geneid | 6948 |
---|---|
ensemblid | ENSG00000185339.10 |
hgncid | 11653 |
symbol | TCN2 |
name | transcobalamin 2 |
refseq_nuc | NM_000355.4 |
refseq_prot | NP_000346.2 |
ensembl_nuc | ENST00000215838.8 |
ensembl_prot | ENSP00000215838.3 |
mane_status | MANE Select |
chr | chr22 |
start | 30607174 |
end | 30627271 |
strand | + |
ver | v1.2 |
region | chr22:30607174-30627271 |
region5000 | chr22:30602174-30632271 |
regionname0 | TCN2_chr22_30607174_30627271 |
regionname5000 | TCN2_chr22_30602174_30632271 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 427 | 175 | 26 | 30 | 105 | 3 | 11 | 81 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002 | 1/1 | 427 | 161 | 2 | 27 | 97 | 6 | 27 | 76 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0003 | 0/0 | 427 | 33 | 12 | 13 | 0 | 5 | 3 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0004 | 0/0 | 427 | 26 | 23 | 2 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0005 | 0/0 | 427 | 22 | 16 | 5 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0006 | 0/0 | 427 | 10 | 5 | 2 | 1 | 0 | 2 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0007 | 0/0 | 427 | 9 | 7 | 1 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0008 | 0/0 | 427 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0009 | 0/0 | 427 | 5 | 0 | 3 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0010 | 0/0 | 427 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0011 | 0/0 | 427 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0012 | 0/0 | 427 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0013 | 0/0 | 427 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0014 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0015 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0016 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0017 | 0/0 | 427 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0018 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0019 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0020 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1284 | 173 | 24 | 30 | 105 | 3 | 11 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0002 | 1/1 | 1284 | 155 | 1 | 22 | 97 | 6 | 27 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0003 | 0/0 | 1284 | 32 | 12 | 13 | 0 | 5 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0004 | 0/0 | 1284 | 26 | 23 | 2 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0005 | 0/0 | 1284 | 18 | 12 | 5 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0006 | 0/0 | 1284 | 10 | 5 | 2 | 1 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0007 | 0/0 | 1284 | 9 | 7 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0008 | 0/0 | 1284 | 8 | 0 | 0 | 8 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0009 | 0/0 | 1284 | 5 | 0 | 3 | 0 | 2 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0010 | 0/0 | 1284 | 5 | 0 | 5 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0011 | 0/0 | 1284 | 4 | 4 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0012 | 0/0 | 1284 | 4 | 4 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0013 | 0/0 | 1284 | 2 | 0 | 1 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0014 | 0/0 | 1284 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0015 | 0/0 | 1284 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0016 | 0/0 | 1284 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0017 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0018 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0019 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0020 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0021 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0022 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0023 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0024 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
c0025 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 909 | 204 | 26 | 28 | 109 | 7 | 32 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0002 | 0/0 | 909 | 89 | 10 | 12 | 65 | 1 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0003 | 0/0 | 909 | 68 | 6 | 12 | 40 | 2 | 8 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0004 | 0/0 | 910 | 31 | 13 | 13 | 0 | 5 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0005 | 0/0 | 909 | 22 | 20 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0006 | 0/0 | 909 | 13 | 3 | 9 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0007 | 0/0 | 910 | 10 | 6 | 1 | 0 | 0 | 3 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0008 | 0/0 | 909 | 5 | 5 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0009 | 0/0 | 909 | 4 | 0 | 4 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0010 | 0/0 | 909 | 3 | 3 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0011 | 0/0 | 909 | 3 | 1 | 1 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0012 | 0/0 | 909 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0013 | 0/0 | 909 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0014 | 0/0 | 909 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0015 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0016 | 0/0 | 909 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0017 | 0/0 | 910 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0018 | 0/0 | 910 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0019 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0020 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0021 | 0/0 | 910 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0022 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0023 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
t0024 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0006 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0013 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0015 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0018 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0052 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0061 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0310 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1284 | 173 | 24 | 30 | 105 | 3 | 11 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0014 | 0/0 | 1284 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0002 | 1/1 | 1284 | 155 | 1 | 22 | 97 | 6 | 27 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0010 | 0/0 | 1284 | 5 | 0 | 5 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0021 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0003c0003 | 0/0 | 1284 | 32 | 12 | 13 | 0 | 5 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0003c0025 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0004c0004 | 0/0 | 1284 | 26 | 23 | 2 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0005c0005 | 0/0 | 1284 | 18 | 12 | 5 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0005c0011 | 0/0 | 1284 | 4 | 4 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0006c0006 | 0/0 | 1284 | 10 | 5 | 2 | 1 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0007c0007 | 0/0 | 1284 | 9 | 7 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0008c0008 | 0/0 | 1284 | 8 | 0 | 0 | 8 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0009c0009 | 0/0 | 1284 | 5 | 0 | 3 | 0 | 2 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0010c0012 | 0/0 | 1284 | 4 | 4 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0011c0016 | 0/0 | 1284 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0012c0015 | 0/0 | 1284 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0013c0013 | 0/0 | 1284 | 2 | 0 | 1 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0014c0020 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0015c0022 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0016c0023 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0017c0024 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0018c0018 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0019c0019 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0020c0017 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2192 | 4 | 2 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0001t0002 | 0/0 | 2192 | 81 | 6 | 10 | 63 | 1 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0001t0003 | 0/0 | 2192 | 64 | 6 | 9 | 40 | 1 | 8 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0001t0006 | 0/0 | 2192 | 13 | 3 | 9 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0001t0008 | 0/0 | 2192 | 5 | 5 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0001t0010 | 0/0 | 2192 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0001t0018 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0001t0021 | 0/0 | 2193 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0001t0023 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0001t0024 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0001c0014t0001 | 0/0 | 2192 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0002t0001 | 1/1 | 2192 | 147 | 1 | 17 | 95 | 6 | 26 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0002t0009 | 0/0 | 2192 | 4 | 0 | 4 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0002t0013 | 0/0 | 2192 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0002t0014 | 0/0 | 2192 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0002t0017 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0002t0019 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0010t0001 | 0/0 | 2192 | 5 | 0 | 5 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0002c0021t0001 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0003c0003t0004 | 0/0 | 2193 | 30 | 12 | 13 | 0 | 5 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0003c0003t0007 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0003c0003t0012 | 0/0 | 2192 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0003c0025t0012 | 0/0 | 2192 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0004c0004t0001 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0004c0004t0002 | 0/0 | 2192 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0004c0004t0005 | 0/0 | 2192 | 22 | 20 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0004c0004t0007 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0005c0005t0001 | 0/0 | 2192 | 12 | 8 | 3 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0005c0005t0002 | 0/0 | 2192 | 4 | 2 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0005c0005t0011 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0005c0005t0015 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0005c0011t0001 | 0/0 | 2192 | 4 | 4 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0006c0006t0001 | 0/0 | 2192 | 9 | 4 | 2 | 1 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0006c0006t0010 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0007c0007t0004 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0007c0007t0007 | 0/0 | 2193 | 8 | 6 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0008c0008t0001 | 0/0 | 2192 | 8 | 0 | 0 | 8 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0009c0009t0003 | 0/0 | 2192 | 4 | 0 | 3 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0009c0009t0016 | 0/0 | 2192 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0010c0012t0001 | 0/0 | 2192 | 3 | 3 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0010c0012t0020 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0011c0016t0001 | 0/0 | 2192 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0012c0015t0001 | 0/0 | 2192 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0013c0013t0011 | 0/0 | 2192 | 2 | 0 | 1 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0014c0020t0001 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0015c0022t0001 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0016c0023t0001 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0017c0024t0001 | 0/0 | 2192 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0018c0018t0002 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0019c0019t0002 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
a0020c0017t0022 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | copy fasta | chr22 | 30602174 | 30632271 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0006 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0006g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0006g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0006g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0008g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0008g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0008g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0008g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0018g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0021g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0023g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0001t0024g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0014t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0001c0014t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0018 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0310 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0009g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0009g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0013g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0014g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0017g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0002t0019g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0010t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0010t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0002c0021t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0007g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0003t0012g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0003c0025t0012g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0001 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0004c0004t0007g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0011g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0005t0015g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0011t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0011t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0005c0011t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0006c0006t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0006c0006t0001g0061 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0006c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0006c0006t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0006c0006t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0006c0006t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0006c0006t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0006c0006t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0007c0007t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0007c0007t0007g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0007c0007t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0007c0007t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0007c0007t0007g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0007c0007t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0008c0008t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0008c0008t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0008c0008t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0008c0008t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0008c0008t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0008c0008t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0009c0009t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0009c0009t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0009c0009t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0009c0009t0016g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0010c0012t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0010c0012t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0010c0012t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0010c0012t0020g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0011c0016t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0011c0016t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0012c0015t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0012c0015t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0013c0013t0011g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0013c0013t0011g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0014c0020t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0015c0022t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0016c0023t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0017c0024t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0018c0018t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0019c0019t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
