CA | 131 | a0001c0001t0001g0133a0001c0001t0001g0252a0001c0001t0001g0253others(128): Show | 131 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.589-22242dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219100447 | ||||||
chr2:219100527
|
T | C | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-22321A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219100527 | ||||||
chr2:219100609
|
TA | T | 36 | a0001c0001t0001g0013a0001c0001t0001g0228a0001c0001t0001g0304others(33): Show | 37 | HG00558.hp2 HG01167.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.589-22404delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219100609 | ||||||
chr2:219100609
|
TAA | T | 6 | a0001c0001t0003g0012a0001c0001t0010g0161a0001c0001t0010g0333others(3): Show | 6 | HG02071.hp2 HG02083.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-22405_589-2240 others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219100609 | ||||||
chr2:219100717
|
A | C | 7 | a0001c0001t0006g0098a0002c0002t0006g0146a0002c0002t0006g0147others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-22511T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219100717 | ||||||
chr2:219100900
|
A | G | 1 | a0001c0001t0002g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.589-22694T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219100900 | ||||||
chr2:219100960
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.589-22754G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219100960 | ||||||
chr2:219101061
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.589-22855A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101061 | ||||||
chr2:219101098
|
T | C | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-22892A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101098 | ||||||
chr2:219101175
|
T | C | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-22969A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101175 | ||||||
chr2:219101261
|
C | T | 127 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(124): Show | 127 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.589-23055G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101261 | ||||||
chr2:219101407
|
G | A | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-23201C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101407 | ||||||
chr2:219101524
|
T | C | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-23318A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101524 | ||||||
chr2:219101637
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.589-23431G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101637 | ||||||
chr2:219101720
|
C | CT | 7 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0003g0138others(4): Show | 7 | HG01346.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-23515dupA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101720 | ||||||
chr2:219101757
|
C | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG00099.hp1 HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.589-23551G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101757 | ||||||
chr2:219101790
|
A | G | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.589-23584T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101790 | ||||||
chr2:219101893
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0297 | 2 | NA19004.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.589-23687A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101893 | ||||||
chr2:219101918
|
G | A | 2 | a0001c0001t0011g0069a0001c0001t0011g0332 | 2 | HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.589-23712C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101918 | ||||||
chr2:219101960
|
G | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-23754C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101960 | ||||||
chr2:219101970
|
C | T | 4 | a0001c0001t0011g0069a0001c0001t0011g0330a0001c0001t0011g0331others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-23764G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219101970 | ||||||
chr2:219102020
|
A | G | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-23814T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102020 | ||||||
chr2:219102031
|
T | C | 1 | a0002c0002t0024g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.589-23825A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102031 | ||||||
chr2:219102079
|
G | C | 52 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(49): Show | 56 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.589-23873C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102079 | ||||||
chr2:219102140
|
T | C | 194 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(191): Show | 199 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.589-23934A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102140 | ||||||
chr2:219102226
|
A | C | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-24020T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102226 | ||||||
chr2:219102465
|
T | C | 1 | a0001c0001t0003g0338 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.589-24259A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102465 | ||||||
chr2:219102526
|
C | T | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-24320G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102526 | ||||||
chr2:219102605
|
A | G | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-24399T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102605 | ||||||
chr2:219102618
|
A | C | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-24412T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102618 | ||||||
chr2:219102658
|
T | C | 328 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(325): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.589-24452A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102658 | ||||||
chr2:219102832
|
C | T | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-24626G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102832 | ||||||
chr2:219102849
|
CAAAAAAT others(170): Show |
C | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-24820_589-2464 others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219102849 | ||||||
chr2:219103004
|
C | CA | 160 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 164 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.589-24799dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103004 | ||||||
chr2:219103004
|
C | CAA | 55 | a0001c0001t0001g0214a0001c0001t0001g0329a0001c0001t0002g0029others(52): Show | 56 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.589-24800_589-2479 others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103004 | ||||||
chr2:219103004
|
C | CAAA | 7 | a0001c0001t0002g0027a0001c0001t0002g0074a0001c0001t0002g0078others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-24801_589-2479 others(7): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103004 | ||||||
chr2:219103173
|
G | GA | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0242others(4): Show | 7 | HG01099.hp1 HG03654.hp2 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-24968dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103173 | ||||||
chr2:219103173
|
GA | G | 64 | a0001c0001t0002g0168a0001c0001t0003g0003a0001c0001t0003g0004others(61): Show | 68 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.589-24968delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103173 | ||||||
chr2:219103175
|
A | G | 1 | a0001c0001t0003g0004 | 2 | HG00140.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.589-24969T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103175 | ||||||
chr2:219103194
|
CTG | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-24990_589-2498 others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103194 | ||||||
chr2:219103283
|
C | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-25077G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103283 | ||||||
chr2:219103368
|
C | T | 7 | a0001c0001t0005g0020a0001c0001t0008g0140a0001c0001t0008g0141others(4): Show | 7 | HG00639.hp2 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-25162G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103368 | ||||||
chr2:219103395
|
A | T | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG03130.hp2 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.589-25189T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103395 | ||||||
chr2:219103470
|
T | TACATACA others(5): Show |
1 | a0001c0001t0003g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.589-25265_589-2526 others(16): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103470 | ||||||
chr2:219103471
|
T | A | 1 | a0001c0001t0003g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.589-25265A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103471 | ||||||
chr2:219103474
|
C | A | 1 | a0001c0001t0003g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.589-25268G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103474 | ||||||
chr2:219103533
|
C | T | 2 | a0001c0001t0020g0223a0001c0001t0020g0224 | 2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.589-25327G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103533 | ||||||
chr2:219103555
|
C | T | 1 | a0001c0001t0003g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589-25349G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103555 | ||||||
chr2:219103572
|
G | C | 3 | a0001c0001t0002g0030a0001c0001t0002g0034a0001c0001t0002g0036 | 3 | NA18949.hp2 NA18961.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.589-25366C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103572 | ||||||
chr2:219103700
|
A | G | 55 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(52): Show | 59 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.589-25494T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103700 | ||||||
chr2:219103736
|
T | G | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.589-25530A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103736 | ||||||
chr2:219103854
|
T | C | 63 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(60): Show | 67 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.589-25648A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103854 | ||||||
chr2:219103934
|
C | A | 1 | a0001c0001t0002g0038 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.589-25728G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219103934 | ||||||
chr2:219104063
|
T | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0242a0001c0001t0001g0244 | 3 | NA18944.hp2 NA18990.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.589-25857A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104063 | ||||||
chr2:219104147
|
G | A | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(68): Show | 73 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.589-25941C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104147 | ||||||
chr2:219104165
|
C | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-25959G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104165 | ||||||
chr2:219104363
|
G | C | 51 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(48): Show | 54 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.589-26157C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104363 | ||||||
chr2:219104375
|
A | G | 53 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(50): Show | 56 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.589-26169T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104375 | ||||||
chr2:219104586
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | NA18974.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.589-26380C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104586 | ||||||
chr2:219104708
|
C | A | 6 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(3): Show | 7 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-26502G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104708 | ||||||
chr2:219104709
|
A | C | 8 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0218others(5): Show | 8 | HG01261.hp1 HG01361.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.589-26503T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104709 | ||||||
chr2:219104709
|
ACAC | A | 50 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(47): Show | 53 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.589-26506_589-2650 others(7): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104709 | ||||||
chr2:219104710
|
C | A | 1 | a0001c0001t0003g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.589-26504G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104710 | ||||||
chr2:219104714
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.589-26508G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104714 | ||||||
chr2:219104716
|
C | A | 7 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-26510G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104716 | ||||||
chr2:219104726
|
G | T | 2 | a0001c0001t0013g0341a0001c0001t0013g0342 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589-26520C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219104726 | ||||||
chr2:219105022
|
C | T | 9 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-26816G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219105022 | ||||||
chr2:219105076
|
G | A | 126 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(123): Show | 126 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.589-26870C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219105076 | ||||||
chr2:219105321
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.589-27115C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219105321 | ||||||
chr2:219105501
|
C | T | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.589-27295G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219105501 | ||||||
chr2:219105600
|
C | A | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.589-27394G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219105600 | ||||||
chr2:219105779
|
T | C | 1 | a0001c0001t0003g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.589-27573A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219105779 | ||||||
chr2:219105806
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.589-27600G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219105806 | ||||||
chr2:219105828
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.589-27622G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219105828 | ||||||
chr2:219105864
|
A | G | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.589-27658T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219105864 | ||||||
chr2:219105976
|
T | C | 1 | a0001c0001t0044g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.589-27770A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219105976 | ||||||
chr2:219106089
|
C | T | 4 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-27883G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106089 | ||||||
chr2:219106118
|
A | T | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.589-27912T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106118 | ||||||
chr2:219106189
|
T | C | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.589-27983A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106189 | ||||||
chr2:219106335
|
G | C | 8 | a0001c0001t0001g0240a0001c0001t0001g0283a0001c0001t0001g0306others(5): Show | 8 | HG02738.hp1 HG02897.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.589-28129C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106335 | ||||||
chr2:219106498
|
A | G | 1 | a0001c0001t0002g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.589-28292T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106498 | ||||||
chr2:219106706
|
T | G | 1 | a0001c0001t0044g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.589-28500A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106706 | ||||||
chr2:219106718
|
C | T | 12 | a0001c0001t0006g0098a0002c0002t0006g0124a0002c0002t0006g0125others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.589-28512G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106718 | ||||||
chr2:219106723
|
T | A | 1 | a0001c0001t0003g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.589-28517A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106723 | ||||||
chr2:219106795
|
A | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 58 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.589-28589T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106795 | ||||||
chr2:219106796
|
A | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 58 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.589-28590T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106796 | ||||||
chr2:219106804
|
A | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 58 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.589-28598T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106804 | ||||||
chr2:219106808
|
T | C | 54 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 58 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.589-28602A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219106808 | ||||||
chr2:219107062
|
T | C | 7 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-28856A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219107062 | ||||||
chr2:219107241
|
A | G | 4 | a0001c0001t0011g0069a0001c0001t0011g0330a0001c0001t0011g0331others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-29035T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219107241 | ||||||
chr2:219107278
|
G | A | 7 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-29072C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219107278 | ||||||
chr2:219107281
|
G | A | 7 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-29075C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219107281 | ||||||
chr2:219107297
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00544.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.589-29091G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219107297 | ||||||
chr2:219107301
|
T | G | 1 | a0001c0001t0010g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.589-29095A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219107301 | ||||||
chr2:219107321
|
T | A | 39 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(36): Show | 43 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.589-29115A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219107321 | ||||||
chr2:219107653
|
G | C | 196 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(193): Show | 201 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.589-29447C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219107653 | ||||||
chr2:219107688
|
G | C | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0280 | 3 | HG03098.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.589-29482C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219107688 | ||||||
chr2:219107852
|
G | A | 63 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(60): Show | 68 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.589-29646C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219107852 | ||||||
chr2:219108262
|
G | A | 63 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(60): Show | 68 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.589-30056C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219108262 | ||||||
chr2:219108275
|
G | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-30069C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219108275 | ||||||
chr2:219108312
|
G | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-30106C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219108312 | ||||||
chr2:219108419
|
C | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-30213G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219108419 | ||||||
chr2:219108513
|
TTAC | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-30310_589-3030 others(7): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219108513 | ||||||
chr2:219108917
|
T | C | 2 | a0001c0001t0021g0169a0001c0001t0021g0170 | 2 | HG02293.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.589-30711A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219108917 | ||||||
chr2:219108968
|
A | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0242a0001c0001t0001g0244 | 3 | NA18944.hp2 NA18990.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.589-30762T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219108968 | ||||||
chr2:219109023
|
G | C | 48 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(45): Show | 51 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.589-30817C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109023 | ||||||
chr2:219109093
|
C | T | 13 | a0001c0001t0006g0098a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.589-30887G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109093 | ||||||
chr2:219109116
|
A | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0306 | 2 | HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.589-30910T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109116 | ||||||
chr2:219109121
|
GAAC | G | 7 | a0001c0001t0001g0040a0001c0001t0001g0267a0001c0001t0001g0275others(4): Show | 7 | HG01123.hp2 HG01928.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-30918_589-3091 others(7): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109121 | ||||||
chr2:219109130
|
G | GC | 4 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-30925dupG | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109130 | ||||||
