Item | Value |
---|---|
geneid | 471 |
ensemblid | ENSG00000138363.15 |
hgncid | 794 |
symbol | ATIC |
name | 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase |
refseq_nuc | NM_004044.7 |
refseq_prot | NP_004035.2 |
ensembl_nuc | ENST00000236959.14 |
ensembl_prot | ENSP00000236959.9 |
mane_status | MANE Select |
chr | chr2 |
start | 215312059 |
end | 215349764 |
strand | + |
ver | v1.2 |
region | chr2:215312059-215349764 |
region5000 | chr2:215307059-215354764 |
regionname0 | ATIC_chr2_215312059_215349764 |
regionname5000 | ATIC_chr2_215307059_215354764 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 592 | 285 | 78 | 50 | 121 | 6 | 28 | 95 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0002 | 0/0 | 592 | 76 | 2 | 15 | 37 | 4 | 18 | 26 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0003 | 0/0 | 592 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0004 | 0/0 | 592 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0005 | 0/0 | 592 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0006 | 0/0 | 592 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0007 | 0/0 | 592 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0008 | 0/0 | 592 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0009 | 0/0 | 592 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0010 | 0/0 | 592 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0011 | 0/0 | 592 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0012 | 0/0 | 592 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1779 | 278 | 73 | 49 | 121 | 5 | 28 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0002 | 0/0 | 1779 | 74 | 2 | 14 | 36 | 4 | 18 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0003 | 0/0 | 1779 | 7 | 7 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0004 | 0/0 | 1779 | 5 | 4 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0005 | 0/0 | 1779 | 3 | 3 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0006 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0007 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0008 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0009 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0010 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0011 | 0/0 | 1779 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0012 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0013 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0014 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0015 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0016 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0017 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
c0018 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 194 | 202 | 68 | 34 | 78 | 6 | 14 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
t0002 | 0/0 | 194 | 77 | 2 | 11 | 52 | 1 | 11 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
t0003 | 0/0 | 194 | 59 | 0 | 12 | 26 | 3 | 18 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
t0004 | 0/0 | 194 | 21 | 17 | 3 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
t0005 | 0/0 | 194 | 9 | 9 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
t0006 | 0/0 | 194 | 6 | 2 | 3 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
t0007 | 0/0 | 194 | 5 | 0 | 2 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
t0008 | 0/0 | 194 | 2 | 0 | 1 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
t0009 | 0/0 | 194 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 35 | 0 | 6 | 24 | 1 | 4 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0002 | 0/0 | 26 | 0 | 4 | 21 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0003 | 0/0 | 12 | 0 | 3 | 2 | 1 | 6 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0004 | 0/0 | 11 | 10 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0005 | 0/0 | 7 | 1 | 5 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0045 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0218 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1779 | 278 | 73 | 49 | 121 | 5 | 28 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0001c0005 | 0/0 | 1779 | 3 | 3 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0001c0007 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0001c0010 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0001c0011 | 0/0 | 1779 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0002c0002 | 0/0 | 1779 | 74 | 2 | 14 | 36 | 4 | 18 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0002c0014 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0002c0016 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0003c0003 | 0/0 | 1779 | 7 | 7 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0004c0004 | 0/0 | 1779 | 5 | 4 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0005c0006 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0006c0015 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0007c0013 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0008c0012 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0009c0008 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0010c0009 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0011c0017 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 | |
a0012c0018 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1972 | 170 | 49 | 30 | 71 | 5 | 13 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0001t0002 | 0/0 | 1972 | 69 | 2 | 11 | 45 | 0 | 11 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0001t0003 | 0/0 | 1972 | 2 | 0 | 0 | 1 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0001t0004 | 0/0 | 1972 | 21 | 17 | 3 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0001t0005 | 0/0 | 1972 | 4 | 4 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0001t0006 | 0/0 | 1972 | 5 | 1 | 3 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0001t0007 | 0/0 | 1972 | 5 | 0 | 2 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0001t0008 | 0/0 | 1972 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0001t0009 | 0/0 | 1972 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0005t0005 | 0/0 | 1972 | 3 | 3 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0007t0001 | 0/0 | 1972 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0010t0008 | 0/0 | 1972 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0001c0011t0002 | 0/0 | 1972 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0002c0002t0001 | 0/0 | 1972 | 12 | 2 | 2 | 6 | 1 | 1 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0002c0002t0002 | 0/0 | 1972 | 7 | 0 | 0 | 7 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0002c0002t0003 | 0/0 | 1972 | 55 | 0 | 12 | 23 | 3 | 17 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0002c0014t0001 | 0/0 | 1972 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0002c0016t0003 | 0/0 | 1972 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0003c0003t0001 | 0/0 | 1972 | 7 | 7 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0004c0004t0001 | 0/0 | 1972 | 5 | 4 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0005c0006t0005 | 0/0 | 1972 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0006c0015t0003 | 0/0 | 1972 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0007c0013t0001 | 0/0 | 1972 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0008c0012t0001 | 0/0 | 1972 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0009c0008t0001 | 0/0 | 1972 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0010c0009t0001 | 0/0 | 1972 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0011c0017t0006 | 0/0 | 1972 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
a0012c0018t0001 | 0/0 | 1972 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | copy fasta | chr2 | 215307059 | 215354764 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0002 | 0/0 | 25 | 0 | 4 | 20 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0005 | 0/0 | 7 | 1 | 5 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0218 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0001 | 0/0 | 33 | 0 | 6 | 23 | 0 | 4 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0004g0004 | 0/0 | 11 | 10 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0005g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0006g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0006g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0008g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0001t0009g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0005t0005g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0007t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0010t0008g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0001c0011t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0003 | 0/0 | 12 | 0 | 3 | 2 | 1 | 6 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0045 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0014t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0002c0016t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0003c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0003c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0003c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0003c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0003c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0003c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0003c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0004c0004t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0004c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0004c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0004c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0004c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0005c0006t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0005c0006t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0006c0015t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0007c0013t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0008c0012t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0009c0008t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0010c0009t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0011c0017t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
a0012c0018t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0163 | EUR | GBR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00140 | hp2 | a0001 | c0011 | t0002 | g0001 | EUR | GBR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00408 | hp2 | a0002 | c0002 | t0003 | g0044 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00438 | hp2 | a0001 | c0001 | t0007 | g0061 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00544 | hp2 | a0002 | c0002 | t0003 | g0178 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00609 | hp2 | a0006 | c0015 | t0003 | g0176 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00639 | hp2 | a0002 | c0002 | t0003 | g0182 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0027 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01069 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01099 | hp1 | a0002 | c0002 | t0003 | g0190 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01167 | hp1 | a0001 | c0001 | t0006 | g0026 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01167 | hp2 | a0002 | c0002 | t0003 | g0189 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01168 | hp1 | a0002 | c0002 | t0003 | g0202 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0026 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01243 | hp1 | a0004 | c0004 | t0001 | g0207 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01243 | hp2 | a0002 | c0002 | t0003 | g0047 | AMR | PUR | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01256 | hp2 | a0001 | c0010 | t0008 | g0046 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01346 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01358 | hp1 | a0002 | c0002 | t0003 | g0188 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01361 | hp2 | a0002 | c0014 | t0001 | g0179 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01515 | hp1 | a0002 | c0002 | t0003 | g0201 | EUR | IBS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01891 | hp1 | a0001 | c0007 | t0001 | g0040 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0181 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01943 | hp1 | a0001 | c0001 | t0007 | g0058 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01943 | hp2 | a0002 | c0002 | t0003 | g0177 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01978 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01978 | hp2 | a0001 | c0001 | t0007 | g0074 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02015 | hp2 | a0002 | c0002 | t0003 | g0195 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02071 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02080 | hp1 | a0002 | c0002 | t0003 | g0184 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02080 | hp2 | a0002 | c0002 | t0003 | g0095 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02083 | hp1 | a0002 | c0002 | t0003 | g0185 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02145 | hp2 | a0011 | c0017 | t0006 | g0112 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02155 | hp1 | a0002 | c0002 | t0003 | g0044 | EAS | CDX | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | CDX | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CDX | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02257 | hp2 | a0010 | c0009 | t0001 | g0233 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02258 | hp1 | a0004 | c0004 | t0001 | g0210 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02258 | hp2 | a0009 | c0008 | t0001 | g0216 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02293 | hp1 | a0002 | c0002 | t0003 | g0010 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02451 | hp1 | a0003 | c0003 | t0001 | g0217 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02602 | hp1 | a0002 | c0002 | t0003 | g0003 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0111 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02647 | hp1 | a0003 | c0003 | t0001 | g0206 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02683 | hp1 | a0002 | c0002 | t0003 | g0003 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02683 | hp2 | a0002 | c0002 | t0003 | g0197 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02698 | hp1 | a0002 | c0002 | t0003 | g0003 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0097 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02717 | hp2 | a0003 | c0003 | t0001 | g0211 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02723 | hp1 | a0001 | c0007 | t0001 | g0040 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02738 | hp1 | a0002 | c0002 | t0003 | g0170 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02809 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02818 | hp1 | a0003 | c0003 | t0001 | g0212 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02896 | hp1 | a0004 | c0004 | t0001 | g0204 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02897 | hp2 | a0004 | c0004 | t0001 | g0209 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02922 | hp1 | a0008 | c0012 | t0001 | g0049 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02970 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03098 | hp1 | a0003 | c0003 | t0001 | g0205 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03225 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03486 | hp1 | a0012 | c0018 | t0001 | g0048 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03540 | hp2 | a0003 | c0003 | t0001 | g0215 | AFR | GWD | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03669 | hp1 | a0002 | c0002 | t0003 | g0045 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0003 | SAS | STU | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0003 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0187 | SAS | BEB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03834 | hp1 | a0002 | c0002 | t0003 | g0172 | SAS | BEB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03927 | hp1 | a0002 | c0002 | t0003 | g0180 | SAS | BEB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03927 | hp2 | a0002 | c0002 | t0003 | g0199 | SAS | BEB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03942 | hp2 | a0002 | c0002 | t0003 | g0171 | SAS | BEB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG04115 | hp1 | a0001 | c0001 | t0008 | g0016 | SAS | STU | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG04115 | hp2 | a0002 | c0002 | t0003 | g0042 | SAS | STU | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | BEB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG04184 | hp2 | a0002 | c0002 | t0003 | g0042 | SAS | BEB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0038 | SAS | STU | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG04204 | hp2 | a0002 | c0002 | t0003 | g0003 | SAS | STU | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0200 | SAS | STU | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0223 | AFR | YRI | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18747 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | CHB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18906 | hp2 | a0005 | c0006 | t0005 | g0099 | AFR | YRI | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18939 | hp1 | a0002 | c0002 | t0003 | g0043 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18943 | hp2 | a0002 | c0002 | t0003 | g0232 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18948 | hp2 | a0002 | c0002 | t0003 | g0183 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18952 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18965 | hp2 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18967 | hp2 | a0002 | c0002 | t0003 | g0196 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18968 | hp1 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18968 | hp2 | a0001 | c0001 | t0007 | g0069 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18970 | hp2 | a0002 | c0016 | t0003 | g0011 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18971 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18975 | hp2 | a0002 | c0002 | t0003 | g0174 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18977 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18980 | hp2 | a0007 | c0013 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0041 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18991 | hp2 | a0002 | c0002 | t0003 | g0043 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18992 | hp2 | a0002 | c0002 | t0003 | g0041 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19010 | hp2 | a0001 | c0001 | t0007 | g0068 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | LWK | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | LWK | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | LWK | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19057 | hp1 | a0002 | c0002 | t0003 | g0186 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19077 | hp2 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | YRI | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA20129 | hp1 | a0004 | c0004 | t0001 | g0208 | AFR | ASW | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ASW | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA20752 | hp1 | a0002 | c0002 | t0003 | g0003 | EUR | TSI | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0045 | EUR | TSI | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02109 | hp2 | a0003 | c0003 | t0001 | g0214 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG03471 | hp2 | a0005 | c0006 | t0005 | g0100 | AFR | MSL | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0173 | AFR | USA | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | USA | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0098 | AFR | USA | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | USA | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | LWK | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0107 | REF | REF | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0218 | REF | REF | ATIC_chr2_215307059_215354764 | ATIC | chr2 | 215307059 | 215354764 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:215312147 | C | T | 1 | a0012 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.5C>T | p.Ala2Val | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/16 | 89/1972 | 5/1779 | 2/592 | chr2 | 215312147 | ||
chr2:215319722 | A | G | 1 | a0011 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.281A>G | p.Asn94Ser | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/16 | 365/1972 | 281/1779 | 94/592 | chr2 | 215319722 | ||
chr2:215325297 | C | G | 2 | a0002a0006 | 77 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
missense_variant | MODERATE | c.347C>G | p.Thr116Ser | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 5/16 | 431/1972 | 347/1779 | 116/592 | chr2 | 215325297 | ||
chr2:215326885 | A | G | 1 | a0007 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.595A>G | p.Lys199Glu | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/16 | 679/1972 | 595/1779 | 199/592 | chr2 | 215326885 | ||
chr2:215344785 | G | A | 1 | a0004 | 5 | HG01243.hp1 HG02258.hp1 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.1234G>A | p.Glu412Lys | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/16 | 1318/1972 | 1234/1779 | 412/592 | chr2 | 215344785 | ||
chr2:215346848 | T | A | 1 | a0006 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1410T>A | p.His470Gln | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/16 | 1494/1972 | 1410/1779 | 470/592 | chr2 | 215346848 | ||
chr2:215346849 | C | T | 2 | a0003a0004 | 12 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
missense_variant | MODERATE | c.1411C>T | p.Pro471Ser | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/16 | 1495/1972 | 1411/1779 | 471/592 | chr2 | 215346849 | ||
chr2:215346862 | C | T | 1 | a0008 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1424C>T | p.Ser475Leu | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/16 | 1508/1972 | 1424/1779 | 475/592 | chr2 | 215346862 | ||
chr2:215346937 | G | A | 1 | a0005 | 2 | HG03471.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.1499G>A | p.Gly500Asp | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/16 | 1583/1972 | 1499/1779 | 500/592 | chr2 | 215346937 | ||
chr2:215349546 | C | T | 1 | a0010 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.1670C>T | p.Ala557Val | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 16/16 | 1754/1972 | 1670/1779 | 557/592 | chr2 | 215349546 | ||
chr2:215349591 | T | C | 1 | a0009 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1715T>C | p.Ile572Thr | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 16/16 | 1799/1972 | 1715/1779 | 572/592 | chr2 | 215349591 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:215326009 | T | C | 1 | a0002c0014 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.402T>C | p.Ala134Ala | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/16 | 486/1972 | 402/1779 | 134/592 | chr2 | 215326009 | ||
chr2:215326075 | G | T | 1 | a0002c0016 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.468G>T | p.Thr156Thr | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/16 | 552/1972 | 468/1779 | 156/592 | chr2 | 215326075 | ||
chr2:215326890 | C | T | 1 | a0001c0007 | 2 | HG01891.hp1 HG02723.hp1 |
synonymous_variant | LOW | c.600C>T | p.Gly200Gly | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/16 | 684/1972 | 600/1779 | 200/592 | chr2 | 215326890 | ||
chr2:215346926 | T | C | 1 | a0001c0005 | 3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.1488T>C | p.Thr496Thr | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/16 | 1572/1972 | 1488/1779 | 496/592 | chr2 | 215346926 | ||
chr2:215346932 | C | G | 1 | a0001c0011 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.1494C>G | p.Thr498Thr | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/16 | 1578/1972 | 1494/1779 | 498/592 | chr2 | 215346932 | ||
chr2:215349132 | A | G | 1 | a0001c0010 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.1542A>G | p.Glu514Glu | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 15/16 | 1626/1972 | 1542/1779 | 514/592 | chr2 | 215349132 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:215312068 | C | T | 1 | a0001c0001t0007 | 5 | HG00438.hp2 HG01943.hp1 HG01978.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-75C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/16 | chr2 | 215312068 | ||||||
chr2:215312076 | C | T | 1 | a0001c0001t0009 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-67C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/16 | 67 | chr2 | 215312076 | |||||
chr2:215312082 | C | T | 3 | a0001c0001t0005a0001c0005t0005a0005c0006t0005 | 9 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-61C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/16 | 61 | chr2 | 215312082 | |||||
chr2:215312084 | T | G | 4 | a0001c0001t0003a0002c0002t0003a0002c0016t0003others(1): Show | 59 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-59T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/16 | 59 | chr2 | 215312084 | |||||
chr2:215312101 | C | G | 1 | a0001c0001t0004 | 21 | HG01256.hp1 HG01258.hp1 HG01975.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-42C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/16 | 42 | chr2 | 215312101 | |||||
chr2:215312101 | C | T | 4 | a0001c0001t0002a0001c0001t0007a0001c0011t0002others(1): Show | 82 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(79): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-42C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/16 | chr2 | 215312101 | ||||||
chr2:215312120 | C | T | 2 | a0001c0001t0008a0001c0010t0008 | 2 | HG01256.hp2 HG04115.hp1 |
5_prime_UTR_variant | MODIFIER | c.-23C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/16 | 23 | chr2 | 215312120 | |||||
chr2:215312128 | C | T | 2 | a0001c0001t0006a0011c0017t0006 | 6 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-15C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/16 | 15 | chr2 | 215312128 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:215312237 | C | T | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19+76C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/15 | chr2 | 215312237 | ||||||
chr2:215312238 | G | A | 1 | a0001c0010t0008g0046 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.19+77G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/15 | chr2 | 215312238 | ||||||
chr2:215312240 | G | C | 1 | a0001c0001t0001g0019 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.19+79G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/15 | chr2 | 215312240 | ||||||
chr2:215312255 | G | A | 1 | a0002c0002t0003g0047 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19+94G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/15 | chr2 | 215312255 | ||||||
chr2:215312268 | G | A | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.19+107G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/15 | chr2 | 215312268 | ||||||
chr2:215312278 | C | T | 1 | a0002c0002t0003g0232 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.19+117C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/15 | chr2 | 215312278 | ||||||
chr2:215312341 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20-157G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/15 | chr2 | 215312341 | ||||||
chr2:215312347 | A | G | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0010c0009t0001g0233others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-151A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/15 | chr2 | 215312347 | ||||||
chr2:215312420 | C | T | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.20-78C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 1/15 | chr2 | 215312420 | ||||||
chr2:215312656 | T | A | 11 | a0001c0001t0004g0004a0001c0001t0004g0020a0001c0001t0004g0050others(8): Show | 22 | HG01256.hp1 HG01258.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.146+32T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215312656 | ||||||
chr2:215312725 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.146+101A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215312725 | ||||||
chr2:215312903 | A | G | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.146+279A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215312903 | ||||||
chr2:215312986 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.146+362A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215312986 | ||||||
chr2:215313003 | A | G | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.146+379A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313003 | ||||||
chr2:215313035 | TGTG | T | 43 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0002g0007others(40): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.146+415_146+417del others(3): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 215313035 | |||||
chr2:215313052 | G | A | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.146+428G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313052 | ||||||
chr2:215313150 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.146+526G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313150 | ||||||
chr2:215313205 | C | T | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.146+581C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313205 | ||||||
chr2:215313293 | A | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.146+669A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313293 | ||||||
chr2:215313371 | G | T | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.146+747G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313371 | ||||||
chr2:215313410 | A | G | 1 | a0002c0002t0001g0226 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.146+786A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313410 | ||||||
chr2:215313436 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.146+812A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313436 | ||||||
chr2:215313439 | C | T | 43 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0002g0007others(40): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.146+815C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313439 | ||||||
chr2:215313473 | G | A | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.146+849G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313473 | ||||||
chr2:215313515 | C | A | 1 | a0002c0002t0003g0232 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.146+891C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313515 | ||||||
chr2:215313796 | C | T | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.146+1172C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313796 | ||||||
chr2:215313810 | C | T | 1 | a0001c0001t0005g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.146+1186C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313810 | ||||||
chr2:215313851 | G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.146+1227G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313851 | ||||||
chr2:215313852 | T | C | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.146+1228T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215313852 | ||||||
chr2:215314038 | A | G | 1 | a0002c0002t0001g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.146+1414A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314038 | ||||||
chr2:215314085 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.146+1461C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314085 | ||||||
chr2:215314148 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.146+1524T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314148 | ||||||
chr2:215314163 | T | A | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.146+1539T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314163 | ||||||
chr2:215314198 | C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.146+1574C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314198 | ||||||
chr2:215314375 | T | A | 1 | a0002c0002t0003g0095 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.146+1751T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314375 | ||||||
chr2:215314438 | T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.146+1814T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314438 | ||||||
chr2:215314520 | T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(221): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.146+1896T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314520 | ||||||
chr2:215314527 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.146+1903T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314527 | ||||||