a0020c0017t0022g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0052 | EUR | GBR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00099 | hp2 | a0013 | c0013 | t0011 | g0190 | EUR | GBR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00140 | hp1 | a0003 | c0003 | t0004 | g0214 | EUR | GBR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0015 | EUR | GBR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00280 | hp1 | a0003 | c0003 | t0004 | g0219 | EUR | FIN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0018 | EUR | FIN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00323 | hp1 | a0009 | c0009 | t0016 | g0105 | EUR | FIN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0091 | EUR | FIN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00408 | hp1 | a0001 | c0001 | t0023 | g0168 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00597 | hp2 | a0008 | c0008 | t0001 | g0005 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00639 | hp2 | a0001 | c0001 | t0006 | g0075 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0330 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00642 | hp2 | a0005 | c0005 | t0002 | g0066 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0336 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00733 | hp2 | a0003 | c0003 | t0004 | g0208 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0072 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0311 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00741 | hp1 | a0002 | c0002 | t0009 | g0242 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG00741 | hp2 | a0002 | c0010 | t0001 | g0012 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01069 | hp1 | a0002 | c0010 | t0001 | g0233 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01069 | hp2 | a0005 | c0005 | t0001 | g0039 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01071 | hp1 | a0005 | c0005 | t0001 | g0039 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01081 | hp1 | a0003 | c0003 | t0004 | g0209 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01081 | hp2 | a0003 | c0003 | t0004 | g0221 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0284 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01099 | hp2 | a0005 | c0005 | t0001 | g0195 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01106 | hp1 | a0013 | c0013 | t0011 | g0191 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01106 | hp2 | a0002 | c0010 | t0001 | g0012 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01109 | hp1 | a0002 | c0010 | t0001 | g0012 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0296 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01167 | hp1 | a0001 | c0001 | t0006 | g0070 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01167 | hp2 | a0006 | c0006 | t0001 | g0061 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0335 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01168 | hp2 | a0002 | c0002 | t0009 | g0045 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01169 | hp1 | a0002 | c0002 | t0009 | g0045 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01169 | hp2 | a0006 | c0006 | t0001 | g0061 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01175 | hp1 | a0009 | c0009 | t0003 | g0102 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01192 | hp2 | a0005 | c0005 | t0002 | g0067 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01243 | hp2 | a0004 | c0004 | t0005 | g0119 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0016 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0302 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01256 | hp1 | a0003 | c0003 | t0004 | g0197 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0054 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0137 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01257 | hp2 | a0009 | c0009 | t0003 | g0026 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01258 | hp2 | a0009 | c0009 | t0003 | g0026 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01261 | hp1 | a0007 | c0007 | t0007 | g0009 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0264 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01358 | hp1 | a0003 | c0003 | t0004 | g0213 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01361 | hp1 | a0002 | c0010 | t0001 | g0012 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0295 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0073 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01496 | hp1 | a0004 | c0004 | t0005 | g0110 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01515 | hp1 | a0003 | c0003 | t0004 | g0041 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0069 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01516 | hp1 | a0009 | c0009 | t0003 | g0106 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01516 | hp2 | a0017 | c0024 | t0001 | g0015 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01517 | hp1 | a0003 | c0003 | t0004 | g0041 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0015 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01884 | hp1 | a0004 | c0004 | t0005 | g0118 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01884 | hp2 | a0003 | c0003 | t0004 | g0202 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01891 | hp2 | a0004 | c0004 | t0005 | g0001 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01928 | hp2 | a0003 | c0003 | t0004 | g0224 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0342 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01943 | hp2 | a0003 | c0003 | t0004 | g0217 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01952 | hp2 | a0003 | c0003 | t0004 | g0215 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01978 | hp1 | a0003 | c0003 | t0004 | g0218 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01978 | hp2 | a0002 | c0002 | t0009 | g0243 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0341 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01981 | hp2 | a0001 | c0001 | t0021 | g0156 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01993 | hp1 | a0003 | c0003 | t0004 | g0207 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0339 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02040 | hp2 | a0016 | c0023 | t0001 | g0005 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02055 | hp1 | a0004 | c0004 | t0005 | g0001 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02055 | hp2 | a0007 | c0007 | t0007 | g0081 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02148 | hp2 | a0003 | c0003 | t0004 | g0206 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | CDX | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | CDX | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | CDX | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02165 | hp2 | a0014 | c0020 | t0001 | g0013 | EAS | CDX | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02257 | hp1 | a0004 | c0004 | t0005 | g0001 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0334 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02258 | hp1 | a0003 | c0003 | t0004 | g0200 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0277 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0319 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02280 | hp1 | a0001 | c0001 | t0010 | g0104 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0345 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0338 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02300 | hp1 | a0003 | c0003 | t0004 | g0042 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02300 | hp2 | a0003 | c0003 | t0004 | g0042 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02451 | hp1 | a0004 | c0004 | t0005 | g0001 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02451 | hp2 | a0003 | c0003 | t0004 | g0198 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02572 | hp2 | a0005 | c0005 | t0001 | g0074 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0309 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0333 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0321 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02622 | hp1 | a0005 | c0005 | t0001 | g0196 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02622 | hp2 | a0010 | c0012 | t0001 | g0227 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02630 | hp1 | a0007 | c0007 | t0007 | g0079 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02630 | hp2 | a0005 | c0005 | t0011 | g0354 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02647 | hp1 | a0007 | c0007 | t0007 | g0078 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02647 | hp2 | a0003 | c0003 | t0004 | g0232 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02683 | hp1 | a0006 | c0006 | t0001 | g0347 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02683 | hp2 | a0004 | c0004 | t0007 | g0125 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0327 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02717 | hp1 | a0004 | c0004 | t0005 | g0113 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02717 | hp2 | a0005 | c0005 | t0001 | g0038 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02723 | hp2 | a0005 | c0005 | t0001 | g0037 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0273 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0278 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02738 | hp1 | a0007 | c0007 | t0007 | g0080 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0268 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02809 | hp1 | a0004 | c0004 | t0005 | g0001 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02809 | hp2 | a0005 | c0005 | t0015 | g0065 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02818 | hp2 | a0010 | c0012 | t0001 | g0226 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02886 | hp1 | a0001 | c0014 | t0001 | g0229 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0324 