chr2:219109430
|
G | T | 109 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(106): Show | 109 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.589-31224C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109430 | ||||||
chr2:219109454
|
C | T | 2 | a0001c0001t0020g0223a0001c0001t0020g0224 | 2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.589-31248G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109454 | ||||||
chr2:219109460
|
C | T | 13 | a0001c0001t0006g0098a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.589-31254G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109460 | ||||||
chr2:219109622
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.589-31416G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109622 | ||||||
chr2:219109672
|
G | A | 7 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-31466C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109672 | ||||||
chr2:219109752
|
C | T | 3 | a0001c0001t0006g0098a0002c0002t0006g0146a0002c0002t0006g0150 | 3 | HG02257.hp1 HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.589-31546G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109752 | ||||||
chr2:219109967
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.589-31761A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219109967 | ||||||
chr2:219110130
|
T | C | 55 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(52): Show | 59 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.589-31924A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110130 | ||||||
chr2:219110160
|
A | G | 6 | a0001c0001t0002g0023a0001c0001t0002g0097a0001c0001t0002g0099others(3): Show | 6 | HG00099.hp2 HG01123.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-31954T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110160 | ||||||
chr2:219110173
|
T | C | 1 | a0001c0001t0021g0170 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.589-31967A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110173 | ||||||
chr2:219110200
|
C | T | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.589-31994G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110200 | ||||||
chr2:219110237
|
A | C | 1 | a0001c0001t0001g0182 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.589-32031T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110237 | ||||||
chr2:219110326
|
T | C | 65 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(62): Show | 69 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.589-32120A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110326 | ||||||
chr2:219110359
|
T | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-32153A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110359 | ||||||
chr2:219110458
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.589-32252C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110458 | ||||||
chr2:219110684
|
C | T | 13 | a0001c0001t0006g0098a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.589-32478G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110684 | ||||||
chr2:219110705
|
AGT | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-32501_589-3250 others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110705 | ||||||
chr2:219110836
|
T | A | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.589-32630A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110836 | ||||||
chr2:219110849
|
C | G | 9 | a0001c0001t0001g0209a0001c0001t0001g0245a0001c0001t0001g0266others(6): Show | 9 | HG00609.hp2 HG02135.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.589-32643G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219110849 | ||||||
chr2:219111119
|
T | C | 1 | a0001c0001t0003g0005 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.589-32913A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111119 | ||||||
chr2:219111299
|
C | T | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.589-33093G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111299 | ||||||
chr2:219111628
|
G | GAC | 54 | a0001c0001t0001g0084a0001c0001t0001g0132a0001c0001t0001g0133others(51): Show | 55 | HG00544.hp1 HG00673.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.589-33424_589-3342 others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111628 | ||||||
chr2:219111628
|
G | GACAC | 15 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0315others(12): Show | 15 | HG00733.hp2 HG01074.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.589-33426_589-3342 others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111628 | ||||||
chr2:219111628
|
G | GACACAC | 91 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0029others(88): Show | 91 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.589-33428_589-3342 others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111628 | ||||||
chr2:219111628
|
G | GACACACA others(1): Show |
17 | a0001c0001t0002g0023a0001c0001t0002g0064a0001c0001t0003g0003others(14): Show | 18 | HG01928.hp1 HG01978.hp1 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.589-33430_589-3342 others(12): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111628 | ||||||
chr2:219111628
|
G | GACACACA others(3): Show |
17 | a0001c0001t0001g0329a0001c0001t0002g0033a0001c0001t0002g0080others(14): Show | 17 | HG01261.hp1 HG01361.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.589-33432_589-3342 others(14): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111628 | ||||||
chr2:219111628
|
G | GACACACA others(5): Show |
17 | a0001c0001t0002g0321a0001c0001t0003g0004a0001c0001t0003g0163others(14): Show | 18 | HG00140.hp2 HG01993.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.589-33434_589-3342 others(16): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111628 | ||||||
chr2:219111628
|
G | GACACACA others(7): Show |
23 | a0001c0001t0003g0001a0001c0001t0003g0136a0001c0001t0003g0137others(20): Show | 24 | HG00558.hp2 HG02135.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.589-33436_589-3342 others(18): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111628 | ||||||
chr2:219111628
|
G | GACACACA others(9): Show |
6 | a0001c0001t0003g0193a0001c0001t0003g0201a0001c0001t0003g0278others(3): Show | 6 | HG00408.hp1 HG00544.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-33438_589-3342 others(20): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111628 | ||||||
chr2:219111628
|
GAC | G | 3 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG00099.hp1 HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.589-33424_589-3342 others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111628 | ||||||
chr2:219111652
|
CACACACA others(5): Show |
C | 1 | a0001c0001t0002g0096 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.589-33458_589-3344 others(16): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111652 | ||||||
chr2:219111660
|
CACAG | C | 4 | a0001c0001t0010g0161a0001c0001t0010g0333a0001c0001t0010g0334others(1): Show | 4 | HG02071.hp2 HG02083.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-33458_589-3345 others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111660 | ||||||
chr2:219111662
|
C | G | 1 | a0001c0001t0001g0311 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.589-33456G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111662 | ||||||
chr2:219111662
|
CAG | C | 5 | a0001c0001t0012g0002a0001c0001t0012g0117a0001c0001t0012g0160others(2): Show | 6 | HG02109.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-33458_589-3345 others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111662 | ||||||
chr2:219111664
|
G | C | 189 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0312others(186): Show | 192 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.589-33458C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111664 | ||||||
chr2:219111666
|
G | C | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.589-33460C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219111666 | ||||||
chr2:219112081
|
G | A | 1 | a0001c0001t0009g0327 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.589-33875C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219112081 | ||||||
chr2:219112311
|
A | C | 196 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(193): Show | 200 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.589-34105T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219112311 | ||||||
chr2:219112398
|
C | G | 1 | a0001c0001t0003g0157 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.589-34192G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219112398 | ||||||
chr2:219112401
|
A | G | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02027.hp2 NA18950.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.589-34195T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219112401 | ||||||
chr2:219112529
|
T | C | 1 | a0001c0001t0034g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.588+34151A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219112529 | ||||||
chr2:219112791
|
C | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18949.hp1 NA18966.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.588+33889G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219112791 | ||||||
chr2:219112805
|
C | T | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588+33875G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219112805 | ||||||
chr2:219113026
|
T | C | 1 | a0001c0001t0044g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.588+33654A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113026 | ||||||
chr2:219113082
|
C | T | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG03130.hp2 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588+33598G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113082 | ||||||
chr2:219113202
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.588+33478G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113202 | ||||||
chr2:219113295
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.588+33385C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113295 | ||||||
chr2:219113499
|
A | G | 1 | a0001c0001t0003g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.588+33181T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113499 | ||||||
chr2:219113557
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.588+33123G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113557 | ||||||
chr2:219113742
|
C | A | 4 | a0001c0001t0003g0001a0001c0001t0003g0136a0001c0001t0003g0137others(1): Show | 5 | NA18747.hp2 NA18947.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+32938G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113742 | ||||||
chr2:219113864
|
C | CA | 61 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(58): Show | 65 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.588+32815dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113864 | ||||||
chr2:219113916
|
T | C | 198 | a0001c0001t0001g0315a0001c0001t0002g0023a0001c0001t0002g0026others(195): Show | 203 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.588+32764A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113916 | ||||||
chr2:219113965
|
T | G | 1 | a0001c0001t0001g0312 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.588+32715A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113965 | ||||||
chr2:219113990
|
T | C | 1 | a0001c0001t0014g0085 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.588+32690A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219113990 | ||||||
chr2:219114041
|
C | T | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.588+32639G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219114041 | ||||||
chr2:219114541
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.588+32139A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219114541 | ||||||
chr2:219114619
|
C | T | 110 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(107): Show | 110 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.588+32061G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219114619 | ||||||
chr2:219115153
|
A | AAAG | 4 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0338others(1): Show | 6 | HG00140.hp2 HG01928.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+31524_588+3152 others(7): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115153 | ||||||
chr2:219115153
|
A | AAAGAAG | 99 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(96): Show | 99 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.588+31521_588+3152 others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115153 | ||||||
chr2:219115153
|
A | AAAGAAGA others(2): Show |
8 | a0001c0001t0002g0043a0001c0001t0002g0110a0001c0001t0002g0120others(5): Show | 8 | HG00609.hp1 HG01099.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.588+31518_588+3152 others(13): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115153 | ||||||
chr2:219115153
|
A | AAAGAAGA others(5): Show |
4 | a0001c0001t0002g0063a0001c0001t0004g0022a0001c0001t0005g0024others(1): Show | 4 | HG00733.hp2 HG01106.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+31515_588+3152 others(16): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115153 | ||||||
chr2:219115153
|
A | AAAGAAGA others(8): Show |
1 | a0001c0001t0005g0165 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.588+31512_588+3152 others(19): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115153 | ||||||
chr2:219115153
|
AAAG | A | 175 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(172): Show | 178 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.588+31524_588+3152 others(7): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115153 | ||||||
chr2:219115306
|
G | A | 4 | a0001c0001t0011g0069a0001c0001t0011g0330a0001c0001t0011g0331others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+31374C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115306 | ||||||
chr2:219115446
|
G | C | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02027.hp2 NA18950.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.588+31234C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115446 | ||||||
chr2:219115494
|
A | C | 1 | a0001c0001t0001g0329 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.588+31186T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115494 | ||||||
chr2:219115707
|
T | C | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.588+30973A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115707 | ||||||
chr2:219115751
|
C | T | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.588+30929G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115751 | ||||||
chr2:219115759
|
A | T | 196 | a0001c0001t0001g0315a0001c0001t0002g0023a0001c0001t0002g0026others(193): Show | 201 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.588+30921T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115759 | ||||||
chr2:219115876
|
C | T | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.588+30804G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115876 | ||||||
chr2:219115949
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.588+30731C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219115949 | ||||||
chr2:219116015
|
AGG | A | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 64 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.588+30663_588+3066 others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219116015 | ||||||
chr2:219116019
|
C | T | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 64 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.588+30661G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219116019 | ||||||
chr2:219116231
|
A | C | 184 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(181): Show | 189 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.588+30449T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219116231 | ||||||
chr2:219116248
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.588+30432A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219116248 | ||||||
chr2:219116353
|
T | C | 117 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(114): Show | 117 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.588+30327A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219116353 | ||||||
chr2:219116355
|
A | G | 117 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(114): Show | 117 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.588+30325T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219116355 | ||||||
chr2:219116546
|
T | C | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.588+30134A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219116546 | ||||||
chr2:219116787
|
C | T | 6 | a0002c0002t0006g0124a0002c0002t0006g0125a0002c0002t0006g0126others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+29893G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219116787 | ||||||
chr2:219117100
|
G | T | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29580C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117100 | ||||||
chr2:219117162
|
A | C | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29518T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117162 | ||||||
chr2:219117163
|
A | C | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29517T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117163 | ||||||
chr2:219117168
|
G | GCAACTTT others(14): Show |
1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29511_588+2951 others(25): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117168 | ||||||
chr2:219117169
|
T | C | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29511A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117169 | ||||||
chr2:219117173
|
T | A | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29507A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117173 | ||||||
chr2:219117181
|
G | C | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29499C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117181 | ||||||
chr2:219117198
|
C | A | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29482G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117198 | ||||||
chr2:219117199
|
C | G | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29481G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117199 | ||||||
chr2:219117207
|
T | A | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29473A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117207 | ||||||
chr2:219117208
|
G | T | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29472C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117208 | ||||||
chr2:219117209
|
C | G | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29471G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117209 | ||||||
chr2:219117212
|
C | T | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29468G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117212 | ||||||
chr2:219117215
|
T | A | 1 | a0001c0001t0021g0169 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.588+29465A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117215 | ||||||
chr2:219117268
|
A | G | 1 | a0001c0001t0044g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.588+29412T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117268 | ||||||
chr2:219117378
|
C | T | 47 | a0001c0001t0001g0084a0001c0001t0001g0162a0001c0001t0001g0182others(44): Show | 47 | HG00099.hp1 HG00642.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.588+29302G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117378 | ||||||
chr2:219117514
|
C | T | 1 | a0002c0002t0006g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.588+29166G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117514 | ||||||
chr2:219117535
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.588+29145C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117535 | ||||||
chr2:219117847
|
C | T | 1 | a0001c0001t0037g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.588+28833G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117847 | ||||||
chr2:219117942
|
G | T | 53 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(50): Show | 57 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.588+28738C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117942 | ||||||
chr2:219117970
|
C | T | 110 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(107): Show | 110 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.588+28710G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219117970 | ||||||
chr2:219118007
|
C | T | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.588+28673G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118007 | ||||||
chr2:219118027
|
C | G | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.588+28653G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118027 | ||||||
chr2:219118308
|
C | T | 248 | a0001c0001t0001g0084a0001c0001t0001g0132a0001c0001t0001g0133others(245): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.588+28372G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118308 | ||||||
chr2:219118362
|
G | C | 2 | a0001c0001t0002g0033a0001c0001t0002g0116 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.588+28318C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118362 | ||||||
chr2:219118396
|
T | TG | 198 | a0001c0001t0001g0226a0001c0001t0001g0315a0001c0001t0002g0023others(195): Show | 202 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.588+28283dupC | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118396 | ||||||
chr2:219118459
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.588+28221C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118459 | ||||||