chr2:215314528 | C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0164others(111): Show | 188 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.146+1904C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314528 | ||||||
chr2:215314541 | C | G | 52 | a0001c0001t0003g0198a0002c0002t0001g0011a0002c0002t0001g0173others(49): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.146+1917C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314541 | ||||||
chr2:215314555 | A | G | 2 | a0002c0002t0001g0223a0002c0002t0003g0202 | 2 | HG01168.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.146+1931A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314555 | ||||||
chr2:215314655 | C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.146+2031C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314655 | ||||||
chr2:215314699 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.146+2075C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215314699 | ||||||
chr2:215315077 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.146+2453G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315077 | ||||||
chr2:215315101 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.146+2477C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315101 | ||||||
chr2:215315265 | T | C | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.146+2641T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315265 | ||||||
chr2:215315370 | A | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(211): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.146+2746A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315370 | ||||||
chr2:215315377 | T | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.146+2753T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315377 | ||||||
chr2:215315500 | C | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(216): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.147-2657C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315500 | ||||||
chr2:215315506 | A | G | 1 | a0003c0003t0001g0217 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.147-2651A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315506 | ||||||
chr2:215315588 | A | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.147-2569A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315588 | ||||||
chr2:215315658 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.147-2499G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315658 | ||||||
chr2:215315677 | G | A | 6 | a0001c0001t0005g0024a0001c0001t0005g0098a0001c0001t0005g0224others(3): Show | 9 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-2480G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315677 | ||||||
chr2:215315699 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.147-2458C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315699 | ||||||
chr2:215315752 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.147-2405C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315752 | ||||||
chr2:215315775 | A | G | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147-2382A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315775 | ||||||
chr2:215315811 | C | T | 1 | a0001c0001t0002g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147-2346C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315811 | ||||||
chr2:215315836 | T | A | 56 | a0001c0001t0003g0198a0002c0002t0001g0011a0002c0002t0001g0038others(53): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.147-2321T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315836 | ||||||
chr2:215315932 | A | G | 2 | a0001c0001t0001g0227a0010c0009t0001g0233 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.147-2225A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215315932 | ||||||
chr2:215315954 | CA | C | 7 | a0001c0001t0001g0037a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 8 | HG01515.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.147-2188delA | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 215315954 | |||||
chr2:215316039 | A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0156a0001c0001t0001g0157 | 4 | HG02055.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-2118A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316039 | ||||||
chr2:215316214 | C | T | 1 | a0002c0002t0003g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.147-1943C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316214 | ||||||
chr2:215316216 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.147-1941C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316216 | ||||||
chr2:215316312 | G | A | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.147-1845G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316312 | ||||||
chr2:215316445 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.147-1712G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316445 | ||||||
chr2:215316489 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.147-1668A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316489 | ||||||
chr2:215316509 | G | C | 3 | a0001c0001t0001g0227a0010c0009t0001g0233a0012c0018t0001g0048 | 3 | HG02109.hp1 HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.147-1648G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316509 | ||||||
chr2:215316556 | C | T | 56 | a0001c0001t0003g0198a0002c0002t0001g0011a0002c0002t0001g0038others(53): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.147-1601C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316556 | ||||||
chr2:215316659 | A | G | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.147-1498A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316659 | ||||||
chr2:215316664 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.147-1493A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316664 | ||||||
chr2:215316750 | T | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.147-1407T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316750 | ||||||
chr2:215316826 | A | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.147-1331A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316826 | ||||||
chr2:215316853 | C | T | 1 | a0005c0006t0005g0100 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.147-1304C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316853 | ||||||
chr2:215316856 | G | A | 6 | a0001c0001t0005g0024a0001c0001t0005g0098a0001c0001t0005g0224others(3): Show | 9 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-1301G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316856 | ||||||
chr2:215316872 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.147-1285C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316872 | ||||||
chr2:215316945 | A | G | 1 | a0001c0010t0008g0046 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.147-1212A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215316945 | ||||||
chr2:215317105 | C | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(13): Show | 24 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.147-1052C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317105 | ||||||
chr2:215317145 | C | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(67): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.147-1012C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317145 | ||||||
chr2:215317172 | A | G | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-985A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317172 | ||||||
chr2:215317278 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.147-879G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317278 | ||||||
chr2:215317409 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.147-748C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317409 | ||||||
chr2:215317442 | C | G | 1 | a0001c0001t0002g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.147-715C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317442 | ||||||
chr2:215317549 | G | T | 1 | a0002c0002t0003g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.147-608G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317549 | ||||||
chr2:215317565 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.147-592G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317565 | ||||||
chr2:215317675 | G | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(19): Show | 30 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.147-482G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317675 | ||||||
chr2:215317708 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.147-449C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317708 | ||||||
chr2:215317716 | C | G | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147-441C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317716 | ||||||
chr2:215317877 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.147-280G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317877 | ||||||
chr2:215317910 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.147-247G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317910 | ||||||
chr2:215317926 | A | G | 1 | a0005c0006t0005g0100 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.147-231A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317926 | ||||||
chr2:215317991 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.147-166G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215317991 | ||||||
chr2:215318046 | A | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.147-111A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215318046 | ||||||
chr2:215318047 | C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(71): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.147-110C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 2/15 | chr2 | 215318047 | ||||||
chr2:215318323 | G | T | 1 | a0001c0001t0004g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223+90G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215318323 | ||||||
chr2:215318354 | T | A | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+121T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215318354 | ||||||
chr2:215318384 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.223+151G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215318384 | ||||||
chr2:215318705 | A | G | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+472A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215318705 | ||||||
chr2:215318751 | T | C | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.223+518T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215318751 | ||||||
chr2:215318884 | C | CT | 11 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(8): Show | 23 | HG01256.hp1 HG01258.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.223+663dupT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 215318884 | |||||
chr2:215318884 | C | T | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.223+651C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215318884 | ||||||
chr2:215318984 | A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.224-681A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215318984 | ||||||
chr2:215319070 | G | A | 1 | a0001c0001t0005g0024 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.224-595G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319070 | ||||||
chr2:215319078 | A | C | 1 | a0001c0001t0002g0081 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.224-587A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319078 | ||||||
chr2:215319093 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.224-572C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319093 | ||||||
chr2:215319100 | C | T | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.224-565C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319100 | ||||||
chr2:215319112 | C | G | 1 | a0001c0001t0004g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.224-553C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319112 | ||||||
chr2:215319140 | A | G | 1 | a0009c0008t0001g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.224-525A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319140 | ||||||
chr2:215319192 | T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0120a0001c0001t0001g0160 | 5 | NA18945.hp1 NA19001.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-473T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319192 | ||||||
chr2:215319499 | C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(13): Show | 24 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.224-166C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319499 | ||||||
chr2:215319509 | A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.224-156A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319509 | ||||||
chr2:215319548 | T | A | 2 | a0010c0009t0001g0233a0012c0018t0001g0048 | 2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.224-117T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319548 | ||||||
chr2:215319657 | T | A | 1 | a0001c0001t0004g0053 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.224-8T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 3/15 | chr2 | 215319657 | ||||||
chr2:215319759 | A | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.290+28A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215319759 | ||||||
chr2:215319826 | C | T | 1 | a0002c0002t0003g0197 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.290+95C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215319826 | ||||||
chr2:215319891 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.290+160A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215319891 | ||||||
chr2:215319896 | A | G | 2 | a0005c0006t0005g0099a0005c0006t0005g0100 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.290+165A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215319896 | ||||||
chr2:215319917 | T | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+186T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215319917 | ||||||
chr2:215320026 | T | C | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+295T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320026 | ||||||
chr2:215320191 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.290+460T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320191 | ||||||
chr2:215320310 | T | C | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+579T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320310 | ||||||
chr2:215320314 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.290+583A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320314 | ||||||
chr2:215320382 | C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(216): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.290+651C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320382 | ||||||
chr2:215320525 | G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.290+794G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320525 | ||||||
chr2:215320622 | C | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+891C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320622 | ||||||
chr2:215320624 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.290+893G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320624 | ||||||
chr2:215320875 | C | T | 6 | a0001c0001t0005g0024a0001c0001t0005g0098a0001c0001t0005g0224others(3): Show | 9 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.290+1144C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320875 | ||||||
chr2:215320905 | T | G | 1 | a0001c0001t0004g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290+1174T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320905 | ||||||
chr2:215320948 | A | G | 1 | a0001c0001t0001g0012 | 4 | HG02559.hp2 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+1217A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320948 | ||||||
chr2:215320969 | C | G | 45 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0002g0007others(42): Show | 85 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.290+1238C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320969 | ||||||
chr2:215320972 | C | T | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+1241C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320972 | ||||||