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02895 | hp1 | a0003 | c0003 | t0004 | g0040 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02895 | hp2 | a0003 | c0003 | t0004 | g0201 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02896 | hp1 | a0007 | c0007 | t0007 | g0009 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02896 | hp2 | a0005 | c0011 | t0001 | g0022 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02897 | hp1 | a0003 | c0003 | t0004 | g0040 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02897 | hp2 | a0005 | c0011 | t0001 | g0022 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02922 | hp1 | a0004 | c0004 | t0005 | g0112 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02922 | hp2 | a0005 | c0005 | t0001 | g0193 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0315 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02965 | hp2 | a0010 | c0012 | t0020 | g0228 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02970 | hp1 | a0004 | c0004 | t0002 | g0028 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02970 | hp2 | a0007 | c0007 | t0004 | g0121 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02976 | hp1 | a0004 | c0004 | t0005 | g0001 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02976 | hp2 | a0004 | c0004 | t0005 | g0111 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0138 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0308 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03041 | hp1 | a0003 | c0003 | t0004 | g0205 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03041 | hp2 | a0005 | c0011 | t0001 | g0071 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03098 | hp1 | a0010 | c0012 | t0001 | g0225 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03098 | hp2 | a0004 | c0004 | t0005 | g0115 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03130 | hp1 | a0001 | c0014 | t0001 | g0230 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03139 | hp1 | a0004 | c0004 | t0005 | g0001 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03195 | hp1 | a0004 | c0004 | t0005 | g0001 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03195 | hp2 | a0003 | c0003 | t0004 | g0199 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0323 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0257 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03453 | hp1 | a0005 | c0005 | t0002 | g0068 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0343 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03486 | hp2 | a0007 | c0007 | t0007 | g0009 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03491 | hp1 | a0012 | c0015 | t0001 | g0254 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0186 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0276 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0185 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03516 | hp1 | a0003 | c0003 | t0004 | g0203 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03540 | hp2 | a0007 | c0007 | t0007 | g0009 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03579 | hp1 | a0004 | c0004 | t0005 | g0123 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03579 | hp2 | a0004 | c0004 | t0005 | g0117 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0255 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0136 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0301 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03688 | hp1 | a0006 | c0006 | t0001 | g0349 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0317 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0307 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0258 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03710 | hp2 | a0002 | c0002 | t0013 | g0048 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03831 | hp1 | a0003 | c0003 | t0012 | g0211 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0141 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03834 | hp1 | a0003 | c0003 | t0007 | g0220 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0318 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03927 | hp2 | a0003 | c0025 | t0012 | g0212 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0332 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG04184 | hp1 | a0005 | c0005 | t0001 | g0194 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG04184 | hp2 | a0012 | c0015 | t0001 | g0048 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG04199 | hp1 | a0001 | c0001 | t0018 | g0058 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0303 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0328 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0256 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18522 | hp1 | a0006 | c0006 | t0001 | g0063 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18522 | hp2 | a0020 | c0017 | t0022 | g0320 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | CHB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | CHB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | CHB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18906 | hp1 | a0004 | c0004 | t0005 | g0001 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18906 | hp2 | a0006 | c0006 | t0010 | g0222 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18945 | hp1 | a0015 | c0022 | t0001 | g0285 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18949 | hp2 | a0018 | c0018 | t0002 | g0131 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18950 | hp2 | a0019 | c0019 | t0002 | g0306 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18956 | hp1 | a0008 | c0008 | t0001 | g0135 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18971 | hp1 | a0011 | c0016 | t0001 | g0013 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18974 | hp1 | a0002 | c0002 | t0017 | g0298 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18975 | hp1 | a0008 | c0008 | t0001 | g0029 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18982 | hp1 | a0006 | c0006 | t0001 | g0348 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0352 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18992 | hp2 | a0008 | c0008 | t0001 | g0005 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18998 | hp1 | a0002 | c0002 | t0019 | g0144 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19030 | hp1 | a0003 | c0003 | t0004 | g0204 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19030 | hp2 | a0004 | c0004 | t0001 | g0124 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19043 | hp1 | a0005 | c0005 | t0001 | g0037 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19059 | hp1 | a0008 | c0008 | t0001 | g0130 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19064 | hp2 | a0008 | c0008 | t0001 | g0147 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19085 | hp1 | a0001 | c0001 | t0024 | g0036 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19085 | hp2 | a0008 | c0008 | t0001 | g0146 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19089 | hp1 | a0008 | c0008 | t0001 | g0005 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19089 | hp2 | a0011 | c0016 | t0001 | g0252 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19240 | hp1 | a0004 | c0004 | t0002 | g0028 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA19240 | hp2 | a0004 | c0004 | t0005 | g0116 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA20129 | hp1 | a0005 | c0005 | t0001 | g0192 | AFR | ASW | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA20129 | hp2 | a0004 | c0004 | t0005 | g0122 | AFR | ASW | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0300 | EUR | TSI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | TSI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA20805 | hp1 | a0003 | c0003 | t0004 | g0210 | EUR | TSI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0238 | EUR | TSI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0331 | SAS | GIH | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0247 | SAS | GIH | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01123 | hp1 | a0002 | c0002 | t0014 | g0288 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0340 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02109 | hp1 | a0006 | c0006 | t0001 | g0223 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02109 | hp2 | a0005 | c0005 | t0002 | g0064 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02486 | hp1 | a0002 | c0021 | t0001 | g0052 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02486 | hp2 | a0006 | c0006 | t0001 | g0043 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0344 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0103 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG03471 | hp2 | a0004 | c0004 | t0005 | g0114 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG06807 | hp1 | a0006 | c0006 | t0001 | g0043 | AFR | USA | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