chr2:219118536
|
T | C | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.588+28144A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118536 | ||||||
chr2:219118683
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.588+27997G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118683 | ||||||
chr2:219118751
|
G | GA | 3 | a0002c0002t0006g0124a0002c0002t0006g0125a0002c0002t0006g0126 | 3 | HG02486.hp2 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.588+27928dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118751 | ||||||
chr2:219118905
|
G | A | 1 | a0001c0001t0002g0051 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.588+27775C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118905 | ||||||
chr2:219118938
|
C | T | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.588+27742G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118938 | ||||||
chr2:219118983
|
G | A | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.588+27697C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219118983 | ||||||
chr2:219119098
|
C | T | 4 | a0001c0001t0003g0001a0001c0001t0003g0136a0001c0001t0003g0137others(1): Show | 5 | NA18747.hp2 NA18947.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+27582G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219119098 | ||||||
chr2:219119152
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.588+27528C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219119152 | ||||||
chr2:219119206
|
G | A | 7 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+27474C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219119206 | ||||||
chr2:219119430
|
C | T | 5 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(2): Show | 5 | NA18941.hp2 NA18942.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+27250G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219119430 | ||||||
chr2:219119785
|
C | T | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.588+26895G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219119785 | ||||||
chr2:219119888
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588+26792C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219119888 | ||||||
chr2:219119932
|
C | G | 1 | a0001c0001t0001g0276 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.588+26748G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219119932 | ||||||
chr2:219120165
|
T | C | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.588+26515A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219120165 | ||||||
chr2:219120176
|
C | T | 190 | a0001c0001t0001g0315a0001c0001t0002g0023a0001c0001t0002g0026others(187): Show | 194 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.588+26504G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219120176 | ||||||
chr2:219120271
|
GGTGA | G | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+26405_588+2640 others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219120271 | ||||||
chr2:219120293
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.588+26387G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219120293 | ||||||
chr2:219120635
|
A | C | 109 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(106): Show | 109 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.588+26045T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219120635 | ||||||
chr2:219120724
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.588+25956G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219120724 | ||||||
chr2:219121097
|
G | T | 1 | a0001c0001t0002g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.588+25583C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121097 | ||||||
chr2:219121217
|
A | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.588+25463T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121217 | ||||||
chr2:219121281
|
C | A | 1 | a0001c0001t0007g0039 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.588+25399G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121281 | ||||||
chr2:219121464
|
T | A | 1 | a0001c0001t0001g0291 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.588+25216A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121464 | ||||||
chr2:219121465
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.588+25215G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121465 | ||||||
chr2:219121466
|
C | A | 1 | a0001c0001t0002g0067 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.588+25214G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121466 | ||||||
chr2:219121521
|
C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0043a0001c0001t0002g0064others(3): Show | 6 | HG01099.hp1 HG03239.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+25159G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121521 | ||||||
chr2:219121531
|
T | C | 50 | a0001c0001t0001g0315a0001c0001t0003g0001a0001c0001t0003g0003others(47): Show | 53 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.588+25149A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121531 | ||||||
chr2:219121570
|
G | C | 1 | a0001c0001t0010g0334 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.588+25110C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121570 | ||||||
chr2:219121627
|
G | A | 1 | a0001c0001t0003g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.588+25053C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121627 | ||||||
chr2:219121816
|
T | C | 7 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0218others(4): Show | 7 | HG01261.hp1 HG01361.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+24864A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121816 | ||||||
chr2:219121984
|
A | G | 10 | a0001c0001t0001g0209a0001c0001t0001g0245a0001c0001t0001g0266others(7): Show | 10 | HG00609.hp2 HG02135.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.588+24696T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219121984 | ||||||
chr2:219122222
|
T | C | 109 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(106): Show | 109 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.588+24458A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122222 | ||||||
chr2:219122377
|
T | G | 123 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0027others(120): Show | 123 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.588+24303A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122377 | ||||||
chr2:219122436
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.588+24244C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122436 | ||||||
chr2:219122495
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0273 | 2 | NA18944.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.588+24185T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122495 | ||||||
chr2:219122563
|
C | G | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.588+24117G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122563 | ||||||
chr2:219122652
|
T | G | 1 | a0001c0001t0002g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.588+24028A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122652 | ||||||
chr2:219122663
|
T | C | 4 | a0001c0001t0006g0098a0002c0002t0006g0146a0002c0002t0006g0147others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+24017A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122663 | ||||||
chr2:219122708
|
C | CT | 3 | a0001c0001t0001g0084a0001c0001t0001g0242a0001c0001t0001g0244 | 3 | NA18944.hp2 NA18990.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.588+23971dupA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122708 | ||||||
chr2:219122820
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0306 | 2 | HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.588+23860G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122820 | ||||||
chr2:219122857
|
C | G | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.588+23823G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122857 | ||||||
chr2:219122969
|
C | T | 13 | a0001c0001t0006g0098a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.588+23711G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219122969 | ||||||
chr2:219123000
|
G | A | 3 | a0001c0001t0002g0081a0001c0001t0007g0062a0001c0001t0007g0122 | 3 | HG02132.hp2 NA18955.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.588+23680C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123000 | ||||||
chr2:219123119
|
C | G | 8 | a0001c0001t0001g0240a0001c0001t0001g0283a0001c0001t0001g0306others(5): Show | 8 | HG02738.hp1 HG02897.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.588+23561G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123119 | ||||||
chr2:219123120
|
T | G | 8 | a0001c0001t0001g0240a0001c0001t0001g0283a0001c0001t0001g0306others(5): Show | 8 | HG02738.hp1 HG02897.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.588+23560A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123120 | ||||||
chr2:219123189
|
A | G | 5 | a0001c0001t0009g0326a0001c0001t0009g0327a0003c0003t0009g0322others(2): Show | 5 | HG01175.hp2 HG01975.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+23491T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123189 | ||||||
chr2:219123228
|
G | C | 8 | a0001c0001t0001g0240a0001c0001t0001g0283a0001c0001t0001g0306others(5): Show | 8 | HG02738.hp1 HG02897.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.588+23452C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123228 | ||||||
chr2:219123280
|
T | C | 1 | a0001c0001t0011g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.588+23400A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123280 | ||||||
chr2:219123489
|
A | G | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.588+23191T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123489 | ||||||
chr2:219123497
|
G | A | 1 | a0002c0002t0006g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.588+23183C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123497 | ||||||
chr2:219123527
|
C | T | 1 | a0001c0001t0003g0192 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.588+23153G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123527 | ||||||
chr2:219123602
|
A | T | 2 | a0001c0001t0002g0101a0001c0001t0002g0115 | 2 | HG00408.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.588+23078T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123602 | ||||||
chr2:219123798
|
G | A | 4 | a0001c0001t0011g0069a0001c0001t0011g0330a0001c0001t0011g0331others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+22882C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123798 | ||||||
chr2:219123904
|
G | A | 1 | a0001c0001t0010g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588+22776C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219123904 | ||||||
chr2:219124094
|
G | A | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.588+22586C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219124094 | ||||||
chr2:219124096
|
GA | G | 2 | a0001c0001t0003g0001a0001c0001t0003g0138 | 3 | NA18947.hp1 NA19005.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.588+22583delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219124096 | ||||||
chr2:219124163
|
G | A | 1 | a0001c0001t0003g0176 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.588+22517C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219124163 | ||||||
chr2:219124955
|
T | A | 1 | a0001c0001t0002g0110 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.588+21725A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219124955 | ||||||
chr2:219125123
|
T | TA | 191 | a0001c0001t0001g0040a0001c0001t0001g0132a0001c0001t0001g0133others(188): Show | 196 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.588+21556dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219125123 | ||||||
chr2:219125148
|
C | A | 3 | a0001c0001t0002g0030a0001c0001t0002g0034a0001c0001t0002g0036 | 3 | NA18949.hp2 NA18961.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.588+21532G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219125148 | ||||||
chr2:219125439
|
C | T | 1 | a0001c0001t0004g0075 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.588+21241G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219125439 | ||||||
chr2:219125448
|
G | A | 4 | a0001c0001t0010g0161a0001c0001t0012g0002a0001c0001t0012g0160others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+21232C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219125448 | ||||||
chr2:219125868
|
G | A | 3 | a0001c0001t0002g0168a0001c0001t0021g0169a0001c0001t0021g0170 | 3 | HG01978.hp2 HG02293.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.588+20812C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219125868 | ||||||
chr2:219125960
|
C | A | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.588+20720G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219125960 | ||||||
chr2:219126275
|
C | A | 60 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0182others(57): Show | 64 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.588+20405G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219126275 | ||||||
chr2:219126435
|
A | T | 47 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(44): Show | 50 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.588+20245T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219126435 | ||||||
chr2:219126586
|
C | T | 328 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(325): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.588+20094G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219126586 | ||||||
chr2:219126696
|
G | GTGT | 8 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0008g0140others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+19981_588+1998 others(7): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219126696 | ||||||
chr2:219126901
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.588+19779G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219126901 | ||||||
chr2:219127334
|
T | C | 47 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(44): Show | 50 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.588+19346A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219127334 | ||||||
chr2:219127440
|
C | T | 1 | a0002c0002t0024g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.588+19240G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219127440 | ||||||
chr2:219127890
|
AACC | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+18787_588+1878 others(7): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219127890 | ||||||
chr2:219128157
|
T | C | 3 | a0001c0001t0011g0330a0001c0001t0011g0331a0001c0001t0011g0332 | 3 | HG02109.hp2 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.588+18523A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219128157 | ||||||
chr2:219128472
|
G | C | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.588+18208C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219128472 | ||||||
chr2:219129014
|
T | C | 115 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(112): Show | 115 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.588+17666A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219129014 | ||||||
chr2:219129131
|
G | A | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.588+17549C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219129131 | ||||||
chr2:219129221
|
C | G | 42 | a0001c0001t0001g0162a0001c0001t0001g0197a0001c0001t0001g0202others(39): Show | 42 | HG00099.hp1 HG00642.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.588+17459G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219129221 | ||||||
chr2:219129296
|
T | C | 115 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(112): Show | 115 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.588+17384A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219129296 | ||||||
chr2:219129312
|
T | C | 1 | a0002c0002t0006g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.588+17368A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219129312 | ||||||
chr2:219129441
|
G | C | 2 | a0001c0001t0002g0096a0001c0001t0002g0118 | 2 | NA18951.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.588+17239C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219129441 | ||||||
chr2:219129523
|
G | A | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.588+17157C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219129523 | ||||||
chr2:219129545
|
G | A | 49 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(46): Show | 53 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.588+17135C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219129545 | ||||||
chr2:219129976
|
G | GT | 142 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0182others(139): Show | 142 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.588+16703dupA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219129976 | ||||||
chr2:219130044
|
CT | C | 112 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0235others(109): Show | 112 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.588+16635delA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130044 | ||||||
chr2:219130152
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.588+16528G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130152 | ||||||
chr2:219130315
|
C | T | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.588+16365G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130315 | ||||||
chr2:219130425
|
C | T | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.588+16255G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130425 | ||||||
chr2:219130464
|
G | T | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.588+16216C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130464 | ||||||
chr2:219130505
|
TA | T | 321 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(318): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.588+16174delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130505 | ||||||
chr2:219130593
|
T | C | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02027.hp2 NA18950.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.588+16087A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130593 | ||||||
chr2:219130667
|
G | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+16013C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130667 | ||||||
chr2:219130746
|
A | C | 1 | a0001c0001t0001g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.588+15934T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130746 | ||||||
chr2:219130747
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.588+15933G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130747 | ||||||
chr2:219130763
|
C | T | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.588+15917G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130763 | ||||||
chr2:219130896
|
C | T | 1 | a0001c0001t0002g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.588+15784G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219130896 | ||||||
chr2:219131067
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588+15613C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219131067 | ||||||
chr2:219131079
|
G | A | 1 | a0001c0001t0018g0220 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.588+15601C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219131079 | ||||||
chr2:219131171
|
A | G | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.588+15509T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219131171 | ||||||
chr2:219131209
|
G | C | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588+15471C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219131209 | ||||||
chr2:219131262
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.588+15418G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219131262 | ||||||
chr2:219131512
|
C | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.588+15168G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219131512 | ||||||
chr2:219131688
|
A | G | 3 | a0001c0001t0002g0030a0001c0001t0002g0034a0001c0001t0002g0036 | 3 | NA18949.hp2 NA18961.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.588+14992T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219131688 | ||||||
chr2:219131851
|
T | C | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.588+14829A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219131851 | ||||||
chr2:219131894
|
G | C | 115 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(112): Show | 115 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.588+14786C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219131894 | ||||||
chr2:219132090
|
T | C | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.588+14590A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219132090 | ||||||
chr2:219132157
|
C | A | 200 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0132others(197): Show | 204 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.588+14523G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219132157 | ||||||
chr2:219132340
|
T | C | 2 | a0001c0001t0002g0046a0001c0001t0002g0049 | 2 | NA18962.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.588+14340A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219132340 | ||||||
chr2:219132367
|
G | A | 1 | a0001c0001t0003g0158 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.588+14313C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219132367 | ||||||
chr2:219132412
|
C | T | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.588+14268G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219132412 | ||||||