chr2:215320981 | A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(3): Show | 15 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.290+1250A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215320981 | ||||||
chr2:215321059 | C | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+1328C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321059 | ||||||
chr2:215321102 | C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(11): Show | 22 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.290+1371C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321102 | ||||||
chr2:215321122 | C | T | 1 | a0001c0005t0005g0014 | 3 | HG02809.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.290+1391C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321122 | ||||||
chr2:215321239 | G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 5 | HG02280.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+1508G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321239 | ||||||
chr2:215321239 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.290+1508G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321239 | ||||||
chr2:215321306 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.290+1575C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321306 | ||||||
chr2:215321362 | G | GTT | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.290+1632_290+1633d others(4): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 215321362 | |||||
chr2:215321490 | A | G | 1 | a0003c0003t0001g0214 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.290+1759A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321490 | ||||||
chr2:215321513 | T | TG | 3 | a0002c0002t0003g0170a0002c0002t0003g0171a0002c0002t0003g0172 | 3 | HG02738.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.290+1784dupG | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 215321513 | |||||
chr2:215321556 | C | T | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.290+1825C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321556 | ||||||
chr2:215321590 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.290+1859C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321590 | ||||||
chr2:215321673 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.290+1942A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321673 | ||||||
chr2:215321705 | T | C | 3 | a0002c0002t0001g0038a0002c0002t0001g0163a0002c0002t0001g0226 | 4 | HG00099.hp2 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+1974T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321705 | ||||||
chr2:215321918 | T | A | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+2187T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321918 | ||||||
chr2:215321928 | C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.290+2197C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321928 | ||||||
chr2:215321929 | G | A | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+2198G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321929 | ||||||
chr2:215321978 | A | C | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+2247A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215321978 | ||||||
chr2:215322007 | G | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(17): Show | 28 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.290+2276G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322007 | ||||||
chr2:215322082 | TAATAGAG others(10): Show |
T | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+2353_290+2369d others(19): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 215322082 | |||||
chr2:215322137 | G | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+2406G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322137 | ||||||
chr2:215322190 | A | G | 2 | a0002c0002t0003g0045a0002c0002t0003g0190 | 3 | HG01099.hp1 HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.290+2459A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322190 | ||||||
chr2:215322265 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.290+2534G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322265 | ||||||
chr2:215322329 | C | CT | 14 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0147others(11): Show | 19 | HG00642.hp1 HG00673.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.290+2615dupT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 215322329 | |||||
chr2:215322329 | C | CTTT | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+2613_290+2615d others(5): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 215322329 | |||||
chr2:215322333 | T | C | 55 | a0002c0002t0001g0011a0002c0002t0001g0038a0002c0002t0001g0163others(52): Show | 77 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.290+2602T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322333 | ||||||
chr2:215322412 | C | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.290+2681C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322412 | ||||||
chr2:215322432 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.290+2701C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322432 | ||||||
chr2:215322447 | A | G | 4 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0111others(1): Show | 6 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+2716A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322447 | ||||||
chr2:215322533 | T | A | 1 | a0001c0001t0002g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.291-2708T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322533 | ||||||
chr2:215322561 | A | T | 36 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0002g0007others(33): Show | 75 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.291-2680A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322561 | ||||||
chr2:215322583 | C | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(22): Show | 34 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.291-2658C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322583 | ||||||
chr2:215322622 | G | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-2619G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322622 | ||||||
chr2:215322774 | A | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.291-2467A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322774 | ||||||
chr2:215322897 | T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.291-2344T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322897 | ||||||
chr2:215322898 | G | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-2343G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322898 | ||||||
chr2:215322948 | T | A | 1 | a0002c0002t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.291-2293T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322948 | ||||||
chr2:215322968 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.291-2273G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215322968 | ||||||
chr2:215323083 | T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.291-2158T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323083 | ||||||
chr2:215323093 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291-2148C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323093 | ||||||
chr2:215323099 | C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(17): Show | 28 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.291-2142C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323099 | ||||||
chr2:215323147 | G | C | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.291-2094G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323147 | ||||||
chr2:215323148 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.291-2093T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323148 | ||||||
chr2:215323192 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.291-2049G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323192 | ||||||
chr2:215323291 | C | T | 1 | a0002c0002t0003g0189 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.291-1950C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323291 | ||||||
chr2:215323454 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.291-1787T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323454 | ||||||
chr2:215323565 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.291-1676G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323565 | ||||||
chr2:215323635 | T | A | 1 | a0001c0001t0007g0058 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.291-1606T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323635 | ||||||
chr2:215323820 | G | C | 6 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-1421G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323820 | ||||||
chr2:215323835 | G | T | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.291-1406G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323835 | ||||||
chr2:215323884 | T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.291-1357T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323884 | ||||||
chr2:215323923 | T | C | 7 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 8 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-1318T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323923 | ||||||
chr2:215323998 | T | G | 6 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-1243T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215323998 | ||||||
chr2:215324119 | A | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.291-1122A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215324119 | ||||||
chr2:215324177 | A | G | 7 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 8 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-1064A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215324177 | ||||||
chr2:215324341 | C | G | 6 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-900C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215324341 | ||||||
chr2:215324401 | A | G | 6 | a0001c0001t0005g0024a0001c0001t0005g0098a0001c0001t0005g0224others(3): Show | 9 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.291-840A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215324401 | ||||||
chr2:215324679 | T | A | 1 | a0002c0002t0003g0174 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.291-562T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215324679 | ||||||
chr2:215324765 | C | T | 14 | a0001c0001t0001g0203a0001c0001t0001g0213a0003c0003t0001g0205others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.291-476C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215324765 | ||||||
chr2:215324921 | C | A | 1 | a0001c0001t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.291-320C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215324921 | ||||||
chr2:215324933 | C | A | 1 | a0001c0001t0004g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.291-308C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215324933 | ||||||
chr2:215324966 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.291-275G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215324966 | ||||||
chr2:215324997 | G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.291-244G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215324997 | ||||||
chr2:215325001 | T | G | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.291-240T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215325001 | ||||||
chr2:215325065 | C | T | 6 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-176C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215325065 | ||||||
chr2:215325102 | A | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.291-139A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215325102 | ||||||
chr2:215325122 | A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.291-119A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215325122 | ||||||
chr2:215325150 | G | A | 1 | a0002c0002t0001g0191 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.291-91G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215325150 | ||||||
chr2:215325195 | A | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.291-46A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215325195 | ||||||
chr2:215325204 | C | T | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-37C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 4/15 | chr2 | 215325204 | ||||||
chr2:215325618 | A | G | 6 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.379+289A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 5/15 | chr2 | 215325618 | ||||||
chr2:215325714 | C | T | 1 | a0001c0001t0005g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.380-273C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 5/15 | chr2 | 215325714 | ||||||
chr2:215325730 | T | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0228 | 3 | HG01257.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.380-257T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 5/15 | chr2 | 215325730 | ||||||
chr2:215325802 | G | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(17): Show | 28 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.380-185G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 5/15 | chr2 | 215325802 | ||||||
chr2:215325857 | C | A | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380-130C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 5/15 | chr2 | 215325857 | ||||||
chr2:215325931 | C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(88): Show | 150 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.380-56C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 5/15 | chr2 | 215325931 | ||||||
chr2:215325936 | C | T | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380-51C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 5/15 | chr2 | 215325936 | ||||||
chr2:215325968 | A | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.380-19A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 5/15 | chr2 | 215325968 | ||||||
chr2:215325969 | G | A | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380-18G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 5/15 | chr2 | 215325969 | ||||||
chr2:215326333 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.531+195G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326333 | ||||||
chr2:215326343 | G | A | 2 | a0002c0002t0003g0045a0002c0002t0003g0190 | 3 | HG01099.hp1 HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.531+205G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326343 | ||||||
chr2:215326375 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.531+237C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326375 | ||||||
chr2:215326426 | G | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.531+288G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326426 | ||||||
chr2:215326487 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.532-335G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326487 | ||||||
chr2:215326529 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.532-293G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326529 | ||||||
chr2:215326540 | G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(143): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.532-282G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326540 | ||||||
chr2:215326558 | T | C | 7 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 8 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.532-264T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326558 | ||||||
chr2:215326559 | G | A | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.532-263G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326559 | ||||||
chr2:215326609 | C | CA | 11 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(8): Show | 12 | HG00438.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.532-198dupA | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 215326609 | |||||
chr2:215326792 | C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(94): Show | 159 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.532-30C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326792 | ||||||
chr2:215326810 | C | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.532-12C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 6/15 | chr2 | 215326810 | ||||||
chr2:215327029 | G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.688+51G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215327029 | ||||||