HG06807 | hp2 | a0005 | c0005 | t0001 | g0038 | AFR | USA | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA20300 | hp1 | a0004 | c0004 | t0005 | g0001 | AFR | USA | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA20300 | hp2 | a0003 | c0003 | t0004 | g0216 | AFR | USA | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
NA21309 | hp2 | a0005 | c0011 | t0001 | g0077 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0279 | REF | REF | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0310 | REF | REF | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:30610873
|
A | G | 2 | a0003a0006 | 43 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(40): Show |
missense_variant&splice_region_variant | MODERATE | c.67A>G | p.Ile23Val | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/9 | 225/2192 | 67/1284 | 23/427 | chr22 | 30610873 | ||
chr22:30610895
|
T | G | 1 | a0020 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.89T>G | p.Leu30Arg | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/9 | 247/2192 | 89/1284 | 30/427 | chr22 | 30610895 | ||
chr22:30611036
|
A | T | 1 | a0008 | 8 | HG00597.hp2 NA18956.hp1 NA18975.hp1 others(5): Show |
missense_variant | MODERATE | c.230A>T | p.Lys77Met | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/9 | 388/2192 | 230/1284 | 77/427 | chr22 | 30611036 | ||
chr22:30612880
|
T | C | 1 | a0013 | 2 | HG00099.hp2 HG01106.hp1 |
missense_variant | MODERATE | c.265T>C | p.Phe89Leu | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 423/2192 | 265/1284 | 89/427 | chr22 | 30612880 | ||
chr22:30612901
|
T | A | 1 | a0018 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.286T>A | p.Cys96Ser | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 444/2192 | 286/1284 | 96/427 | chr22 | 30612901 | ||
chr22:30612902
|
G | A | 1 | a0019 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.287G>A | p.Cys96Tyr | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 445/2192 | 287/1284 | 96/427 | chr22 | 30612902 | ||
chr22:30613037
|
C | G | 1 | a0017 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.422C>G | p.Ala141Gly | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 580/2192 | 422/1284 | 141/427 | chr22 | 30613037 | ||
chr22:30613039
|
A | G | 1 | a0016 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.424A>G | p.Ile142Val | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 582/2192 | 424/1284 | 142/427 | chr22 | 30613039 | ||
chr22:30614430
|
G | A | 1 | a0014 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.509G>A | p.Arg170Gln | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/9 | 667/2192 | 509/1284 | 170/427 | chr22 | 30614430 | ||
chr22:30614475
|
C | T | 1 | a0010 | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.554C>T | p.Pro185Leu | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/9 | 712/2192 | 554/1284 | 185/427 | chr22 | 30614475 | ||
chr22:30615363
|
C | T | 2 | a0004a0020 | 27 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(24): Show |
missense_variant | MODERATE | c.643C>T | p.Arg215Trp | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 5/9 | 801/2192 | 643/1284 | 215/427 | chr22 | 30615363 | ||
chr22:30615623
|
G | C | 9 | a0001a0003a0004others(6): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
missense_variant | MODERATE | c.776G>C | p.Arg259Pro | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/9 | 934/2192 | 776/1284 | 259/427 | chr22 | 30615623 | ||
chr22:30615704
|
C | T | 1 | a0015 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.857C>T | p.Ala286Val | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/9 | 1015/2192 | 857/1284 | 286/427 | chr22 | 30615704 | ||
chr22:30617387
|
C | T | 2 | a0011a0014 | 3 | HG02165.hp2 NA18971.hp1 NA19089.hp2 |
missense_variant | MODERATE | c.998C>T | p.Thr333Met | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/9 | 1156/2192 | 998/1284 | 333/427 | chr22 | 30617387 | ||
chr22:30617432
|
C | T | 2 | a0003a0007 | 42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
missense_variant | MODERATE | c.1043C>T | p.Ser348Phe | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/9 | 1201/2192 | 1043/1284 | 348/427 | chr22 | 30617432 | ||
chr22:30622988
|
T | C | 1 | a0009 | 5 | HG00323.hp1 HG01175.hp1 HG01257.hp2 others(2): Show |
missense_variant | MODERATE | c.1127T>C | p.Leu376Ser | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/9 | 1285/2192 | 1127/1284 | 376/427 | chr22 | 30622988 | ||
chr22:30623011
|
G | A | 1 | a0012 | 2 | HG03491.hp1 HG04184.hp2 |
missense_variant | MODERATE | c.1150G>A | p.Val384Met | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/9 | 1308/2192 | 1150/1284 | 384/427 | chr22 | 30623011 | ||
chr22:30623057
|
G | A | 2 | a0005a0013 | 24 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(21): Show |
missense_variant | MODERATE | c.1196G>A | p.Arg399Gln | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/9 | 1354/2192 | 1196/1284 | 399/427 | chr22 | 30623057 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:30612975
|
G | A | 1 | a0005c0011 | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.360G>A | p.Arg120Arg | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 518/2192 | 360/1284 | 120/427 | chr22 | 30612975 | ||
chr22:30614422
|
C | T | 1 | a0003c0025 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.501C>T | p.His167His | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/9 | 659/2192 | 501/1284 | 167/427 | chr22 | 30614422 | ||
chr22:30615687
|
T | C | 1 | a0001c0014 | 2 | HG02886.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.840T>C | p.Asp280Asp | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/9 | 998/2192 | 840/1284 | 280/427 | chr22 | 30615687 | ||
chr22:30615724
|
C | T | 1 | a0002c0021 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.877C>T | p.Leu293Leu | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/9 | 1035/2192 | 877/1284 | 293/427 | chr22 | 30615724 | ||
chr22:30617412
|
G | A | 1 | a0002c0010 | 5 | HG00741.hp2 HG01069.hp1 HG01106.hp2 others(2): Show |
synonymous_variant | LOW | c.1023G>A | p.Pro341Pro | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/9 | 1181/2192 | 1023/1284 | 341/427 | chr22 | 30617412 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:30626550
|
C | A | 1 | a0002c0002t0009 | 4 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*29C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 29 | chr22 | 30626550 | |||||
chr22:30626590
|
T | C | 1 | a0002c0002t0013 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*69T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 69 | chr22 | 30626590 | |||||
chr22:30626603
|
C | T | 7 | a0003c0003t0004a0003c0003t0007a0003c0003t0012others(4): Show | 43 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*82C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 82 | chr22 | 30626603 | |||||
chr22:30626648
|
C | T | 1 | a0001c0001t0006 | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*127C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 127 | chr22 | 30626648 | |||||
chr22:30626730
|
G | C | 1 | a0002c0002t0014 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*209G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 209 | chr22 | 30626730 | |||||
chr22:30626733
|
G | A | 1 | a0005c0005t0015 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*212G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 212 | chr22 | 30626733 | |||||
chr22:30626746
|
A | T | 10 | a0001c0001t0002a0001c0001t0021a0001c0001t0023others(7): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*225A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 225 | chr22 | 30626746 | |||||
chr22:30626804
|
C | G | 1 | a0010c0012t0020 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 283 | chr22 | 30626804 | |||||
chr22:30626821
|
T | G | 1 | a0009c0009t0016 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 300 | chr22 | 30626821 | |||||
chr22:30626828
|
C | CA | 8 | a0001c0001t0018a0001c0001t0021a0002c0002t0017others(5): Show | 44 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*313dupA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 314 | INFO_REALIGN_3_PRIME | chr22 | 30626828 | ||||
chr22:30626836
|
G | A | 1 | a0020c0017t0022 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 315 | chr22 | 30626836 | |||||
chr22:30626903
|
C | T | 2 | a0005c0005t0011a0013c0013t0011 | 3 | HG00099.hp2 HG01106.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*382C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 382 | chr22 | 30626903 | |||||
chr22:30626912
|
G | A | 1 | a0002c0002t0019 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 391 | chr22 | 30626912 | |||||
chr22:30626926
|
T | C | 1 | a0001c0001t0023 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 405 | chr22 | 30626926 | |||||
chr22:30626965
|