chr2:219132646
|
T | C | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.588+14034A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219132646 | ||||||
chr2:219132701
|
A | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(72): Show | 77 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.588+13979T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219132701 | ||||||
chr2:219132855
|
T | A | 1 | a0001c0001t0005g0165 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.588+13825A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219132855 | ||||||
chr2:219132984
|
G | A | 1 | a0001c0001t0031g0310 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.588+13696C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219132984 | ||||||
chr2:219133156
|
C | A | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.588+13524G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219133156 | ||||||
chr2:219133170
|
T | C | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588+13510A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219133170 | ||||||
chr2:219133403
|
A | C | 115 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(112): Show | 115 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.588+13277T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219133403 | ||||||
chr2:219133405
|
A | G | 2 | a0001c0001t0002g0080a0001c0001t0002g0087 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.588+13275T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219133405 | ||||||
chr2:219133927
|
A | C | 1 | a0001c0001t0034g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.588+12753T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219133927 | ||||||
chr2:219133995
|
C | T | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+12685G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219133995 | ||||||
chr2:219134236
|
C | T | 1 | a0003c0003t0009g0323 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.588+12444G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219134236 | ||||||
chr2:219134291
|
C | G | 2 | a0001c0001t0018g0219a0001c0001t0018g0220 | 2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.588+12389G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219134291 | ||||||
chr2:219134389
|
T | A | 1 | a0001c0001t0003g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.588+12291A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219134389 | ||||||
chr2:219134500
|
T | C | 2 | a0003c0003t0009g0322a0003c0003t0009g0324 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.588+12180A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219134500 | ||||||
chr2:219134670
|
C | T | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+12010G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219134670 | ||||||
chr2:219134780
|
T | C | 116 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(113): Show | 116 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.588+11900A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219134780 | ||||||
chr2:219134790
|
A | G | 1 | a0001c0001t0010g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588+11890T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219134790 | ||||||
chr2:219134894
|
C | T | 2 | a0001c0001t0023g0152a0001c0001t0023g0153 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.588+11786G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219134894 | ||||||
chr2:219134948
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.588+11732C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219134948 | ||||||
chr2:219134983
|
T | C | 5 | a0001c0001t0004g0054a0001c0001t0004g0057a0001c0001t0004g0058others(2): Show | 5 | NA18998.hp1 NA19004.hp1 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+11697A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219134983 | ||||||
chr2:219135014
|
G | A | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.588+11666C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135014 | ||||||
chr2:219135043
|
T | TA | 74 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(71): Show | 76 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.588+11636dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135043 | ||||||
chr2:219135043
|
T | TAAAAAAA others(2): Show |
78 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0189others(75): Show | 83 | HG00140.hp2 HG00408.hp1 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.588+11628_588+1163 others(13): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135043 | ||||||
chr2:219135043
|
T | TAAAAAAA others(3): Show |
105 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0183others(102): Show | 105 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.588+11627_588+1163 others(14): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135043 | ||||||
chr2:219135043
|
T | TAAAAAAA others(4): Show |
9 | a0001c0001t0002g0035a0001c0001t0002g0046a0001c0001t0002g0064others(6): Show | 9 | HG02148.hp2 HG02615.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.588+11626_588+1163 others(15): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135043 | ||||||
chr2:219135043
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0038g0156 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.588+11625_588+1163 others(16): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135043 | ||||||
chr2:219135137
|
A | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0307 | 2 | HG00673.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.588+11543T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135137 | ||||||
chr2:219135219
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.588+11461C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135219 | ||||||
chr2:219135222
|
G | A | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.588+11458C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135222 | ||||||
chr2:219135329
|
G | A | 7 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.588+11351C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135329 | ||||||
chr2:219135539
|
G | T | 1 | a0001c0001t0002g0096 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.588+11141C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135539 | ||||||
chr2:219135576
|
T | C | 6 | a0002c0002t0006g0146a0002c0002t0006g0147a0002c0002t0006g0148others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+11104A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135576 | ||||||
chr2:219135755
|
T | C | 13 | a0001c0001t0049g0343a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.588+10925A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135755 | ||||||
chr2:219135795
|
T | C | 3 | a0001c0001t0002g0109a0001c0001t0002g0110a0001c0001t0002g0113 | 3 | NA18957.hp2 NA19012.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.588+10885A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135795 | ||||||
chr2:219135994
|
G | C | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+10686C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219135994 | ||||||
chr2:219136119
|
C | T | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+10561G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136119 | ||||||
chr2:219136140
|
A | G | 9 | a0001c0001t0001g0336a0001c0001t0008g0140a0001c0001t0008g0141others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+10540T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136140 | ||||||
chr2:219136286
|
C | CT | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0233others(4): Show | 7 | HG00673.hp1 HG01346.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.588+10393dupA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136286 | ||||||
chr2:219136286
|
CT | C | 133 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0204others(130): Show | 133 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.588+10393delA | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136286 | ||||||
chr2:219136286
|
CTT | C | 68 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0182others(65): Show | 72 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.588+10392_588+1039 others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136286 | ||||||
chr2:219136336
|
T | G | 2 | a0001c0001t0005g0055a0001c0001t0041g0056 | 2 | HG01192.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.588+10344A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136336 | ||||||
chr2:219136465
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588+10215A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136465 | ||||||
chr2:219136509
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.588+10171C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136509 | ||||||
chr2:219136582
|
C | T | 2 | a0002c0002t0006g0148a0002c0002t0006g0149 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.588+10098G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136582 | ||||||
chr2:219136596
|
G | A | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+10084C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136596 | ||||||
chr2:219136706
|
G | A | 5 | a0001c0001t0009g0326a0001c0001t0009g0327a0003c0003t0009g0322others(2): Show | 5 | HG01175.hp2 HG01975.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+9974C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136706 | ||||||
chr2:219136805
|
G | A | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+9875C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219136805 | ||||||
chr2:219137071
|
GA | G | 10 | a0001c0001t0001g0253a0001c0001t0001g0273a0001c0001t0001g0311others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.588+9608delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137071 | ||||||
chr2:219137100
|
C | G | 1 | a0001c0001t0001g0325 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.588+9580G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137100 | ||||||
chr2:219137482
|
C | T | 12 | a0002c0002t0006g0124a0002c0002t0006g0125a0002c0002t0006g0126others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.588+9198G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137482 | ||||||
chr2:219137567
|
A | T | 1 | a0001c0001t0030g0296 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.588+9113T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137567 | ||||||
chr2:219137570
|
C | CA | 9 | a0001c0001t0001g0267a0001c0001t0001g0276a0001c0001t0001g0277others(6): Show | 9 | HG00544.hp1 HG02015.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+9109dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137570 | ||||||
chr2:219137570
|
C | CAAAAAAA | 8 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0033others(5): Show | 8 | HG00558.hp1 HG01981.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+9103_588+9109d others(9): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137570 | ||||||
chr2:219137570
|
C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0029others(12): Show | 15 | HG01106.hp1 HG01928.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+9102_588+9109d others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137570 | ||||||
chr2:219137570
|
CA | C | 122 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(119): Show | 126 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.588+9109delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137570 | ||||||
chr2:219137583
|
A | C | 2 | a0002c0002t0006g0146a0002c0002t0006g0147 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.588+9097T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137583 | ||||||
chr2:219137583
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.588+9087_588+9096d others(12): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137583 | ||||||
chr2:219137584
|
A | C | 6 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342others(3): Show | 6 | HG02280.hp1 HG02647.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+9096T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137584 | ||||||
chr2:219137589
|
A | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0297a0001c0001t0045g0200 | 3 | NA18977.hp2 NA19004.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.588+9091T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137589 | ||||||
chr2:219137592
|
AC | A | 9 | a0001c0001t0001g0315a0001c0001t0002g0087a0001c0001t0008g0140others(6): Show | 10 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.588+9087delG | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137592 | ||||||
chr2:219137593
|
C | A | 103 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0266others(100): Show | 103 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.588+9087G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137593 | ||||||
chr2:219137595
|
A | AAAAAAAA others(2): Show |
6 | a0001c0001t0004g0070a0001c0001t0004g0075a0001c0001t0004g0082others(3): Show | 6 | HG00609.hp1 NA18940.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+9084_588+9085i others(11): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137595 | ||||||
chr2:219137595
|
A | AAAAAAAA others(1): Show |
26 | a0001c0001t0002g0026a0001c0001t0002g0046a0001c0001t0002g0052others(23): Show | 26 | HG00408.hp2 HG00733.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.588+9084_588+9085i others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137595 | ||||||
chr2:219137595
|
A | AAAAAAAC | 40 | a0001c0001t0002g0041a0001c0001t0002g0045a0001c0001t0002g0047others(37): Show | 40 | HG00099.hp2 HG00639.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.588+9078_588+9084d others(9): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137595 | ||||||
chr2:219137595
|
A | C | 3 | a0001c0001t0002g0087a0001c0001t0005g0055a0001c0001t0007g0071 | 3 | HG01192.hp2 HG03225.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.588+9085T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137595 | ||||||
chr2:219137812
|
C | A | 129 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(126): Show | 129 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.588+8868G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137812 | ||||||
chr2:219137826
|
T | C | 1 | a0001c0001t0010g0335 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.588+8854A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219137826 | ||||||
chr2:219138063
|
C | G | 1 | a0001c0001t0001g0302 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.588+8617G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219138063 | ||||||
chr2:219138085
|
A | G | 1 | a0001c0001t0010g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588+8595T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219138085 | ||||||
chr2:219138090
|
A | C | 116 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(113): Show | 116 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.588+8590T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219138090 | ||||||
chr2:219138112
|
T | G | 201 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0132others(198): Show | 206 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.588+8568A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219138112 | ||||||
chr2:219138166
|
G | C | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0027g0211 | 3 | NA18974.hp2 NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.588+8514C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219138166 | ||||||
chr2:219138519
|
T | A | 116 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(113): Show | 116 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.588+8161A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219138519 | ||||||
chr2:219138666
|
A | T | 1 | a0001c0001t0001g0308 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.588+8014T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219138666 | ||||||
chr2:219138780
|
T | C | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.588+7900A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219138780 | ||||||
chr2:219139011
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.588+7669A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139011 | ||||||
chr2:219139128
|
C | G | 1 | a0001c0001t0025g0010 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.588+7552G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139128 | ||||||
chr2:219139180
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.588+7500G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139180 | ||||||
chr2:219139337
|
C | T | 7 | a0001c0001t0010g0161a0001c0001t0010g0333a0001c0001t0010g0334others(4): Show | 8 | HG02071.hp2 HG02083.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+7343G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139337 | ||||||
chr2:219139494
|
A | G | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+7186T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139494 | ||||||
chr2:219139521
|
G | A | 190 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0132others(187): Show | 194 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.588+7159C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139521 | ||||||
chr2:219139538
|
C | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+7142G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139538 | ||||||
chr2:219139666
|
G | T | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+7014C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139666 | ||||||
chr2:219139723
|
C | G | 1 | a0001c0001t0004g0070 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.588+6957G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139723 | ||||||
chr2:219139758
|
G | A | 3 | a0001c0001t0011g0330a0001c0001t0011g0331a0001c0001t0011g0332 | 3 | HG02109.hp2 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.588+6922C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139758 | ||||||
chr2:219139780
|
C | T | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(2): Show | 5 | NA18956.hp1 NA19012.hp2 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+6900G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139780 | ||||||
chr2:219139909
|
G | C | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+6771C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139909 | ||||||
chr2:219139947
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.588+6733C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139947 | ||||||
chr2:219139954
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+6726G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219139954 | ||||||
chr2:219140002
|
TG | T | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+6677delC | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219140002 | ||||||
chr2:219140177
|
A | G | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+6503T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219140177 | ||||||
chr2:219140229
|
T | G | 6 | a0002c0002t0006g0124a0002c0002t0006g0125a0002c0002t0006g0126others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+6451A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219140229 | ||||||
chr2:219140242
|
G | A | 6 | a0002c0002t0006g0124a0002c0002t0006g0125a0002c0002t0006g0126others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+6438C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219140242 | ||||||
chr2:219140586
|
T | C | 118 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(115): Show | 121 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.588+6094A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219140586 | ||||||
chr2:219140643
|
A | C | 1 | a0001c0001t0007g0317 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.588+6037T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219140643 | ||||||
chr2:219140689
|
A | G | 47 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(44): Show | 50 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.588+5991T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219140689 | ||||||
chr2:219140806
|
C | T | 2 | a0001c0001t0003g0184a0001c0001t0003g0281 | 2 | HG00558.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.588+5874G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219140806 | ||||||
chr2:219140859
|
T | A | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.588+5821A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219140859 | ||||||
chr2:219140889
|
G | A | 1 | a0001c0001t0032g0198 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.588+5791C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219140889 | ||||||
chr2:219141169
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | NA18991.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.588+5511G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141169 | ||||||
chr2:219141236
|
T | C | 117 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(114): Show | 117 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.588+5444A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141236 | ||||||
chr2:219141334
|
T | C | 11 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0008g0140others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+5346A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141334 | ||||||
chr2:219141379
|
C | CAAAAAAA others(324): Show |
1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588+5300_588+5301i others(333): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141379 | ||||||
chr2:219141379
|
C | CAAAAAAA others(320): Show |
5 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+5300_588+5301i others(329): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141379 | ||||||
chr2:219141379
|
C | CAAAAAAA others(321): Show |