chr2:215327081 | G | A | 6 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.688+103G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215327081 | ||||||
chr2:215327413 | G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 8 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.688+435G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215327413 | ||||||
chr2:215327444 | A | G | 6 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.688+466A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215327444 | ||||||
chr2:215327651 | C | T | 3 | a0001c0001t0002g0007a0001c0001t0002g0077a0001c0001t0002g0078 | 6 | NA18941.hp1 NA18953.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.688+673C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215327651 | ||||||
chr2:215327714 | G | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.688+736G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215327714 | ||||||
chr2:215327889 | AT | A | 10 | a0001c0001t0001g0094a0001c0001t0001g0167a0001c0001t0001g0168others(7): Show | 11 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.688+929delT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215327889 | |||||
chr2:215327889 | ATT | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(223): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.688+928_688+929del others(2): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215327889 | |||||
chr2:215327907 | T | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0096others(7): Show | 12 | HG00280.hp1 HG00642.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.688+929T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215327907 | ||||||
chr2:215327921 | G | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.688+943G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215327921 | ||||||
chr2:215328065 | G | A | 15 | a0001c0001t0001g0203a0001c0001t0001g0213a0003c0003t0001g0205others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+1087G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328065 | ||||||
chr2:215328068 | T | C | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.688+1090T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328068 | ||||||
chr2:215328076 | G | A | 36 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0002g0007others(33): Show | 75 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.688+1098G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328076 | ||||||
chr2:215328078 | T | C | 2 | a0002c0002t0003g0095a0002c0002t0003g0175 | 2 | HG02080.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.688+1100T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328078 | ||||||
chr2:215328089 | G | T | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.688+1111G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328089 | ||||||
chr2:215328274 | C | T | 1 | a0002c0002t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.688+1296C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328274 | ||||||
chr2:215328274 | CG | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(71): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.688+1298delG | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215328274 | |||||
chr2:215328276 | G | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(71): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.688+1298G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328276 | ||||||
chr2:215328294 | G | A | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.688+1316G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328294 | ||||||
chr2:215328310 | A | C | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.688+1332A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328310 | ||||||
chr2:215328377 | C | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.688+1399C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328377 | ||||||
chr2:215328414 | A | G | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.688+1436A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328414 | ||||||
chr2:215328581 | C | A | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.688+1603C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328581 | ||||||
chr2:215328606 | C | G | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.688+1628C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328606 | ||||||
chr2:215328606 | C | T | 36 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0002g0007others(33): Show | 75 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.688+1628C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328606 | ||||||
chr2:215328638 | T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.688+1660T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328638 | ||||||
chr2:215328664 | T | C | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.688+1686T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328664 | ||||||
chr2:215328710 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.688+1732G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328710 | ||||||
chr2:215328718 | C | CT | 94 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(91): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.688+1756dupT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215328718 | |||||
chr2:215328781 | G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.688+1803G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328781 | ||||||
chr2:215328791 | C | T | 3 | a0002c0002t0003g0044a0002c0002t0003g0183a0002c0002t0003g0184 | 4 | HG00408.hp2 HG02080.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.688+1813C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328791 | ||||||
chr2:215328848 | G | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.688+1870G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328848 | ||||||
chr2:215328877 | C | T | 53 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0173others(50): Show | 74 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.688+1899C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328877 | ||||||
chr2:215328905 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.688+1927T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328905 | ||||||
chr2:215328941 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.688+1963T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328941 | ||||||
chr2:215328978 | A | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.688+2000A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215328978 | ||||||
chr2:215329054 | T | A | 1 | a0001c0001t0002g0076 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.688+2076T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215329054 | ||||||
chr2:215329278 | T | C | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.688+2300T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215329278 | ||||||
chr2:215329340 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.688+2362T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215329340 | ||||||
chr2:215329703 | T | A | 1 | a0001c0001t0002g0083 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.689-2679T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215329703 | ||||||
chr2:215329735 | T | C | 3 | a0002c0002t0001g0038a0002c0002t0001g0163a0002c0002t0001g0226 | 4 | HG00099.hp2 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.689-2647T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215329735 | ||||||
chr2:215329774 | T | C | 1 | a0008c0012t0001g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.689-2608T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215329774 | ||||||
chr2:215329784 | G | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0121a0001c0001t0001g0144others(4): Show | 9 | HG00558.hp2 HG00621.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.689-2598G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215329784 | ||||||
chr2:215329803 | C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(71): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.689-2579C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215329803 | ||||||
chr2:215329863 | A | G | 56 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(53): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.689-2519A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215329863 | ||||||
chr2:215329911 | AC | A | 56 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(53): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.689-2469delC | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215329911 | |||||
chr2:215329915 | C | T | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.689-2467C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215329915 | ||||||
chr2:215330068 | C | T | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.689-2314C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330068 | ||||||
chr2:215330124 | G | T | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.689-2258G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330124 | ||||||
chr2:215330148 | G | A | 1 | a0008c0012t0001g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.689-2234G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330148 | ||||||
chr2:215330290 | A | C | 4 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0111others(1): Show | 6 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.689-2092A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330290 | ||||||
chr2:215330357 | T | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.689-2025T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330357 | ||||||
chr2:215330398 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.689-1984C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330398 | ||||||
chr2:215330448 | G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(139): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.689-1934G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330448 | ||||||
chr2:215330558 | G | A | 52 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(49): Show | 72 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.689-1824G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330558 | ||||||
chr2:215330614 | T | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.689-1768T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330614 | ||||||
chr2:215330639 | T | C | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.689-1743T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330639 | ||||||
chr2:215330712 | C | CT | 17 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0146others(14): Show | 23 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.689-1656dupT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215330712 | |||||
chr2:215330824 | A | G | 1 | a0001c0001t0003g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.689-1558A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330824 | ||||||
chr2:215330841 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.689-1541G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330841 | ||||||
chr2:215330886 | T | C | 1 | a0002c0002t0001g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.689-1496T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330886 | ||||||
chr2:215330907 | C | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.689-1475C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330907 | ||||||
chr2:215330923 | A | G | 1 | a0002c0002t0003g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.689-1459A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330923 | ||||||
chr2:215330986 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.689-1396G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330986 | ||||||
chr2:215330996 | A | G | 1 | a0001c0001t0002g0078 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.689-1386A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215330996 | ||||||
chr2:215331193 | A | T | 1 | a0001c0001t0002g0078 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.689-1189A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331193 | ||||||
chr2:215331207 | G | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.689-1175G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331207 | ||||||
chr2:215331234 | G | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.689-1148G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331234 | ||||||
chr2:215331240 | A | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(129): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.689-1142A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331240 | ||||||
chr2:215331322 | G | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.689-1060G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331322 | ||||||
chr2:215331379 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.689-1003G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331379 | ||||||
chr2:215331380 | G | GGTT | 5 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0143others(2): Show | 8 | HG00735.hp2 HG02300.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.689-1001_689-999du others(4): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215331380 | |||||
chr2:215331381 | G | GT | 53 | a0001c0001t0001g0131a0001c0001t0001g0213a0001c0001t0001g0219others(50): Show | 73 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.689-983dupT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215331381 | |||||
chr2:215331381 | G | GTT | 11 | a0001c0001t0002g0082a0002c0002t0002g0023a0002c0002t0002g0088others(8): Show | 12 | HG01243.hp2 HG01928.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.689-984_689-983dup others(2): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215331381 | |||||
chr2:215331381 | GT | G | 39 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(36): Show | 47 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.689-983delT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215331381 | |||||
chr2:215331382 | T | TTG | 74 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(71): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.689-999_689-998ins others(2): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215331382 | |||||
chr2:215331421 | T | C | 2 | a0001c0001t0006g0026a0001c0001t0006g0111 | 3 | HG01167.hp1 HG01169.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.689-961T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331421 | ||||||
chr2:215331460 | A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.689-922A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331460 | ||||||
chr2:215331531 | C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(71): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.689-851C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331531 | ||||||
chr2:215331604 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.689-778G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331604 | ||||||
chr2:215331642 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.689-740A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331642 | ||||||
chr2:215331666 | G | A | 1 | a0005c0006t0005g0100 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.689-716G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331666 | ||||||
chr2:215331717 | C | T | 13 | a0001c0001t0001g0039a0001c0001t0001g0164a0001c0001t0001g0165others(10): Show | 25 | HG01256.hp1 HG01258.hp1 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.689-665C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331717 | ||||||
chr2:215331718 | TTTCTGTG others(8): Show |
T | 4 | a0001c0001t0001g0102a0001c0001t0004g0050a0001c0001t0004g0051others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.689-659_689-645del others(15): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215331718 | |||||
chr2:215331778 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.689-604G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331778 | ||||||
chr2:215331887 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.689-495A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331887 | ||||||
chr2:215331963 | G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.689-419G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331963 | ||||||
chr2:215331984 | C | T | 2 | a0001c0001t0001g0227a0012c0018t0001g0048 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.689-398C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215331984 | ||||||