C | T | 7 | a0001c0001t0003a0001c0001t0010a0001c0001t0018others(4): Show | 95 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*444C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 444 | chr22 | 30626965 | |||||
chr22:30627204
|
A | G | 11 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(8): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*683A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 683 | chr22 | 30627204 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:30607406
|
C | T | 1 | a0005c0005t0011g0354 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64+11C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607406 | ||||||
chr22:30607467
|
A | G | 10 | a0001c0001t0002g0346a0002c0002t0001g0062a0002c0002t0001g0350others(7): Show | 12 | HG00597.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+72A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607467 | ||||||
chr22:30607474
|
T | C | 2 | a0001c0001t0001g0019a0006c0006t0001g0063 | 3 | HG01496.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64+79T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607474 | ||||||
chr22:30607574
|
A | G | 35 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(32): Show | 37 | HG00642.hp1 HG00733.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.64+179A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607574 | ||||||
chr22:30607620
|
G | A | 5 | a0005c0005t0002g0064a0005c0005t0002g0066a0005c0005t0002g0067others(2): Show | 5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+225G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607620 | ||||||
chr22:30607689
|
C | T | 2 | a0001c0001t0002g0313a0001c0001t0002g0314 | 2 | NA18975.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.64+294C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607689 | ||||||
chr22:30607927
|
A | G | 1 | a0001c0001t0002g0312 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64+532A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607927 | ||||||
chr22:30608140
|
G | A | 85 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(82): Show | 105 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.64+745G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608140 | ||||||
chr22:30608201
|
G | C | 108 | a0001c0001t0001g0019a0001c0001t0002g0002a0001c0001t0002g0006others(105): Show | 148 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.64+806G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608201 | ||||||
chr22:30608469
|
C | T | 1 | a0002c0002t0001g0057 | 2 | NA19006.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.64+1074C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608469 | ||||||
chr22:30608526
|
C | CTGCATGT others(31): Show |
3 | a0001c0001t0002g0027a0001c0001t0002g0108a0001c0001t0002g0109 | 4 | HG01070.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1133_64+1170dup others(38): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 30608526 | |||||
chr22:30608610
|
G | A | 11 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0039others(8): Show | 14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+1215G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608610 | ||||||
chr22:30608639
|
G | C | 165 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(162): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.64+1244G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608639 | ||||||
chr22:30608824
|
C | T | 1 | a0001c0001t0001g0019 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.64+1429C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608824 | ||||||
chr22:30608826
|
C | T | 1 | a0003c0003t0004g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.64+1431C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608826 | ||||||
chr22:30608841
|
C | G | 11 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0039others(8): Show | 14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+1446C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608841 | ||||||
chr22:30608858
|
T | G | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | NA19011.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.64+1463T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608858 | ||||||
chr22:30608877
|
C | T | 1 | a0002c0002t0001g0311 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.64+1482C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608877 | ||||||
chr22:30609001
|
G | A | 2 | a0002c0010t0001g0012a0002c0010t0001g0233 | 5 | HG00741.hp2 HG01069.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+1606G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609001 | ||||||
chr22:30609023
|
T | C | 17 | a0001c0001t0002g0120a0004c0004t0001g0124a0004c0004t0002g0028others(14): Show | 27 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.64+1628T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609023 | ||||||
chr22:30609031
|
A | G | 67 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(64): Show | 79 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.64+1636A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609031 | ||||||
chr22:30609141
|
C | T | 1 | a0002c0002t0001g0056 | 2 | NA18946.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.65-1730C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609141 | ||||||
chr22:30609153
|
C | G | 1 | a0001c0001t0008g0345 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-1718C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609153 | ||||||
chr22:30609159
|
CT | C | 19 | a0001c0001t0003g0082a0001c0001t0003g0316a0001c0001t0006g0069others(16): Show | 19 | HG00099.hp2 HG01167.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.65-1698delT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 30609159 | |||||
chr22:30609233
|
G | A | 1 | a0013c0013t0011g0190 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.65-1638G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609233 | ||||||
chr22:30609234
|
G | C | 3 | a0001c0001t0003g0023a0001c0001t0003g0083a0001c0001t0003g0084 | 4 | HG02040.hp1 HG02132.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1637G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609234 | ||||||
chr22:30609241
|
G | A | 2 | a0001c0001t0003g0317a0001c0001t0003g0318 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.65-1630G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609241 | ||||||
chr22:30609246
|
TCCCACCT others(3): Show |
T | 1 | a0001c0001t0003g0316 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.65-1622_65-1613del others(10): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 30609246 | |||||
chr22:30609257
|
C | A | 11 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0039others(8): Show | 14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.65-1614C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609257 | ||||||
chr22:30609263
|
A | G | 14 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230others(11): Show | 17 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-1608A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609263 | ||||||
chr22:30609306
|
G | A | 141 | a0001c0001t0001g0089a0001c0001t0001g0231a0001c0001t0003g0010others(138): Show | 169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.65-1565G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609306 | ||||||
chr22:30609350
|
T | C | 1 | a0001c0001t0003g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.65-1521T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609350 | ||||||
chr22:30609525
|
C | T | 1 | a0001c0001t0002g0189 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.65-1346C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609525 | ||||||
chr22:30609527
|
G | C | 5 | a0005c0005t0002g0064a0005c0005t0002g0066a0005c0005t0002g0067others(2): Show | 5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-1344G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609527 | ||||||
chr22:30609547
|
C | A | 1 | a0002c0002t0001g0239 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.65-1324C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609547 | ||||||
chr22:30609589
|
AGG | A | 278 | a0001c0001t0001g0019a0001c0001t0001g0231a0001c0001t0002g0002others(275): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.65-1277_65-1276del others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 30609589 | |||||
chr22:30609613
|
A | G | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1258A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609613 | ||||||
chr22:30609879
|
T | C | 3 | a0005c0005t0011g0354a0013c0013t0011g0190a0013c0013t0011g0191 | 3 | HG00099.hp2 HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.65-992T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609879 | ||||||
chr22:30609971
|
C | T | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-900C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609971 | ||||||
chr22:30610000
|
A | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0188a0001c0001t0024g0036 | 3 | HG00673.hp1 HG02165.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.65-871A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610000 | ||||||