2 | a0001c0001t0008g0145a0001c0001t0047g0328 | 2 | HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.588+5300_588+5301i others(330): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141379 | ||||||
chr2:219141396
|
G | C | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+5284C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141396 | ||||||
chr2:219141400
|
G | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0228 | 2 | HG00733.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.588+5280C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141400 | ||||||
chr2:219141408
|
G | A | 62 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0182others(59): Show | 67 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.588+5272C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141408 | ||||||
chr2:219141430
|
A | G | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.588+5250T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141430 | ||||||
chr2:219141450
|
A | G | 114 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(111): Show | 114 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.588+5230T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141450 | ||||||
chr2:219141634
|
A | G | 13 | a0001c0001t0049g0343a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.588+5046T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141634 | ||||||
chr2:219141861
|
C | T | 114 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(111): Show | 114 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.588+4819G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141861 | ||||||
chr2:219141865
|
G | C | 3 | a0001c0001t0011g0330a0001c0001t0011g0331a0001c0001t0011g0332 | 3 | HG02109.hp2 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.588+4815C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141865 | ||||||
chr2:219141922
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.588+4758G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219141922 | ||||||
chr2:219142210
|
G | T | 2 | a0001c0001t0001g0283a0001c0001t0001g0314 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.588+4470C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142210 | ||||||
chr2:219142210
|
GGAAGA | G | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0252others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.588+4465_588+4469d others(7): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142210 | ||||||
chr2:219142277
|
C | A | 1 | a0001c0001t0003g0196 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.588+4403G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142277 | ||||||
chr2:219142414
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588+4266C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142414 | ||||||
chr2:219142477
|
C | A | 1 | a0001c0001t0003g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.588+4203G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142477 | ||||||
chr2:219142593
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+4087G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142593 | ||||||
chr2:219142646
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.588+4034T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142646 | ||||||
chr2:219142669
|
A | G | 3 | a0001c0001t0023g0152a0001c0001t0023g0153a0001c0001t0044g0154 | 3 | HG02280.hp1 HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.588+4011T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142669 | ||||||
chr2:219142692
|
C | T | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.588+3988G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142692 | ||||||
chr2:219142782
|
T | C | 3 | a0001c0001t0023g0152a0001c0001t0023g0153a0001c0001t0044g0154 | 3 | HG02280.hp1 HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.588+3898A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142782 | ||||||
chr2:219142973
|
C | T | 1 | a0001c0001t0044g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.588+3707G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219142973 | ||||||
chr2:219143055
|
C | G | 1 | a0001c0001t0001g0289 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.588+3625G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219143055 | ||||||
chr2:219143112
|
C | T | 10 | a0001c0001t0003g0171a0001c0001t0003g0196a0001c0001t0008g0140others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.588+3568G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219143112 | ||||||
chr2:219143130
|
C | T | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+3550G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219143130 | ||||||
chr2:219143171
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0306 | 2 | HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.588+3509A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219143171 | ||||||
chr2:219143391
|
C | T | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.588+3289G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219143391 | ||||||
chr2:219143452
|
A | G | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+3228T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219143452 | ||||||
chr2:219143600
|
A | G | 9 | a0001c0001t0003g0181a0001c0001t0008g0140a0001c0001t0008g0141others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+3080T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219143600 | ||||||
chr2:219143815
|
G | A | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.588+2865C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219143815 | ||||||
chr2:219143939
|
G | A | 1 | a0001c0001t0003g0136 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.588+2741C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219143939 | ||||||
chr2:219143994
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.588+2686G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219143994 | ||||||
chr2:219144544
|
G | A | 8 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+2136C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219144544 | ||||||
chr2:219144656
|
G | A | 6 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342others(3): Show | 6 | HG02280.hp1 HG02647.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+2024C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219144656 | ||||||
chr2:219144665
|
T | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2015A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219144665 | ||||||
chr2:219144895
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.588+1785C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219144895 | ||||||
chr2:219144943
|
G | A | 118 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(115): Show | 121 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.588+1737C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219144943 | ||||||
chr2:219145188
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.588+1492G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145188 | ||||||
chr2:219145213
|
C | T | 6 | a0001c0001t0002g0023a0001c0001t0002g0097a0001c0001t0002g0099others(3): Show | 6 | HG00099.hp2 HG01123.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+1467G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145213 | ||||||
chr2:219145221
|
A | AAAC | 3 | a0001c0001t0001g0300a0001c0001t0001g0306a0001c0001t0049g0343 | 3 | HG03225.hp1 NA19088.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.588+1456_588+1458d others(5): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145221 | ||||||
chr2:219145221
|
AAAC | A | 89 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0182others(86): Show | 93 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.588+1456_588+1458d others(5): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145221 | ||||||
chr2:219145376
|
C | G | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.588+1304G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145376 | ||||||
chr2:219145492
|
C | T | 10 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0008g0140others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.588+1188G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145492 | ||||||
chr2:219145688
|
C | T | 1 | a0001c0001t0048g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.588+992G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145688 | ||||||
chr2:219145712
|
C | T | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588+968G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145712 | ||||||
chr2:219145942
|
T | TA | 10 | a0001c0001t0001g0240a0001c0001t0001g0306a0001c0001t0008g0140others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.588+737dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145942 | ||||||
chr2:219145942
|
TA | T | 7 | a0001c0001t0001g0210a0001c0001t0001g0273a0001c0001t0002g0038others(4): Show | 7 | HG01346.hp2 HG01496.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.588+737delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145942 | ||||||
chr2:219145949
|
A | T | 1 | a0001c0001t0001g0222 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.588+731T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219145949 | ||||||
chr2:219146138
|
G | A | 12 | a0002c0002t0006g0124a0002c0002t0006g0125a0002c0002t0006g0126others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.588+542C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219146138 | ||||||
chr2:219146161
|
A | G | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.588+519T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219146161 | ||||||
chr2:219146198
|
T | C | 2 | a0001c0001t0026g0167a0001c0001t0029g0203 | 2 | HG01169.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.588+482A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219146198 | ||||||
chr2:219146282
|
C | T | 1 | a0001c0001t0003g0192 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.588+398G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219146282 | ||||||
chr2:219146359
|
T | C | 1 | a0001c0001t0002g0037 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.588+321A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219146359 | ||||||
chr2:219146369
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.588+311G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219146369 | ||||||
chr2:219146370
|
A | C | 59 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(56): Show | 64 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.588+310T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219146370 | ||||||
chr2:219146625
|
C | A | 3 | a0001c0001t0001g0040a0001c0001t0002g0031a0001c0001t0002g0035 | 3 | HG01928.hp2 HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.588+55G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 5/7 | chr2 | 219146625 | ||||||
chr2:219146815
|
A | T | 1 | a0001c0001t0002g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.530-77T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 4/7 | chr2 | 219146815 | ||||||
chr2:219146889
|
G | A | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.530-151C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 4/7 | chr2 | 219146889 | ||||||
chr2:219147228
|
C | CCAGCACT others(21): Show |
1 | a0001c0001t0001g0013 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.529+401_529+428dup others(28): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 4/7 | chr2 | 219147228 | ||||||
chr2:219147263
|
T | C | 3 | a0001c0001t0014g0076a0001c0001t0014g0085a0001c0001t0014g0086 | 3 | HG02015.hp2 NA18965.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.529+394A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 4/7 | chr2 | 219147263 | ||||||
chr2:219147311
|
C | G | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.529+346G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 4/7 | chr2 | 219147311 | ||||||
chr2:219147394
|
C | A | 342 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(339): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.529+263G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 4/7 | chr2 | 219147394 | ||||||
chr2:219147395
|
T | A | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.529+262A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 4/7 | chr2 | 219147395 | ||||||
chr2:219147408
|
C | T | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.529+249G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 4/7 | chr2 | 219147408 | ||||||
chr2:219147854
|
G | C | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.391-59C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219147854 | ||||||
chr2:219147968
|
T | C | 1 | a0001c0001t0034g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.391-173A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219147968 | ||||||
chr2:219148054
|
T | C | 6 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342others(3): Show | 6 | HG02280.hp1 HG02647.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-259A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148054 | ||||||
chr2:219148070
|
C | A | 1 | a0001c0001t0003g0338 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.391-275G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148070 | ||||||
chr2:219148089
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0002g0288 | 2 | NA18983.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.391-294A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148089 | ||||||
chr2:219148399
|
A | T | 6 | a0001c0001t0002g0023a0001c0001t0002g0097a0001c0001t0002g0099others(3): Show | 6 | HG00099.hp2 HG01123.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-604T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148399 | ||||||
chr2:219148542
|
G | A | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.391-747C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148542 | ||||||
chr2:219148590
|
G | A | 4 | a0001c0001t0002g0041a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 4 | HG03239.hp1 HG03688.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-795C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148590 | ||||||
chr2:219148681
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.391-886T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148681 | ||||||
chr2:219148876
|
A | C | 5 | a0001c0001t0004g0054a0001c0001t0004g0057a0001c0001t0004g0058others(2): Show | 5 | NA18998.hp1 NA19004.hp1 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-1081T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148876 | ||||||
chr2:219148882
|
C | A | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.391-1087G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148882 | ||||||
chr2:219148885
|
C | T | 4 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(1): Show | 4 | NA18962.hp2 NA18975.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-1090G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148885 | ||||||
chr2:219148889
|
T | C | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.391-1094A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148889 | ||||||
chr2:219148920
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.391-1125C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148920 | ||||||
chr2:219148939
|
A | G | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.391-1144T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219148939 | ||||||
chr2:219149042
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.391-1247G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149042 | ||||||
chr2:219149317
|
C | T | 3 | a0001c0001t0011g0330a0001c0001t0011g0331a0001c0001t0011g0332 | 3 | HG02109.hp2 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.391-1522G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149317 | ||||||
chr2:219149378
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.391-1583C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149378 | ||||||
chr2:219149431
|
C | T | 3 | a0001c0001t0002g0030a0001c0001t0002g0034a0001c0001t0002g0036 | 3 | NA18949.hp2 NA18961.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.391-1636G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149431 | ||||||
chr2:219149508
|
C | T | 1 | a0001c0001t0005g0165 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.391-1713G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149508 | ||||||
chr2:219149531
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.391-1736C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149531 | ||||||
chr2:219149830
|
G | T | 1 | a0001c0001t0004g0053 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.391-2035C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149830 | ||||||
chr2:219149886
|
G | A | 1 | a0001c0001t0009g0327 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.391-2091C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149886 | ||||||
chr2:219149887
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.391-2092C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149887 | ||||||
chr2:219149898
|
A | G | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-2103T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149898 | ||||||
chr2:219149953
|
C | T | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.391-2158G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219149953 | ||||||
chr2:219150033
|
G | C | 1 | a0001c0001t0005g0021 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.391-2238C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150033 | ||||||
chr2:219150099
|
A | G | 1 | a0001c0001t0019g0243 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.391-2304T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150099 | ||||||
chr2:219150401
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0245 | 2 | NA18944.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.391-2606T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150401 | ||||||
chr2:219150440
|
C | T | 1 | a0001c0001t0027g0211 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.391-2645G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150440 | ||||||
chr2:219150495
|
G | A | 59 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(56): Show | 64 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.391-2700C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150495 | ||||||
chr2:219150558
|
G | A | 1 | a0001c0001t0047g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.391-2763C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150558 | ||||||
chr2:219150600
|
G | A | 1 | a0001c0001t0002g0089 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.391-2805C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150600 | ||||||
chr2:219150681
|
C | T | 1 | a0001c0001t0036g0077 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.391-2886G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150681 | ||||||
chr2:219150787
|
C | G | 1 | a0001c0001t0002g0064 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.391-2992G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150787 | ||||||
chr2:219150841
|
A | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0256 | 2 | NA18950.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.391-3046T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150841 | ||||||
chr2:219150888
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG01243.hp1 HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.391-3093C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150888 | ||||||
chr2:219150933
|
G | C | 58 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(55): Show | 63 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.391-3138C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150933 | ||||||
chr2:219150980
|
T | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0314 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.391-3185A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219150980 | ||||||
chr2:219151127
|
C | CA | 22 | a0001c0001t0001g0208a0001c0001t0001g0235a0001c0001t0001g0262others(19): Show | 22 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.391-3333dupT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219151127 | ||||||
chr2:219151127
|
CA | C | 20 | a0001c0001t0001g0015a0001c0001t0001g0212a0001c0001t0001g0213others(17): Show | 21 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.391-3333delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219151127 | ||||||
chr2:219151208
|
C | T | 59 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(56): Show | 64 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.391-3413G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219151208 | ||||||
chr2:219151357
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0002g0288 | 2 | NA18983.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.391-3562C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219151357 | ||||||
chr2:219151372
|
T | C | 66 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0204others(63): Show | 68 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.391-3577A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219151372 | ||||||
chr2:219151682
|
T | C | 13 | a0001c0004t0001g0155a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.391-3887A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219151682 | ||||||
chr2:219151686
|
A | C | 1 | a0001c0001t0001g0325 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.391-3891T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219151686 | ||||||
chr2:219151729
|
A | G | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.391-3934T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219151729 | ||||||
chr2:219151875
|