chr2:215332077 | C | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0001g0142 | 4 | NA18953.hp2 NA18961.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.689-305C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215332077 | ||||||
chr2:215332131 | C | CGT | 15 | a0001c0001t0001g0039a0001c0001t0001g0164a0001c0001t0001g0165others(12): Show | 30 | HG01256.hp1 HG01258.hp1 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.689-208_689-207dup others(2): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | C | CGTGT | 15 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(12): Show | 23 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.689-210_689-207dup others(4): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | C | CGTGTGT | 8 | a0001c0001t0001g0103a0001c0001t0001g0113a0001c0001t0001g0162others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.689-212_689-207dup others(6): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | C | CGTGTGTG others(1): Show |
4 | a0003c0003t0001g0205a0003c0003t0001g0206a0003c0003t0001g0215others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.689-214_689-207dup others(8): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | C | CGTGTGTG others(7): Show |
1 | a0003c0003t0001g0214 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.689-220_689-207dup others(14): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | CGT | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0229a0001c0001t0002g0001others(23): Show | 58 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.689-208_689-207del others(2): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | CGTGT | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(3): Show | 16 | HG01069.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.689-210_689-207del others(4): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | CGTGTGT | C | 8 | a0001c0001t0001g0220a0001c0001t0002g0082a0001c0001t0005g0024others(5): Show | 11 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.689-212_689-207del others(6): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | CGTGTGTG others(1): Show |
C | 9 | a0001c0001t0001g0126a0001c0001t0001g0132a0001c0001t0001g0133others(6): Show | 10 | HG01099.hp2 HG01123.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.689-214_689-207del others(8): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | CGTGTGTG others(3): Show |
C | 55 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.689-216_689-207del others(10): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | CGTGTGTG others(5): Show |
C | 29 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0029others(26): Show | 36 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.689-218_689-207del others(12): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | CGTGTGTG others(7): Show |
C | 49 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0173others(46): Show | 70 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.689-220_689-207del others(14): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | CGTGTGTG others(9): Show |
C | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.689-222_689-207del others(16): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332131 | CGTGTGTG others(21): Show |
C | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.689-234_689-207del others(28): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 215332131 | |||||
chr2:215332329 | A | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.689-53A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215332329 | ||||||
chr2:215332338 | T | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.689-44T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215332338 | ||||||
chr2:215332366 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.689-16A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 7/15 | chr2 | 215332366 | ||||||
chr2:215332556 | C | G | 1 | a0001c0001t0002g0071 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.814+49C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215332556 | ||||||
chr2:215332697 | G | C | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.814+190G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215332697 | ||||||
chr2:215332777 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.814+270A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215332777 | ||||||
chr2:215332979 | G | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(24): Show | 36 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.815-371G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215332979 | ||||||
chr2:215333056 | G | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.815-294G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215333056 | ||||||
chr2:215333074 | G | A | 36 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0002g0007others(33): Show | 75 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.815-276G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215333074 | ||||||
chr2:215333087 | C | T | 1 | a0008c0012t0001g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.815-263C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215333087 | ||||||
chr2:215333153 | G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.815-197G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215333153 | ||||||
chr2:215333221 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.815-129G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215333221 | ||||||
chr2:215333239 | A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0123 | 3 | HG01109.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.815-111A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215333239 | ||||||
chr2:215333243 | G | GA | 5 | a0001c0001t0002g0082a0001c0001t0005g0024a0001c0001t0005g0098others(2): Show | 8 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.815-103dupA | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 215333243 | |||||
chr2:215333248 | T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.815-102T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215333248 | ||||||
chr2:215333256 | G | A | 16 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0096others(13): Show | 20 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.815-94G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215333256 | ||||||
chr2:215333326 | A | G | 27 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(24): Show | 36 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.815-24A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 8/15 | chr2 | 215333326 | ||||||
chr2:215333503 | A | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.922+46A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215333503 | ||||||
chr2:215333651 | C | T | 36 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0002g0007others(33): Show | 75 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.922+194C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215333651 | ||||||
chr2:215333702 | A | G | 12 | a0003c0003t0001g0205a0003c0003t0001g0206a0003c0003t0001g0211others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.922+245A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215333702 | ||||||
chr2:215333772 | A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.922+315A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215333772 | ||||||
chr2:215333814 | G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.922+357G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215333814 | ||||||
chr2:215333906 | G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.922+449G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215333906 | ||||||
chr2:215333915 | A | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(119): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.922+458A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215333915 | ||||||
chr2:215333973 | T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.922+516T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215333973 | ||||||
chr2:215334041 | C | CAA | 77 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.922+595_922+596dup others(2): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 215334041 | |||||
chr2:215334086 | AAC | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.922+633_922+634del others(2): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 215334086 | |||||
chr2:215334127 | G | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.922+670G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334127 | ||||||
chr2:215334130 | A | G | 1 | a0002c0002t0003g0044 | 2 | HG00408.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.922+673A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334130 | ||||||
chr2:215334189 | C | CT | 19 | a0001c0001t0001g0106a0001c0001t0001g0123a0001c0001t0001g0165others(16): Show | 19 | HG00280.hp2 HG01243.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.923-708dupT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 215334189 | |||||
chr2:215334189 | C | CTT | 33 | a0001c0001t0001g0131a0002c0002t0002g0023a0002c0002t0002g0089others(30): Show | 52 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.923-709_923-708dup others(2): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 215334189 | |||||
chr2:215334189 | C | CTTT | 16 | a0002c0002t0001g0011a0002c0002t0001g0191a0002c0002t0001g0192others(13): Show | 17 | HG01167.hp2 HG01243.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.923-710_923-708dup others(3): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 215334189 | |||||
chr2:215334189 | CTTTTT | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(68): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.923-712_923-708del others(5): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 215334189 | |||||
chr2:215334189 | CTTTTTT | C | 6 | a0001c0001t0001g0132a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 7 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.923-713_923-708del others(6): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 215334189 | |||||
chr2:215334234 | C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.923-685C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334234 | ||||||
chr2:215334340 | C | T | 1 | a0002c0002t0003g0183 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.923-579C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334340 | ||||||
chr2:215334489 | C | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.923-430C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334489 | ||||||
chr2:215334526 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.923-393A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334526 | ||||||
chr2:215334568 | C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.923-351C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334568 | ||||||
chr2:215334575 | G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.923-344G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334575 | ||||||
chr2:215334601 | A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.923-318A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334601 | ||||||
chr2:215334802 | T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.923-117T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334802 | ||||||
chr2:215334825 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.923-94G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334825 | ||||||
chr2:215334828 | T | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(81): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.923-91T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 9/15 | chr2 | 215334828 | ||||||
chr2:215335077 | C | T | 1 | a0001c0001t0004g0020 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1008+73C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 10/15 | chr2 | 215335077 | ||||||
chr2:215335158 | T | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1008+154T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 10/15 | chr2 | 215335158 | ||||||
chr2:215335280 | C | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1008+276C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 10/15 | chr2 | 215335280 | ||||||
chr2:215335431 | G | T | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1008+427G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 10/15 | chr2 | 215335431 | ||||||
chr2:215335563 | C | G | 1 | a0003c0003t0001g0206 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1009-472C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 10/15 | chr2 | 215335563 | ||||||
chr2:215335671 | C | T | 4 | a0001c0001t0005g0024a0001c0001t0005g0098a0001c0001t0005g0224others(1): Show | 7 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009-364C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 10/15 | chr2 | 215335671 | ||||||
chr2:215335952 | A | G | 1 | a0001c0001t0004g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1009-83A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 10/15 | chr2 | 215335952 | ||||||
chr2:215336184 | C | G | 131 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1098+60C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215336184 | ||||||
chr2:215336315 | A | G | 5 | a0001c0001t0007g0058a0001c0001t0007g0061a0001c0001t0007g0068others(2): Show | 5 | HG00438.hp2 HG01943.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+191A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215336315 | ||||||
chr2:215336344 | C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1098+220C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215336344 | ||||||
chr2:215336492 | C | G | 1 | a0001c0001t0002g0081 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1098+368C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215336492 | ||||||
chr2:215336598 | G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(234): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1098+474G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215336598 | ||||||
chr2:215336886 | G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0165 | 3 | HG02630.hp1 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1098+762G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215336886 | ||||||
chr2:215337032 | A | G | 2 | a0001c0001t0004g0051a0001c0001t0004g0052 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1098+908A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215337032 | ||||||
chr2:215337084 | CT | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(233): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1098+975delT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 215337084 | |||||
chr2:215337093 | T | A | 1 | a0002c0002t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1098+969T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215337093 | ||||||
chr2:215337265 | G | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1098+1141G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215337265 | ||||||
chr2:215337334 | C | G | 1 | a0002c0002t0003g0180 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1098+1210C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215337334 | ||||||
chr2:215337431 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1098+1307A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215337431 | ||||||
chr2:215337616 | CTCGGCCT others(16): Show |
C | 1 | a0001c0001t0002g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1099-1161_1099-113 others(27): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 215337616 | |||||
chr2:215337685 | T | G | 7 | a0001c0001t0002g0082a0001c0001t0005g0024a0001c0001t0005g0098others(4): Show | 10 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-1094T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215337685 | ||||||
chr2:215337689 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1099-1090T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215337689 | ||||||
chr2:215337692 | T | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(178): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1099-1087T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215337692 | ||||||
chr2:215337826 | G | A | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-953G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215337826 | ||||||