chr22:30610017
|
C | T | 11 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0039others(8): Show | 14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.65-854C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610017 | ||||||
chr22:30610193
|
A | G | 1 | a0002c0002t0001g0309 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.65-678A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610193 | ||||||
chr22:30610254
|
A | G | 1 | a0004c0004t0005g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-617A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610254 | ||||||
chr22:30610283
|
C | A | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-588C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610283 | ||||||
chr22:30610518
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0187 | 6 | NA18944.hp2 NA18952.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-353C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610518 | ||||||
chr22:30610541
|
C | A | 2 | a0002c0002t0001g0044a0002c0002t0001g0240 | 3 | NA18972.hp1 NA19056.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.65-330C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610541 | ||||||
chr22:30610543
|
A | G | 1 | a0003c0003t0004g0224 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.65-328A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610543 | ||||||
chr22:30610565
|
G | A | 25 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(22): Show | 34 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.65-306G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610565 | ||||||
chr22:30610626
|
C | CT | 5 | a0007c0007t0007g0009a0007c0007t0007g0078a0007c0007t0007g0079others(2): Show | 8 | HG01261.hp1 HG02055.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-244dupT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 30610626 | |||||
chr22:30610639
|
A | G | 2 | a0002c0002t0001g0307a0002c0002t0001g0308 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.65-232A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610639 | ||||||
chr22:30610644
|
C | A | 1 | a0004c0004t0005g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-227C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610644 | ||||||
chr22:30610715
|
T | G | 5 | a0001c0001t0006g0016a0001c0001t0006g0020a0001c0001t0006g0069others(2): Show | 8 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-156T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610715 | ||||||
chr22:30610728
|
A | G | 2 | a0002c0002t0001g0185a0002c0002t0001g0186 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.65-143A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610728 | ||||||
chr22:30610854
|
C | T | 2 | a0013c0013t0011g0190a0013c0013t0011g0191 | 2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.65-17C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610854 | ||||||
chr22:30611090
|
T | C | 1 | a0001c0001t0003g0319 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.257+27T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611090 | ||||||
chr22:30611157
|
A | C | 1 | a0006c0006t0001g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.257+94A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611157 | ||||||
chr22:30611201
|
G | A | 1 | a0002c0002t0001g0132 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.257+138G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611201 | ||||||
chr22:30611205
|
A | G | 1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.257+142A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611205 | ||||||
chr22:30611251
|
G | T | 2 | a0013c0013t0011g0190a0013c0013t0011g0191 | 2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.257+188G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611251 | ||||||
chr22:30611276
|
C | T | 1 | a0019c0019t0002g0306 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.257+213C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611276 | ||||||
chr22:30611305
|
A | G | 5 | a0007c0007t0007g0009a0007c0007t0007g0078a0007c0007t0007g0079others(2): Show | 8 | HG01261.hp1 HG02055.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+242A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611305 | ||||||
chr22:30611317
|
ACT | A | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+257_257+258del others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 30611317 | |||||
chr22:30611332
|
G | A | 1 | a0003c0003t0004g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.257+269G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611332 | ||||||
chr22:30611384
|
T | C | 2 | a0013c0013t0011g0190a0013c0013t0011g0191 | 2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.257+321T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611384 | ||||||
chr22:30611533
|
C | T | 3 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230 | 3 | HG02886.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.257+470C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611533 | ||||||
chr22:30611653
|
G | A | 2 | a0001c0001t0002g0133a0001c0001t0002g0134 | 2 | HG02074.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.257+590G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611653 | ||||||
chr22:30611750
|
C | T | 2 | a0001c0001t0008g0343a0001c0001t0008g0344 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.257+687C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611750 | ||||||
chr22:30611881
|
G | A | 1 | a0005c0005t0002g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.257+818G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611881 | ||||||
chr22:30611932
|
A | G | 84 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(81): Show | 104 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.257+869A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611932 | ||||||
chr22:30611949
|
AAAG | A | 39 | a0003c0003t0004g0040a0003c0003t0004g0041a0003c0003t0004g0042others(36): Show | 44 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.257+891_257+893del others(3): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 30611949 | |||||
chr22:30612138
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.258-735C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612138 | ||||||
chr22:30612168
|
C | T | 6 | a0001c0001t0002g0007a0001c0001t0002g0183a0001c0001t0002g0184others(3): Show | 10 | NA18951.hp2 NA18953.hp2 NA18975.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-705C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612168 | ||||||
chr22:30612245
|
T | TA | 36 | a0002c0002t0001g0241a0002c0002t0009g0045a0002c0002t0009g0242others(33): Show | 40 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.258-616dupA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 30612245 | |||||
chr22:30612245
|
TA | T | 59 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(56): Show | 84 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.258-616delA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 30612245 | |||||
chr22:30612252
|
A | T | 5 | a0005c0005t0002g0064a0005c0005t0002g0066a0005c0005t0002g0067others(2): Show | 5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-621A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612252 | ||||||
chr22:30612253
|
A | T | 68 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(65): Show | 81 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.258-620A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612253 | ||||||
chr22:30612254
|
A | T | 1 | a0002c0002t0001g0305 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.258-619A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612254 | ||||||
chr22:30612258
|
T | A | 1 | a0005c0005t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.258-615T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612258 | ||||||
chr22:30612259
|
A | T | 1 | a0018c0018t0002g0131 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.258-614A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612259 | ||||||
chr22:30612298
|
C | T | 21 | a0003c0003t0004g0041a0003c0003t0004g0042a0003c0003t0004g0197others(18): Show | 23 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.258-575C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612298 | ||||||
chr22:30612346
|
C | T | 61 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.258-527C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612346 | ||||||
chr22:30612449
|
C | A | 11 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0039others(8): Show | 14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.258-424C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612449 | ||||||
chr22:30612455
|
C | T | 8 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0039others(5): Show | 11 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.258-418C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612455 | ||||||