C | T | 12 | a0002c0002t0006g0124a0002c0002t0006g0125a0002c0002t0006g0126others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.391-4080G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219151875 | ||||||
chr2:219151999
|
A | C | 1 | a0001c0001t0002g0095 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.391-4204T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219151999 | ||||||
chr2:219152127
|
A | G | 4 | a0001c0001t0011g0330a0001c0001t0011g0331a0001c0001t0011g0332others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-4332T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152127 | ||||||
chr2:219152304
|
G | A | 1 | a0001c0001t0013g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.391-4509C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152304 | ||||||
chr2:219152568
|
C | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-4773G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152568 | ||||||
chr2:219152704
|
C | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+4768G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152704 | ||||||
chr2:219152774
|
C | CATTTATT others(7): Show |
1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+4697_390+4698i others(16): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152774 | ||||||
chr2:219152775
|
A | ATTTATTT others(3): Show |
4 | a0001c0001t0003g0012a0001c0004t0001g0155a0002c0002t0006g0150others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+4687_390+4696d others(12): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152775 | ||||||
chr2:219152779
|
A | ATTTATT | 3 | a0001c0001t0003g0011a0002c0002t0006g0148a0002c0002t0006g0149 | 3 | HG01884.hp2 HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.390+4687_390+4692d others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152779 | ||||||
chr2:219152783
|
A | ATT | 18 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0187others(15): Show | 18 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.390+4687_390+4688d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152783 | ||||||
chr2:219152785
|
TTATTTTT others(5): Show |
T | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.390+4675_390+4686d others(14): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152785 | ||||||
chr2:219152787
|
A | ATATTTAT others(5): Show |
1 | a0001c0001t0001g0287 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.390+4684_390+4685i others(14): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152787 | ||||||
chr2:219152787
|
A | T | 60 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(57): Show | 64 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.390+4685T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152787 | ||||||
chr2:219152789
|
T | A | 61 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(58): Show | 65 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.390+4683A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTA | 26 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0178others(23): Show | 26 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.390+4682_390+4683i others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTATTTTT others(9): Show |
3 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | NA18962.hp2 NA19066.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.390+4682_390+4683i others(18): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTATTTTT others(13): Show |
1 | a0001c0001t0001g0239 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.390+4682_390+4683i others(22): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTTTA | 3 | a0001c0001t0001g0325a0001c0001t0031g0310a0001c0001t0039g0130 | 3 | HG02922.hp2 HG03486.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.390+4679_390+4682d others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTTTATTT others(1): Show |
6 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0218others(3): Show | 6 | HG01169.hp2 HG03831.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+4675_390+4682d others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTTTATTT others(5): Show |
19 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(16): Show | 19 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.390+4671_390+4682d others(14): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTTTATTT others(9): Show |
32 | a0001c0001t0001g0006a0001c0001t0001g0162a0001c0001t0001g0197others(29): Show | 33 | HG00733.hp1 HG01167.hp2 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.390+4667_390+4682d others(18): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTTTATTT others(13): Show |
34 | a0001c0001t0001g0007a0001c0001t0001g0202a0001c0001t0001g0222others(31): Show | 36 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.390+4663_390+4682d others(22): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTTTATTT others(17): Show |
10 | a0001c0001t0001g0227a0001c0001t0001g0246a0001c0001t0001g0247others(7): Show | 10 | HG00642.hp2 HG00673.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.390+4659_390+4682d others(26): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTTTATTT others(21): Show |
3 | a0001c0001t0001g0229a0001c0001t0001g0248a0001c0001t0001g0260 | 3 | HG01993.hp2 HG02074.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.390+4655_390+4682d others(30): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
T | TTTTTTTT others(13): Show |
1 | a0001c0001t0001g0329 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.390+4682_390+4683i others(22): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152789
|
TTTTATTT others(5): Show |
T | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+4671_390+4682d others(14): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152789 | ||||||
chr2:219152929
|
A | G | 1 | a0001c0001t0017g0009 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.390+4543T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152929 | ||||||
chr2:219152945
|
G | C | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+4527C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152945 | ||||||
chr2:219152964
|
G | A | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+4508C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152964 | ||||||
chr2:219152966
|
C | A | 1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.390+4506G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219152966 | ||||||
chr2:219153087
|
G | A | 3 | a0001c0001t0014g0076a0001c0001t0014g0085a0001c0001t0014g0086 | 3 | HG02015.hp2 NA18965.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.390+4385C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153087 | ||||||
chr2:219153244
|
T | C | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(2): Show | 5 | NA18956.hp1 NA19012.hp2 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+4228A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153244 | ||||||
chr2:219153368
|
T | G | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.390+4104A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153368 | ||||||
chr2:219153369
|
A | C | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.390+4103T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153369 | ||||||
chr2:219153567
|
C | T | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0280 | 3 | HG03098.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.390+3905G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153567 | ||||||
chr2:219153568
|
G | A | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.390+3904C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153568 | ||||||
chr2:219153602
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.390+3870T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153602 | ||||||
chr2:219153688
|
GA | G | 49 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0029others(46): Show | 49 | HG00408.hp2 HG00639.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.390+3783delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153688 | ||||||
chr2:219153692
|
A | AG | 59 | a0001c0001t0001g0133a0001c0001t0001g0188a0001c0001t0001g0189others(56): Show | 62 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.390+3779dupC | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153692 | ||||||
chr2:219153692
|
A | AGG | 27 | a0001c0001t0001g0132a0001c0001t0001g0182a0001c0001t0001g0183others(24): Show | 28 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.390+3778_390+3779d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153692 | ||||||
chr2:219153692
|
A | AGGC | 22 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0214others(19): Show | 22 | HG00673.hp1 HG01099.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.390+3779_390+3780i others(5): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153692 | ||||||
chr2:219153692
|
A | AGGGGGGG others(3): Show |
1 | a0001c0001t0008g0141 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.390+3770_390+3779d others(12): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153692 | ||||||
chr2:219153692
|
A | G | 59 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0027others(56): Show | 59 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.390+3780T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153692 | ||||||
chr2:219153693
|
G | GGC | 91 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(88): Show | 94 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.390+3778_390+3779i others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153693 | ||||||
chr2:219153699
|
G | C | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+3773C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153699 | ||||||
chr2:219153702
|
G | C | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | NA18991.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.390+3770C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153702 | ||||||
chr2:219153704
|
T | C | 72 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0027others(69): Show | 72 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.390+3768A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153704 | ||||||
chr2:219153704
|
T | G | 42 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0034others(39): Show | 42 | HG00408.hp2 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.390+3768A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153704 | ||||||
chr2:219153705
|
G | T | 1 | a0001c0001t0039g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.390+3767C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153705 | ||||||
chr2:219153705
|
GGA | G | 66 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0027others(63): Show | 66 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.390+3765_390+3766d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153705 | ||||||
chr2:219153706
|
G | C | 42 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0034others(39): Show | 42 | HG00408.hp2 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.390+3766C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153706 | ||||||
chr2:219153707
|
A | G | 42 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0034others(39): Show | 42 | HG00408.hp2 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.390+3765T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153707 | ||||||
chr2:219153778
|
T | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG01243.hp1 HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.390+3694A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153778 | ||||||
chr2:219153861
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.390+3611C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153861 | ||||||
chr2:219153963
|
A | G | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+3509T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219153963 | ||||||
chr2:219154026
|
A | G | 6 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342others(3): Show | 6 | HG02280.hp1 HG02647.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+3446T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154026 | ||||||
chr2:219154118
|
A | G | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+3354T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154118 | ||||||
chr2:219154124
|
A | T | 12 | a0002c0002t0006g0124a0002c0002t0006g0125a0002c0002t0006g0126others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.390+3348T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154124 | ||||||
chr2:219154186
|
G | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+3286C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154186 | ||||||
chr2:219154192
|
G | A | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.390+3280C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154192 | ||||||
chr2:219154244
|
C | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+3228G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154244 | ||||||
chr2:219154305
|
G | C | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+3167C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154305 | ||||||
chr2:219154306
|
A | G | 59 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(56): Show | 64 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.390+3166T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154306 | ||||||
chr2:219154400
|
C | T | 4 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0218others(1): Show | 4 | HG03831.hp1 NA18974.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+3072G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154400 | ||||||
chr2:219154622
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.390+2850A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154622 | ||||||
chr2:219154655
|
A | G | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+2817T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154655 | ||||||
chr2:219154659
|
C | T | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.390+2813G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154659 | ||||||
chr2:219154689
|
T | C | 1 | a0001c0001t0012g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.390+2783A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154689 | ||||||
chr2:219154707
|
G | A | 2 | a0001c0001t0018g0219a0001c0001t0018g0220 | 2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.390+2765C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154707 | ||||||
chr2:219154759
|
C | G | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+2713G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154759 | ||||||
chr2:219154762
|
T | C | 196 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0132others(193): Show | 200 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.390+2710A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154762 | ||||||
chr2:219154776
|
G | C | 1 | a0001c0001t0004g0053 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.390+2696C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154776 | ||||||
chr2:219154831
|
T | C | 5 | a0001c0001t0002g0168a0001c0001t0021g0169a0001c0001t0021g0170others(2): Show | 5 | HG01978.hp2 HG02293.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+2641A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154831 | ||||||
chr2:219154885
|
A | C | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.390+2587T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154885 | ||||||
chr2:219154889
|
C | T | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+2583G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154889 | ||||||
chr2:219154916
|
T | C | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.390+2556A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219154916 | ||||||
chr2:219155237
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.390+2235G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219155237 | ||||||
chr2:219155409
|
A | T | 5 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG00099.hp1 HG01099.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+2063T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219155409 | ||||||
chr2:219155533
|
T | C | 1 | a0001c0001t0001g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.390+1939A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219155533 | ||||||
chr2:219155613
|
T | C | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.390+1859A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219155613 | ||||||
chr2:219155698
|
G | C | 1 | a0001c0001t0045g0200 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.390+1774C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219155698 | ||||||
chr2:219155719
|
G | A | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.390+1753C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219155719 | ||||||
chr2:219155954
|
A | T | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.390+1518T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219155954 | ||||||
chr2:219155966
|
C | G | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.390+1506G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219155966 | ||||||
chr2:219156009
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.390+1463C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156009 | ||||||
chr2:219156173
|
C | G | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0280 | 3 | HG03098.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.390+1299G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156173 | ||||||
chr2:219156228
|
GAC | G | 3 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0010g0335 | 3 | HG02071.hp2 HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.390+1242_390+1243d others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156228 | ||||||
chr2:219156257
|
T | A | 1 | a0001c0001t0001g0272 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.390+1215A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156257 | ||||||
chr2:219156296
|
C | T | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1176G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156296 | ||||||
chr2:219156568
|
T | C | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+904A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156568 | ||||||
chr2:219156671
|
C | A | 1 | a0001c0001t0001g0311 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.390+801G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156671 | ||||||
chr2:219156680
|
T | C | 1 | a0001c0001t0004g0022 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.390+792A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156680 | ||||||
chr2:219156756
|
T | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0249a0001c0001t0001g0251others(1): Show | 4 | HG02523.hp1 NA18951.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+716A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156756 | ||||||
chr2:219156766
|
A | G | 3 | a0001c0001t0012g0002a0001c0001t0012g0160a0001c0001t0046g0159 | 4 | HG02109.hp1 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+706T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156766 | ||||||
chr2:219156769
|
T | C | 1 | a0001c0004t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.390+703A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156769 | ||||||
chr2:219156790
|
T | C | 198 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0132others(195): Show | 203 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.390+682A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156790 | ||||||
chr2:219156812
|
T | A | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390+660A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156812 | ||||||
chr2:219156813
|
A | T | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390+659T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156813 | ||||||
chr2:219156980
|
T | A | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390+492A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219156980 | ||||||
chr2:219157045
|
T | C | 1 | a0001c0001t0002g0321 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.390+427A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219157045 | ||||||
chr2:219157047
|
A | C | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390+425T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219157047 | ||||||
chr2:219157074
|
A | G | 58 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(55): Show | 63 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.390+398T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219157074 | ||||||
chr2:219157136
|
T | C | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+336A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219157136 | ||||||
chr2:219157249
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.390+223G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219157249 | ||||||
chr2:219157296
|
T | A | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390+176A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219157296 | ||||||
chr2:219157352
|
A | G | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.390+120T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219157352 | ||||||
chr2:219157407
|
A | C | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390+65T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219157407 | ||||||
chr2:219157454
|
C | T | 319 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(316): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.390+18G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 3/7 | chr2 | 219157454 | ||||||
chr2:219157713
|
G | C | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.178-29C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157713 | ||||||
chr2:219157748
|