chr2:215338243 | A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1099-536A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215338243 | ||||||
chr2:215338304 | A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1099-475A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215338304 | ||||||
chr2:215338312 | G | A | 3 | a0002c0002t0001g0038a0002c0002t0001g0163a0002c0002t0001g0226 | 4 | HG00099.hp2 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-467G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215338312 | ||||||
chr2:215338487 | A | G | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-292A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215338487 | ||||||
chr2:215338573 | A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1099-206A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215338573 | ||||||
chr2:215338703 | C | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1099-76C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215338703 | ||||||
chr2:215338711 | T | C | 1 | a0001c0001t0006g0026 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1099-68T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 11/15 | chr2 | 215338711 | ||||||
chr2:215338949 | T | C | 2 | a0002c0002t0003g0045a0002c0002t0003g0190 | 3 | HG01099.hp1 HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1227+42T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215338949 | ||||||
chr2:215339121 | G | A | 1 | a0002c0002t0003g0047 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1227+214G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339121 | ||||||
chr2:215339153 | CA | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1227+247delA | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339153 | ||||||
chr2:215339171 | A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(234): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1227+264A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339171 | ||||||
chr2:215339350 | C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 97 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1227+443C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339350 | ||||||
chr2:215339436 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1227+529A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339436 | ||||||
chr2:215339487 | C | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1227+580C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339487 | ||||||
chr2:215339562 | G | A | 1 | a0001c0001t0004g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1227+655G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339562 | ||||||
chr2:215339637 | T | G | 8 | a0001c0001t0001g0213a0001c0001t0004g0004a0001c0001t0004g0020others(5): Show | 19 | HG01256.hp1 HG01258.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.1227+730T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339637 | ||||||
chr2:215339665 | T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1227+758T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339665 | ||||||
chr2:215339666 | G | A | 13 | a0003c0003t0001g0205a0003c0003t0001g0206a0003c0003t0001g0211others(10): Show | 13 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1227+759G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339666 | ||||||
chr2:215339677 | C | A | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1227+770C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339677 | ||||||
chr2:215339704 | G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0153 | 2 | NA18951.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1227+797G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339704 | ||||||
chr2:215339714 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1227+807A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339714 | ||||||
chr2:215339932 | A | G | 9 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1227+1025A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339932 | ||||||
chr2:215339957 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1227+1050C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339957 | ||||||
chr2:215339976 | C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1227+1069C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339976 | ||||||
chr2:215339998 | A | G | 1 | a0003c0003t0001g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+1091A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215339998 | ||||||
chr2:215340135 | T | C | 1 | a0002c0002t0003g0197 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1227+1228T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340135 | ||||||
chr2:215340265 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1227+1358A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340265 | ||||||
chr2:215340313 | T | C | 1 | a0001c0001t0002g0083 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1227+1406T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340313 | ||||||
chr2:215340416 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1227+1509G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340416 | ||||||
chr2:215340444 | G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(61): Show | 107 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1227+1537G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340444 | ||||||
chr2:215340542 | C | T | 3 | a0002c0002t0001g0038a0002c0002t0001g0163a0002c0002t0001g0226 | 4 | HG00099.hp2 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+1635C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340542 | ||||||
chr2:215340544 | A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(54): Show | 104 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1227+1637A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340544 | ||||||
chr2:215340566 | T | C | 1 | a0002c0002t0003g0202 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1227+1659T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340566 | ||||||
chr2:215340749 | G | C | 55 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(52): Show | 77 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1227+1842G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340749 | ||||||
chr2:215340761 | C | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0031others(15): Show | 23 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1227+1854C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340761 | ||||||
chr2:215340796 | A | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+1889A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340796 | ||||||
chr2:215340911 | T | A | 1 | a0005c0006t0005g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1227+2004T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340911 | ||||||
chr2:215340946 | C | G | 1 | a0002c0002t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1227+2039C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215340946 | ||||||
chr2:215341120 | A | C | 1 | a0001c0001t0002g0067 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1227+2213A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215341120 | ||||||
chr2:215341225 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1227+2318A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215341225 | ||||||
chr2:215341330 | A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1227+2423A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215341330 | ||||||
chr2:215341359 | CTAAGGTT others(2): Show |
C | 2 | a0001c0001t0001g0033a0001c0001t0001g0139 | 3 | NA18942.hp1 NA18948.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1227+2455_1227+246 others(13): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 215341359 | |||||
chr2:215341368 | G | A | 5 | a0001c0001t0001g0131a0002c0002t0003g0041a0002c0002t0003g0043others(2): Show | 7 | HG00544.hp1 HG00544.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227+2461G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215341368 | ||||||
chr2:215341388 | T | C | 3 | a0002c0002t0001g0038a0002c0002t0001g0163a0002c0002t0001g0226 | 4 | HG00099.hp2 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+2481T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215341388 | ||||||
chr2:215341464 | T | C | 1 | a0002c0002t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1227+2557T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215341464 | ||||||
chr2:215341628 | T | A | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1227+2721T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215341628 | ||||||
chr2:215341872 | T | G | 1 | a0001c0001t0004g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1228-2907T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215341872 | ||||||
chr2:215342017 | TC | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1228-2761delC | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342017 | ||||||
chr2:215342019 | A | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1228-2760A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342019 | ||||||
chr2:215342056 | A | G | 56 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(53): Show | 78 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1228-2723A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342056 | ||||||
chr2:215342100 | T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(235): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.1228-2679T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342100 | ||||||
chr2:215342101 | G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0134others(4): Show | 9 | HG00558.hp1 HG02273.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1228-2678G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342101 | ||||||
chr2:215342133 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1228-2646G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342133 | ||||||
chr2:215342161 | A | C | 1 | a0001c0001t0001g0153 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1228-2618A>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342161 | ||||||
chr2:215342239 | G | A | 8 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0002g0082others(5): Show | 11 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228-2540G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342239 | ||||||
chr2:215342240 | A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1228-2539A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342240 | ||||||
chr2:215342241 | G | C | 1 | a0002c0002t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1228-2538G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342241 | ||||||
chr2:215342305 | A | G | 4 | a0001c0001t0001g0102a0001c0001t0004g0050a0001c0001t0004g0051others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-2474A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342305 | ||||||
chr2:215342332 | A | T | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1228-2447A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342332 | ||||||
chr2:215342343 | CT | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(116): Show | 165 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1228-2429delT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 215342343 | |||||
chr2:215342398 | G | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(54): Show | 79 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.1228-2381G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342398 | ||||||
chr2:215342488 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1228-2291C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342488 | ||||||
chr2:215342501 | T | G | 1 | a0001c0001t0002g0064 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1228-2278T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342501 | ||||||
chr2:215342502 | G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(154): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1228-2277G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342502 | ||||||
chr2:215342531 | T | A | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1228-2248T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342531 | ||||||
chr2:215342548 | C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(211): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1228-2231C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342548 | ||||||
chr2:215342553 | G | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(211): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1228-2226G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342553 | ||||||
chr2:215342557 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1228-2222G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342557 | ||||||
chr2:215342570 | T | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0129 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.1228-2209T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342570 | ||||||
chr2:215342667 | T | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1228-2112T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342667 | ||||||
chr2:215342718 | T | C | 1 | a0009c0008t0001g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1228-2061T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342718 | ||||||
chr2:215342736 | A | G | 7 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0002g0082others(4): Show | 10 | HG02145.hp1 HG02280.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1228-2043A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342736 | ||||||
chr2:215342765 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1228-2014C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342765 | ||||||
chr2:215342783 | G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(11): Show | 22 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1228-1996G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342783 | ||||||
chr2:215342806 | G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(153): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1228-1973G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342806 | ||||||
chr2:215342808 | G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 5 | HG02280.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-1971G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342808 | ||||||
chr2:215342844 | T | A | 1 | a0002c0002t0001g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1228-1935T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342844 | ||||||
chr2:215342852 | G | A | 1 | a0009c0008t0001g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1228-1927G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342852 | ||||||
chr2:215342928 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1228-1851C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215342928 | ||||||
chr2:215343024 | G | A | 15 | a0001c0001t0001g0029a0001c0001t0001g0102a0001c0001t0001g0123others(12): Show | 27 | HG01109.hp1 HG01256.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1228-1755G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343024 | ||||||
chr2:215343152 | G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(145): Show | 251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1228-1627G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343152 | ||||||
chr2:215343156 | CT | C | 17 | a0001c0001t0001g0094a0001c0001t0001g0121a0001c0001t0001g0128others(14): Show | 18 | HG00099.hp1 HG00558.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.1228-1608delT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 215343156 | |||||
chr2:215343201 | C | G | 53 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0173others(50): Show | 74 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1228-1578C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343201 | ||||||
chr2:215343206 | T | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-1573T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343206 | ||||||
chr2:215343325 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1228-1454G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343325 | ||||||
chr2:215343335 | G | A | 1 | a0009c0008t0001g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1228-1444G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343335 | ||||||
chr2:215343426 | A | T | 60 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(57): Show | 82 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1228-1353A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343426 | ||||||