C | G | 1 | a0001c0001t0002g0037 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.178-64G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157748 | ||||||
chr2:219157803
|
A | G | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178-119T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157803 | ||||||
chr2:219157804
|
G | A | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178-120C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157804 | ||||||
chr2:219157805
|
A | G | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178-121T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157805 | ||||||
chr2:219157826
|
G | A | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178-142C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157826 | ||||||
chr2:219157827
|
A | G | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178-143T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157827 | ||||||
chr2:219157968
|
T | G | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.177+218A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157968 | ||||||
chr2:219157971
|
T | C | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.177+215A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157971 | ||||||
chr2:219157972
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.177+214A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157972 | ||||||
chr2:219157987
|
TCTCTCAC others(3): Show |
T | 1 | a0001c0001t0004g0054 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.177+189_177+198del others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157987 | ||||||
chr2:219157989
|
T | A | 1 | a0001c0001t0001g0312 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.177+197A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157989 | ||||||
chr2:219157989
|
TCTCA | T | 3 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0095 | 3 | HG02735.hp2 NA18974.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.177+193_177+196del others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157989 | ||||||
chr2:219157989
|
TCTCACA | T | 22 | a0001c0001t0001g0040a0001c0001t0001g0228a0001c0001t0002g0037others(19): Show | 22 | HG00733.hp2 HG01074.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.177+191_177+196del others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157989 | ||||||
chr2:219157989
|
TCTCACAC others(1): Show |
T | 71 | a0001c0001t0001g0084a0001c0001t0002g0023a0001c0001t0002g0026others(68): Show | 71 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.177+189_177+196del others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157989 | ||||||
chr2:219157989
|
TCTCACAC others(3): Show |
T | 1 | a0001c0001t0002g0065 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.177+187_177+196del others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157989 | ||||||
chr2:219157989
|
TCTCACAC others(5): Show |
T | 1 | a0001c0001t0002g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.177+185_177+196del others(12): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157989 | ||||||
chr2:219157991
|
T | A | 3 | a0001c0001t0001g0309a0001c0001t0001g0312a0001c0001t0002g0119 | 3 | HG02698.hp2 HG03017.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.177+195A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157991 | ||||||
chr2:219157991
|
T | TCA | 4 | a0001c0001t0001g0311a0001c0001t0001g0314a0001c0001t0001g0325others(1): Show | 4 | HG02738.hp1 HG02922.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+193_177+194dup others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157991 | ||||||
chr2:219157991
|
T | TCACACAC others(5): Show |
1 | a0001c0001t0001g0265 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.177+183_177+194dup others(12): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157991 | ||||||
chr2:219157991
|
TCA | T | 45 | a0001c0001t0001g0162a0001c0001t0001g0182a0001c0001t0001g0183others(42): Show | 46 | HG00558.hp2 HG00733.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.177+193_177+194del others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157991 | ||||||
chr2:219157991
|
TCACA | T | 42 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0001g0133others(39): Show | 43 | HG01099.hp2 HG01175.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.177+191_177+194del others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157991 | ||||||
chr2:219157991
|
TCACACA | T | 105 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(102): Show | 107 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.177+189_177+194del others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157991 | ||||||
chr2:219157991
|
TCACACAC others(1): Show |
T | 13 | a0001c0001t0001g0227a0001c0001t0001g0297a0001c0001t0002g0041others(10): Show | 13 | HG02109.hp2 HG02293.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+187_177+194del others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157991 | ||||||
chr2:219157991
|
TCACACAC others(3): Show |
T | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.177+185_177+194del others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157991 | ||||||
chr2:219157991
|
TCACACAC others(17): Show |
T | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.177+171_177+194del others(24): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157991 | ||||||
chr2:219157993
|
A | T | 19 | a0001c0001t0001g0195a0001c0001t0003g0003a0001c0001t0003g0004others(16): Show | 21 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.177+193T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157993 | ||||||
chr2:219157995
|
A | T | 43 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(40): Show | 46 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.177+191T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157995 | ||||||
chr2:219157997
|
A | T | 42 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(39): Show | 44 | HG00558.hp2 HG01243.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.177+189T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157997 | ||||||
chr2:219157999
|
A | T | 23 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(20): Show | 24 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.177+187T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219157999 | ||||||
chr2:219158001
|
A | T | 3 | a0001c0001t0002g0064a0001c0001t0003g0163a0001c0001t0034g0139 | 3 | HG02717.hp2 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.177+185T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219158001 | ||||||
chr2:219158003
|
A | T | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.177+183T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219158003 | ||||||
chr2:219158022
|
CACACACA others(11): Show |
C | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.177+146_177+163del others(18): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219158022 | ||||||
chr2:219158100
|
G | A | 4 | a0001c0001t0002g0313a0001c0001t0003g0278a0001c0001t0003g0279others(1): Show | 4 | HG03098.hp1 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+86C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 2/7 | chr2 | 219158100 | ||||||
chr2:219158456
|
T | G | 1 | a0001c0001t0038g0156 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1-94A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158456 | ||||||
chr2:219158474
|
A | C | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1-112T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158474 | ||||||
chr2:219158509
|
C | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0297 | 2 | NA19004.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1-147G>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158509 | ||||||
chr2:219158567
|
T | G | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1-205A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158567 | ||||||
chr2:219158683
|
C | T | 1 | a0001c0001t0034g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1-321G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158683 | ||||||
chr2:219158780
|
T | A | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-418A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158780 | ||||||
chr2:219158781
|
T | G | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1-419A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158781 | ||||||
chr2:219158792
|
A | C | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1-430T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158792 | ||||||
chr2:219158881
|
TA | T | 3 | a0001c0001t0002g0096a0001c0001t0003g0196a0001c0001t0007g0316 | 3 | NA18951.hp1 NA19005.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1-520delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158881 | ||||||
chr2:219158882
|
A | T | 183 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0132others(180): Show | 187 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1-520T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158882 | ||||||
chr2:219158954
|
T | C | 1 | a0001c0001t0003g0338 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1-592A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219158954 | ||||||
chr2:219159041
|
A | C | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1-679T>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159041 | ||||||
chr2:219159222
|
G | C | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1-860C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159222 | ||||||
chr2:219159335
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1-973A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159335 | ||||||
chr2:219159339
|
G | C | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1-977C>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159339 | ||||||
chr2:219159513
|
T | TTATA | 93 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(90): Show | 93 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1-1155_1-1152dupTA others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159513 | ||||||
chr2:219159513
|
T | TTATATA | 3 | a0001c0001t0006g0098a0001c0001t0016g0104a0001c0001t0016g0105 | 3 | HG02257.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1-1157_1-1152dupTA others(4): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159513 | ||||||
chr2:219159513
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0011g0331 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1-1165_1-1152dupTG others(12): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159513 | ||||||
chr2:219159514
|
T | TATATATA others(59): Show |
1 | a0001c0001t0001g0282 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1-1153_1-1152insGC others(64): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159514 | ||||||
chr2:219159514
|
T | TATATATA others(65): Show |
1 | a0001c0001t0001g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1-1153_1-1152insGC others(70): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159514 | ||||||
chr2:219159514
|
TATATATA others(55): Show |
T | 1 | a0001c0001t0038g0156 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-1+1144_1-1153delG others(61): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159514 | ||||||
chr2:219159516
|
T | TATATATA others(5): Show |
6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-1155_1-1154insGC others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159516 | ||||||
chr2:219159516
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1-1164_1-1155delGC others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159516 | ||||||
chr2:219159518
|
TATATATG others(1): Show |
T | 9 | a0001c0001t0002g0033a0001c0001t0002g0061a0001c0001t0004g0054others(6): Show | 9 | HG01192.hp2 HG02027.hp1 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.1-1164_1-1157delGC others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159518 | ||||||
chr2:219159526
|
C | CAT | 68 | a0001c0001t0001g0134a0001c0001t0001g0182a0001c0001t0001g0183others(65): Show | 71 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1-1166_1-1165dupAT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159526 | ||||||
chr2:219159526
|
C | CATATATA others(9): Show |
5 | a0001c0001t0001g0202a0001c0001t0003g0201a0001c0001t0003g0281others(2): Show | 5 | HG00099.hp1 HG02155.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-1165_1-1164insAT others(14): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159526 | ||||||
chr2:219159526
|
C | CATATATA others(23): Show |
2 | a0001c0001t0017g0008a0001c0001t0017g0009 | 2 | NA18992.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1-1165_1-1164insAT others(28): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159526 | ||||||
chr2:219159526
|
C | CATATATA others(47): Show |
2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG00639.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1-1165_1-1164insAT others(52): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159526 | ||||||
chr2:219159526
|
C | CATATATA others(85): Show |
1 | a0001c0001t0001g0300 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1-1165_1-1164insAT others(90): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159526 | ||||||
chr2:219159526
|
C | CATATATA others(35): Show |
1 | a0001c0001t0001g0240 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1-1165_1-1164insAT others(40): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159526 | ||||||
chr2:219159526
|
C | CATATATA others(73): Show |
1 | a0001c0001t0001g0241 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1-1165_1-1164insAT others(78): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159526 | ||||||
chr2:219159526
|
C | CATATATA others(73): Show |
7 | a0001c0001t0001g0289a0001c0001t0001g0291a0001c0001t0001g0292others(4): Show | 7 | NA18941.hp2 NA18942.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1-1165_1-1164insAT others(78): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159526 | ||||||
chr2:219159526
|
C | CATATATA others(71): Show |
1 | a0001c0001t0001g0297 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1-1165_1-1164insAT others(76): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159526 | ||||||
chr2:219159528
|
T | TATATATA others(5): Show |
38 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0029others(35): Show | 38 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1-1167_1-1166insGC others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159528 | ||||||
chr2:219159528
|
T | TATATATA others(41): Show |
1 | a0001c0001t0005g0032 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1-1167_1-1166insGC others(46): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159528 | ||||||
chr2:219159528
|
T | TATATATA others(29): Show |
2 | a0001c0001t0002g0023a0001c0001t0002g0041 | 2 | HG02602.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-1167_1-1166insGC others(34): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159528 | ||||||
chr2:219159528
|
TATATATA others(29): Show |
T | 11 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0162others(8): Show | 12 | HG00733.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+1156_1-1167delG others(35): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159528 | ||||||
chr2:219159528
|
TATATATA others(41): Show |
T | 3 | a0001c0001t0003g0157a0001c0001t0003g0158a0001c0001t0049g0343 | 3 | NA18963.hp2 NA18995.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-1+1144_1-1167delG others(47): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159528 | ||||||
chr2:219159536
|
TGC | T | 51 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0034others(48): Show | 51 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1-1176_1-1175delGC | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159536 | ||||||
chr2:219159538
|
C | CATATATA others(47): Show |
1 | a0001c0001t0001g0246 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1-1177_1-1176insAT others(52): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159538 | ||||||
chr2:219159538
|
CAT | C | 14 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(11): Show | 14 | HG01891.hp1 HG02055.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1-1178_1-1177delAT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159538 | ||||||
chr2:219159540
|
T | TATATATA others(103): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-1+1179_1-1178insG others(109): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159540 | ||||||
chr2:219159540
|
T | TATATATA others(115): Show |
1 | a0001c0001t0001g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-1+1179_1-1178insG others(121): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159540 | ||||||
chr2:219159540
|
T | TATATATA others(73): Show |
2 | a0001c0001t0007g0316a0001c0001t0007g0317 | 2 | NA18964.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-1+1179_1-1178insG others(79): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159540 | ||||||
chr2:219159540
|
T | TATATATA others(101): Show |
1 | a0001c0001t0001g0016 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-1+1179_1-1178insG others(107): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159540 | ||||||
chr2:219159540
|
T | TATATATA others(45): Show |
1 | a0001c0001t0001g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1+1179_1-1178insG others(51): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159540 | ||||||
chr2:219159540
|
T | TATATATA others(43): Show |
5 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0311others(2): Show | 5 | HG03017.hp2 HG03239.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+1179_1-1178insG others(49): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159540 | ||||||
chr2:219159540
|
T | TATATATA others(15): Show |
4 | a0001c0001t0001g0325a0003c0003t0009g0322a0003c0003t0009g0323others(1): Show | 4 | HG01975.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+1179_1-1178insG others(21): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159540 | ||||||
chr2:219159540
|
T | TATATATA others(27): Show |
1 | a0001c0001t0001g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-1+1179_1-1178insG others(33): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159540 | ||||||
chr2:219159540
|
T | TATATATA others(39): Show |
2 | a0001c0001t0009g0326a0001c0001t0009g0327 | 2 | HG01175.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-1+1179_1-1178insG others(45): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159540 | ||||||
chr2:219159540
|
T | TATATATA others(63): Show |
1 | a0001c0001t0001g0314 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-1+1179_1-1178insG others(69): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159540 | ||||||
chr2:219159541
|
A | G | 51 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0034others(48): Show | 51 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-1+1179T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159541 | ||||||
chr2:219159542
|
T | C | 51 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0034others(48): Show | 51 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-1+1178A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159542 | ||||||
chr2:219159542
|
T | TATATATG others(1): Show |
3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0280 | 3 | HG03098.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-1+1177_-1+1178ins others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159542 | ||||||
chr2:219159542
|
T | TATATGCA others(57): Show |
1 | a0001c0001t0002g0115 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-1+1177_-1+1178ins others(64): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159542 | ||||||
chr2:219159547
|
A | G | 4 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0043others(1): Show | 4 | HG01099.hp1 HG01981.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+1173T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159547 | ||||||
chr2:219159548
|
T | C | 4 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0043others(1): Show | 4 | HG01099.hp1 HG01981.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+1172A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159548 | ||||||
chr2:219159549
|
A | G | 6 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(3): Show | 6 | HG02630.hp1 HG02738.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+1171T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159549 | ||||||
chr2:219159550
|
T | C | 6 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(3): Show | 6 | HG02630.hp1 HG02738.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+1170A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159550 | ||||||
chr2:219159551
|
G | A | 10 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(7): Show | 10 | HG01099.hp1 HG01981.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1+1169C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159551 | ||||||
chr2:219159552
|
C | CAT | 49 | a0001c0001t0001g0134a0001c0001t0001g0202a0001c0001t0001g0208others(46): Show | 49 | HG00099.hp1 HG00639.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.-1+1166_-1+1167dup others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(9): Show |
6 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(3): Show | 6 | HG01346.hp1 HG03486.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(16): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(79): Show |
1 | a0001c0001t0001g0257 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(86): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(81): Show |
1 | a0001c0001t0001g0287 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(88): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(65): Show |
2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | NA18968.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(72): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(81): Show |
1 | a0001c0001t0001g0284 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(88): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(77): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0258 | 5 | HG01106.hp2 HG01192.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(84): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(117): Show |
1 | a0001c0001t0001g0259 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(124): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(35): Show |
1 | a0001c0001t0001g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(42): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(77): Show |
2 | a0001c0001t0001g0305a0001c0001t0001g0337 | 2 | HG02015.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(84): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(63): Show |
4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0303others(1): Show | 4 | NA18943.hp1 NA18965.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(70): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(77): Show |
4 | a0001c0001t0001g0204a0001c0001t0001g0249a0001c0001t0001g0251others(1): Show | 4 | HG02523.hp1 NA18951.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(84): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(119): Show |
1 | a0001c0001t0001g0266 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(126): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(103): Show |
1 | a0001c0001t0001g0336 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(110): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(75): Show |
1 | a0001c0001t0001g0227 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(82): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(61): Show |
1 | a0001c0001t0001g0261 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(68): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(61): Show |
2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00544.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(68): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(73): Show |
2 | a0001c0001t0001g0229a0001c0001t0001g0307 | 2 | HG00673.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(80): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(73): Show |
1 | a0001c0001t0001g0260 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(80): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(77): Show |
1 | a0001c0001t0001g0285 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(84): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(75): Show |
1 | a0001c0001t0001g0267 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(82): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(73): Show |
1 | a0001c0001t0001g0275 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(80): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(77): Show |
1 | a0001c0001t0002g0288 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(84): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(49): Show |
1 | a0001c0001t0030g0296 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(56): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | CATATATA others(43): Show |
1 | a0001c0001t0002g0313 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-1+1167_-1+1168ins others(50): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
C | T | 10 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(7): Show | 10 | HG01099.hp1 HG01981.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1+1168G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
CAT | C | 19 | a0001c0001t0002g0023a0001c0001t0002g0027a0001c0001t0002g0029others(16): Show | 19 | HG00639.hp2 HG01192.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-1+1166_-1+1167del others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159552
|
CATATATA others(7): Show |
C | 1 | a0001c0001t0002g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1+1154_-1+1167del others(14): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159552 | ||||||
chr2:219159554
|
T | TATATATG others(1): Show |
5 | a0001c0001t0002g0116a0001c0001t0002g0118a0001c0001t0002g0120others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+1165_-1+1166ins others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159554 | ||||||
chr2:219159554
|
T | TATATATG others(11): Show |
2 | a0001c0001t0005g0024a0001c0001t0005g0025 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-1+1165_-1+1166ins others(18): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159554 | ||||||
chr2:219159554
|
T | TATATATG others(81): Show |
1 | a0001c0001t0002g0026 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-1+1165_-1+1166ins others(88): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159554 | ||||||
chr2:219159554
|
TATATATA others(3): Show |
T | 4 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0010g0335others(1): Show | 4 | HG02071.hp2 HG02083.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+1156_-1+1165del others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159554 | ||||||
chr2:219159554
|
TATATATA others(15): Show |
T | 21 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(18): Show | 22 | HG00673.hp1 HG00741.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1+1144_-1+1165del others(22): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159554 | ||||||
chr2:219159554
|
TATATATA others(27): Show |
T | 13 | a0001c0004t0001g0155a0002c0002t0006g0124a0002c0002t0006g0125others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+1132_-1+1165del others(34): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159554 | ||||||
chr2:219159558
|
TATATGC | T | 50 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(47): Show | 53 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-1+1156_-1+1161del others(6): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159558 | ||||||
chr2:219159560
|
T | TGC | 11 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(8): Show | 11 | HG02698.hp2 NA18950.hp2 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1+1159_-1+1160ins others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159560 | ||||||
chr2:219159561
|
A | G | 12 | a0001c0001t0002g0041a0001c0001t0002g0100a0001c0001t0002g0101others(9): Show | 12 | HG01123.hp1 HG03139.hp2 NA18522.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+1159T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159561 | ||||||
chr2:219159562
|
T | C | 12 | a0001c0001t0002g0041a0001c0001t0002g0100a0001c0001t0002g0101others(9): Show | 12 | HG01123.hp1 HG03139.hp2 NA18522.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+1158A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159562 | ||||||
chr2:219159563
|
G | A | 68 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0034others(65): Show | 68 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-1+1157C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159563 | ||||||
chr2:219159564
|
C | CAT | 45 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 45 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.-1+1154_-1+1155dup others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159564 | ||||||
chr2:219159564
|
C | CATATATA others(5): Show |
1 | a0001c0001t0011g0331 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+1155_-1+1156ins others(12): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159564 | ||||||
chr2:219159564
|
C | T | 68 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0034others(65): Show | 68 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-1+1156G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159564 | ||||||
chr2:219159564
|
CAT | C | 13 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0061others(10): Show | 13 | HG01192.hp2 HG01981.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+1154_-1+1155del others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159564 | ||||||
chr2:219159565
|
A | G | 45 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0034others(42): Show | 45 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.-1+1155T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159565 | ||||||
chr2:219159566
|
T | C | 45 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0034others(42): Show | 45 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.-1+1154A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159566 | ||||||
chr2:219159566
|
T | TATATATA others(179): Show |
1 | a0001c0001t0013g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1+1153_-1+1154ins others(186): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159566 | ||||||
chr2:219159566
|
T | TATATATG others(1): Show |
13 | a0001c0001t0002g0043a0001c0001t0002g0109a0001c0001t0002g0110others(10): Show | 13 | HG00408.hp2 HG01099.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1+1153_-1+1154ins others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159566 | ||||||
chr2:219159566
|
TATATATA others(3): Show |
T | 4 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG02738.hp2 NA18944.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+1144_-1+1153del others(10): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159566 | ||||||
chr2:219159571
|
A | G | 50 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(47): Show | 53 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-1+1149T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159571 | ||||||
chr2:219159572
|
T | C | 50 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(47): Show | 53 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-1+1148A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159572 | ||||||
chr2:219159574
|
TGC | T | 50 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0188others(47): Show | 53 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-1+1144_-1+1145del others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159574 | ||||||
chr2:219159575
|
G | A | 7 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0004g0022others(4): Show | 7 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+1145C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159575 | ||||||
chr2:219159576
|
C | CAT | 48 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(45): Show | 51 | HG00099.hp1 HG00733.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.-1+1142_-1+1143dup others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159576 | ||||||
chr2:219159576
|
C | CATATATA others(9): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG00140.hp1 HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.-1+1143_-1+1144ins others(16): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159576 | ||||||
chr2:219159576
|
C | CATATATA others(23): Show |
1 | a0001c0001t0001g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-1+1143_-1+1144ins others(30): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159576 | ||||||
chr2:219159576
|
C | CATATATA others(169): Show |
1 | a0001c0001t0001g0228 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-1+1143_-1+1144ins others(176): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159576 | ||||||
chr2:219159576
|
C | T | 7 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0004g0022others(4): Show | 7 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+1144G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159576 | ||||||
chr2:219159576
|
CAT | C | 38 | a0001c0001t0001g0040a0001c0001t0002g0027a0001c0001t0002g0029others(35): Show | 38 | HG00408.hp2 HG01099.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.-1+1142_-1+1143del others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159576 | ||||||
chr2:219159577
|
A | G | 7 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0004g0022others(4): Show | 7 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+1143T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159577 | ||||||
chr2:219159578
|
T | C | 7 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0004g0022others(4): Show | 7 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+1142A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159578
|
T | TATAAATG others(11): Show |
1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-1+1141_-1+1142ins others(18): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159578
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0329 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-1+1141_-1+1142ins others(12): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159578
|
T | TATATATA others(25): Show |
1 | a0001c0001t0002g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-1+1141_-1+1142ins others(32): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159578
|
T | TATATATG others(1): Show |
41 | a0001c0001t0001g0084a0001c0001t0002g0041a0001c0001t0002g0063others(38): Show | 41 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.-1+1141_-1+1142ins others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159578
|
T | TATATATG others(37): Show |
1 | a0001c0001t0004g0053 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-1+1141_-1+1142ins others(44): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159578
|
T | TATATATG others(29): Show |
1 | a0001c0001t0011g0330 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-1+1141_-1+1142ins others(36): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159578
|
T | TATATATG others(35): Show |
2 | a0001c0001t0002g0106a0001c0001t0004g0107 | 2 | HG01123.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-1+1141_-1+1142ins others(42): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159578
|
T | TATATATG others(11): Show |
17 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(14): Show | 17 | NA18522.hp2 NA18941.hp1 NA18943.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1+1141_-1+1142ins others(18): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159578
|
T | TATATATG others(55): Show |
1 | a0001c0001t0002g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-1+1141_-1+1142ins others(62): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159578
|
T | TATATATG others(41): Show |
1 | a0001c0001t0002g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-1+1141_-1+1142ins others(48): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159578 | ||||||
chr2:219159587
|
G | A | 3 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0010g0335 | 3 | HG02071.hp2 HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-1+1133C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159587 | ||||||
chr2:219159588
|
C | CAT | 6 | a0001c0001t0013g0342a0001c0001t0023g0152a0001c0001t0023g0153others(3): Show | 6 | HG02280.hp1 HG02647.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+1130_-1+1131dup others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159588 | ||||||
chr2:219159588
|
C | CATATATA others(229): Show |
1 | a0001c0001t0013g0341 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-1+1131_-1+1132ins others(236): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159588 | ||||||
chr2:219159588
|
C | CATATATA others(235): Show |
1 | a0001c0001t0013g0131 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-1+1131_-1+1132ins others(242): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159588 | ||||||
chr2:219159588
|
C | T | 3 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0010g0335 | 3 | HG02071.hp2 HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-1+1132G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159588 | ||||||
chr2:219159588
|
CAT | C | 4 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0003g0012others(1): Show | 4 | HG02015.hp1 HG02451.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+1130_-1+1131del others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159588 | ||||||
chr2:219159589
|
A | G | 3 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0010g0335 | 3 | HG02071.hp2 HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-1+1131T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159589 | ||||||
chr2:219159590
|
T | C | 3 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0010g0335 | 3 | HG02071.hp2 HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-1+1130A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159590 | ||||||
chr2:219159590
|
T | TATATATA others(37): Show |
1 | a0001c0001t0008g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1+1129_-1+1130ins others(44): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159590 | ||||||
chr2:219159590
|
T | TATATATG others(13): Show |
4 | a0001c0001t0008g0141a0001c0001t0008g0142a0001c0001t0008g0143others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+1129_-1+1130ins others(20): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159590 | ||||||
chr2:219159590
|
T | TATATATG others(35): Show |
1 | a0001c0001t0008g0145 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-1+1129_-1+1130ins others(42): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159590 | ||||||
chr2:219159611
|
A | G | 6 | a0001c0001t0008g0140a0001c0001t0008g0141a0001c0001t0008g0142others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+1109T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159611 | ||||||
chr2:219159618
|
C | T | 113 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(110): Show | 113 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-1+1102G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159618 | ||||||
chr2:219159792
|
C | CCAAA | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-1+927_-1+928insTT others(2): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159792 | ||||||
chr2:219159838
|
T | C | 1 | a0001c0001t0034g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1+882A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159838 | ||||||
chr2:219159919
|
T | C | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-1+801A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159919 | ||||||
chr2:219159928
|
G | T | 106 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.-1+792C>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219159928 | ||||||
chr2:219160047
|
C | T | 1 | a0001c0001t0034g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1+673G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160047 | ||||||
chr2:219160048
|
G | A | 1 | a0001c0001t0034g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1+672C>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160048 | ||||||
chr2:219160049
|
A | T | 1 | a0001c0001t0034g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1+671T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160049 | ||||||
chr2:219160274
|
T | A | 1 | a0001c0001t0003g0338 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-1+446A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160274 | ||||||
chr2:219160285
|
CCCCGCCC others(3): Show |
C | 1 | a0001c0001t0015g0339 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-1+425_-1+434delAC others(8): Show |
NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160285 | ||||||
chr2:219160301
|
T | A | 1 | a0001c0001t0049g0343 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-1+419A>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160301 | ||||||
chr2:219160330
|
CA | C | 4 | a0001c0001t0003g0001a0001c0001t0003g0136a0001c0001t0003g0137others(1): Show | 5 | NA18747.hp2 NA18947.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+389delT | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160330 | ||||||
chr2:219160387
|
T | G | 342 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(339): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.-1+333A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160387 | ||||||
chr2:219160400
|
T | C | 108 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-1+320A>G | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160400 | ||||||
chr2:219160488
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG01243.hp1 HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-1+232G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160488 | ||||||
chr2:219160519
|
A | T | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-1+201T>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160519 | ||||||
chr2:219160521
|
C | A | 1 | a0004c0005t0016g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-1+199G>T | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160521 | ||||||
chr2:219160529
|
T | G | 3 | a0001c0001t0013g0131a0001c0001t0013g0341a0001c0001t0013g0342 | 3 | HG03130.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-1+191A>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160529 | ||||||
chr2:219160541
|
A | G | 8 | a0001c0001t0013g0131a0001c0001t0039g0130a0002c0002t0006g0124others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+179T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160541 | ||||||
chr2:219160586
|
C | T | 105 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0002g0023others(102): Show | 105 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.-1+134G>A | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160586 | ||||||
chr2:219160659
|
A | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+61T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160659 | ||||||
chr2:219160714
|
A | G | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02451.hp1 HG06807.hp2 |
splice_region_variant&intron_variant | LOW | c.-1+6T>C | NHEJ1 | ENSG00000187736.14 | transcript | ENST00000356853.10 | protein_coding | 1/7 | chr2 | 219160714 |