chr2:215343512 | T | G | 51 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0191others(48): Show | 72 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1228-1267T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343512 | ||||||
chr2:215343553 | C | A | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1228-1226C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343553 | ||||||
chr2:215343639 | T | TA | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1228-1139dupA | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 215343639 | |||||
chr2:215343693 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1228-1086G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343693 | ||||||
chr2:215343701 | T | A | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1228-1078T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343701 | ||||||
chr2:215343722 | G | A | 5 | a0001c0001t0002g0082a0001c0001t0005g0024a0001c0001t0005g0098others(2): Show | 8 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228-1057G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343722 | ||||||
chr2:215343753 | A | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | NA18981.hp2 NA19007.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1228-1026A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343753 | ||||||
chr2:215343903 | T | C | 1 | a0001c0001t0004g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1228-876T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343903 | ||||||
chr2:215343928 | T | G | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1228-851T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215343928 | ||||||
chr2:215344044 | T | G | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1228-735T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344044 | ||||||
chr2:215344052 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1228-727A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344052 | ||||||
chr2:215344056 | C | T | 1 | a0012c0018t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1228-723C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344056 | ||||||
chr2:215344069 | C | T | 52 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(49): Show | 73 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.1228-710C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344069 | ||||||
chr2:215344070 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1228-709T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344070 | ||||||
chr2:215344115 | G | A | 2 | a0005c0006t0005g0099a0005c0006t0005g0100 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1228-664G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344115 | ||||||
chr2:215344145 | A | T | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1228-634A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344145 | ||||||
chr2:215344227 | A | G | 58 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(55): Show | 80 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1228-552A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344227 | ||||||
chr2:215344310 | A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0096others(1): Show | 6 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228-469A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344310 | ||||||
chr2:215344344 | T | C | 1 | a0002c0002t0003g0175 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1228-435T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344344 | ||||||
chr2:215344544 | A | T | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1228-235A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344544 | ||||||
chr2:215344580 | T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1228-199T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344580 | ||||||
chr2:215344623 | C | T | 2 | a0002c0002t0003g0095a0002c0002t0003g0175 | 2 | HG02080.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1228-156C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344623 | ||||||
chr2:215344635 | G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1228-144G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344635 | ||||||
chr2:215344656 | C | A | 4 | a0004c0004t0001g0204a0004c0004t0001g0207a0004c0004t0001g0208others(1): Show | 4 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-123C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344656 | ||||||
chr2:215344749 | A | G | 57 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(54): Show | 79 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1228-30A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 12/15 | chr2 | 215344749 | ||||||
chr2:215344913 | T | G | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1320+42T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215344913 | ||||||
chr2:215344988 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1320+117C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215344988 | ||||||
chr2:215345039 | A | T | 12 | a0003c0003t0001g0205a0003c0003t0001g0206a0003c0003t0001g0211others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1320+168A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345039 | ||||||
chr2:215345203 | G | T | 1 | a0002c0002t0003g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1320+332G>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345203 | ||||||
chr2:215345215 | G | A | 2 | a0003c0003t0001g0211a0003c0003t0001g0214 | 2 | HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1320+344G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345215 | ||||||
chr2:215345228 | A | G | 58 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(55): Show | 80 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1320+357A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345228 | ||||||
chr2:215345252 | C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0219others(2): Show | 14 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1320+381C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345252 | ||||||
chr2:215345270 | T | C | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1320+399T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345270 | ||||||
chr2:215345437 | C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0025others(11): Show | 22 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1320+566C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345437 | ||||||
chr2:215345513 | C | T | 36 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0002g0007others(33): Show | 75 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1320+642C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345513 | ||||||
chr2:215345576 | C | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1320+705C>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345576 | ||||||
chr2:215345663 | G | C | 1 | a0001c0001t0001g0107 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1320+792G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345663 | ||||||
chr2:215345723 | C | T | 1 | a0002c0002t0003g0171 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1320+852C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345723 | ||||||
chr2:215345805 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1320+934A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345805 | ||||||
chr2:215345892 | C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 5 | HG02280.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1321-867C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345892 | ||||||
chr2:215345909 | A | G | 1 | a0002c0002t0003g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1321-850A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215345909 | ||||||
chr2:215346031 | T | A | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1321-728T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215346031 | ||||||
chr2:215346150 | T | TTTTA | 57 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(54): Show | 79 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1321-589_1321-586d others(6): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 215346150 | |||||
chr2:215346161 | T | A | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1321-598T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215346161 | ||||||
chr2:215346243 | C | G | 1 | a0001c0001t0003g0198 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1321-516C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215346243 | ||||||
chr2:215346342 | T | C | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1321-417T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215346342 | ||||||
chr2:215346455 | C | G | 2 | a0005c0006t0005g0099a0005c0006t0005g0100 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1321-304C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215346455 | ||||||
chr2:215346478 | CT | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(25): Show | 42 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1321-267delT | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 215346478 | |||||
chr2:215346687 | G | A | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 5 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-72G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 13/15 | chr2 | 215346687 | ||||||
chr2:215346959 | G | C | 1 | a0006c0015t0003g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1503+18G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215346959 | ||||||
chr2:215346969 | C | G | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1503+28C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215346969 | ||||||
chr2:215346979 | A | T | 1 | a0004c0004t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1503+38A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215346979 | ||||||
chr2:215346989 | A | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1503+48A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215346989 | ||||||
chr2:215347074 | T | C | 1 | a0003c0003t0001g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1503+133T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347074 | ||||||
chr2:215347100 | A | T | 8 | a0001c0001t0001g0213a0001c0001t0004g0004a0001c0001t0004g0020others(5): Show | 19 | HG01256.hp1 HG01258.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.1503+159A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347100 | ||||||
chr2:215347148 | T | C | 12 | a0003c0003t0001g0205a0003c0003t0001g0206a0003c0003t0001g0211others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1503+207T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347148 | ||||||
chr2:215347366 | C | T | 58 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(55): Show | 80 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1503+425C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347366 | ||||||
chr2:215347369 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1503+428C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347369 | ||||||
chr2:215347519 | T | C | 1 | a0001c0001t0004g0055 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1503+578T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347519 | ||||||
chr2:215347522 | C | T | 1 | a0002c0002t0003g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1503+581C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347522 | ||||||
chr2:215347541 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1503+600G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347541 | ||||||
chr2:215347556 | G | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1503+615G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347556 | ||||||
chr2:215347570 | A | G | 2 | a0005c0006t0005g0099a0005c0006t0005g0100 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1503+629A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347570 | ||||||
chr2:215347616 | T | C | 58 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(55): Show | 80 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1503+675T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347616 | ||||||
chr2:215347751 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1503+810A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347751 | ||||||
chr2:215347771 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1503+830G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347771 | ||||||
chr2:215347891 | T | C | 36 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0002g0007others(33): Show | 75 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1503+950T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347891 | ||||||
chr2:215347905 | T | G | 1 | a0001c0001t0004g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1503+964T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347905 | ||||||
chr2:215347927 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1503+986C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215347927 | ||||||
chr2:215348153 | T | G | 2 | a0002c0002t0003g0010a0002c0002t0003g0177 | 5 | HG01943.hp2 HG02293.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1504-941T>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348153 | ||||||
chr2:215348157 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1504-937T>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348157 | ||||||
chr2:215348403 | C | T | 1 | a0009c0008t0001g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1504-691C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348403 | ||||||
chr2:215348419 | A | G | 2 | a0004c0004t0001g0204a0004c0004t0001g0209 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1504-675A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348419 | ||||||
chr2:215348599 | A | G | 7 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0002g0082others(4): Show | 10 | HG02145.hp1 HG02280.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1504-495A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348599 | ||||||
chr2:215348684 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1504-410C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348684 | ||||||
chr2:215348691 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1504-403G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348691 | ||||||
chr2:215348705 | A | G | 2 | a0005c0006t0005g0099a0005c0006t0005g0100 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1504-389A>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348705 | ||||||
chr2:215348768 | C | T | 1 | a0002c0002t0001g0163 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1504-326C>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348768 | ||||||
chr2:215348927 | CAGCCTGG others(4): Show |
C | 1 | a0009c0008t0001g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1504-164_1504-154d others(13): Show |
ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 215348927 | |||||
chr2:215348963 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1504-131A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348963 | ||||||
chr2:215348966 | A | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(85): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1504-128A>T | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348966 | ||||||
chr2:215348969 | T | A | 13 | a0001c0001t0001g0039a0001c0001t0001g0105a0001c0001t0001g0119others(10): Show | 18 | HG00280.hp1 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1504-125T>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215348969 | ||||||
chr2:215349053 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1504-41G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 14/15 | chr2 | 215349053 | ||||||
chr2:215349306 | C | G | 1 | a0010c0009t0001g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1659+57C>G | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 15/15 | chr2 | 215349306 | ||||||
chr2:215349352 | G | C | 1 | a0002c0002t0003g0042 | 2 | HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1659+103G>C | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 15/15 | chr2 | 215349352 | ||||||
chr2:215349401 | G | A | 56 | a0001c0001t0001g0131a0002c0002t0001g0011a0002c0002t0001g0038others(53): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1660-135G>A | ATIC | ENSG00000138363.15 | transcript | ENST00000236959.14 | protein_coding | 15/15 | chr2 | 215349401 |