chr22:30612475
|
G | T | 3 | a0005c0005t0011g0354a0013c0013t0011g0190a0013c0013t0011g0191 | 3 | HG00099.hp2 HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.258-398G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612475 | ||||||
chr22:30612504
|
C | T | 1 | a0005c0005t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.258-369C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612504 | ||||||
chr22:30612511
|
C | G | 3 | a0005c0011t0001g0022a0005c0011t0001g0071a0005c0011t0001g0077 | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-362C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612511 | ||||||
chr22:30612531
|
CAA | C | 3 | a0005c0011t0001g0022a0005c0011t0001g0071a0005c0011t0001g0077 | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-341_258-340del others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612531 | ||||||
chr22:30612550
|
C | T | 7 | a0001c0001t0003g0060a0001c0001t0003g0319a0001c0001t0003g0338others(4): Show | 8 | HG01123.hp2 HG01943.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-323C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612550 | ||||||
chr22:30612660
|
G | T | 1 | a0001c0001t0001g0019 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.258-213G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612660 | ||||||
chr22:30612758
|
A | G | 21 | a0001c0001t0006g0016a0001c0001t0006g0020a0001c0001t0006g0021others(18): Show | 29 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-115A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612758 | ||||||
chr22:30612764
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.258-109T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612764 | ||||||
chr22:30612806
|
G | A | 8 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0039others(5): Show | 11 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.258-67G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612806 | ||||||
chr22:30612828
|
C | CG | 8 | a0001c0001t0002g0154a0001c0001t0003g0085a0001c0001t0003g0316others(5): Show | 8 | HG01175.hp1 HG01496.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-41dupG | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 30612828 | |||||
chr22:30613059
|
C | T | 2 | a0003c0003t0004g0204a0003c0003t0004g0205 | 2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.427+17C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613059 | ||||||
chr22:30613131
|
T | A | 66 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(63): Show | 78 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.427+89T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613131 | ||||||
chr22:30613191
|
G | A | 1 | a0001c0001t0006g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.427+149G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613191 | ||||||
chr22:30613191
|
G | C | 1 | a0001c0001t0002g0030 | 2 | NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.427+149G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613191 | ||||||
chr22:30613234
|
T | C | 1 | a0010c0012t0001g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.427+192T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613234 | ||||||
chr22:30613247
|
T | A | 1 | a0018c0018t0002g0131 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.427+205T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613247 | ||||||
chr22:30613284
|
G | C | 1 | a0001c0001t0001g0019 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.427+242G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613284 | ||||||
chr22:30613390
|
C | T | 136 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(133): Show | 161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.427+348C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613390 | ||||||
chr22:30613468
|
G | T | 1 | a0005c0005t0011g0354 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.427+426G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613468 | ||||||
chr22:30613674
|
T | C | 1 | a0005c0005t0001g0037 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.427+632T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613674 | ||||||
chr22:30613765
|
T | C | 81 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(78): Show | 117 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.428-584T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613765 | ||||||
chr22:30613831
|
C | G | 1 | a0002c0002t0001g0304 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.428-518C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613831 | ||||||
chr22:30613833
|
G | C | 200 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(197): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.428-516G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613833 | ||||||
chr22:30613852
|
C | T | 81 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(78): Show | 117 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.428-497C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613852 | ||||||
chr22:30613868
|
C | T | 1 | a0005c0005t0001g0039 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.428-481C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613868 | ||||||
chr22:30614132
|
C | T | 2 | a0002c0002t0001g0303a0020c0017t0022g0320 | 2 | HG04204.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.428-217C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30614132 | ||||||
chr22:30614253
|
G | A | 16 | a0004c0004t0001g0124a0004c0004t0002g0028a0004c0004t0005g0001others(13): Show | 26 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.428-96G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30614253 | ||||||
chr22:30614255
|
G | C | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.428-94G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30614255 | ||||||
chr22:30614318
|
G | A | 3 | a0005c0011t0001g0022a0005c0011t0001g0071a0005c0011t0001g0077 | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-31G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30614318 | ||||||
chr22:30614326
|
C | T | 4 | a0006c0006t0001g0043a0006c0006t0001g0063a0006c0006t0001g0223others(1): Show | 5 | HG02109.hp1 HG02486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-23C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30614326 | ||||||
chr22:30614569
|
C | G | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.580+68C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30614569 | ||||||
chr22:30614662
|
T | C | 217 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(214): Show | 279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.580+161T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30614662 | ||||||
chr22:30614765
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.580+264C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30614765 | ||||||
chr22:30614841
|
G | A | 1 | a0002c0002t0001g0351 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.580+340G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30614841 | ||||||
chr22:30614953
|
A | G | 1 | a0001c0001t0003g0318 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.581-348A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30614953 | ||||||
chr22:30615010
|
C | T | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.581-291C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30615010 | ||||||
chr22:30615023
|
TC | T | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-275delC | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 30615023 | |||||
chr22:30615082
|
G | T | 9 | a0001c0001t0006g0016a0001c0001t0006g0020a0001c0001t0006g0021others(6): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.581-219G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30615082 | ||||||
chr22:30615237
|
G | GC | 4 | a0001c0001t0002g0153a0003c0003t0004g0198a0003c0003t0004g0199others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-60dupC | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 30615237 | |||||
chr22:30615293
|
A | C | 73 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(70): Show | 107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
splice_region_variant&intron_variant | LOW | c.581-8A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30615293 | ||||||
chr22:30615293
|
A | T | 4 | a0001c0001t0002g0035a0001c0001t0002g0180a0001c0001t0002g0181others(1): Show | 5 | NA18962.hp1 NA18995.hp1 NA19072.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.581-8A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30615293 | ||||||
chr22:30615516
|
T | G | 1 | a0008c0008t0001g0135 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.753+43T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 5/8 | chr22 | 30615516 | ||||||
chr22:30615517
|
CAG | C | 30 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(27): Show | 33 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.753+45_753+46delAG | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 5/8 | chr22 | 30615517 | ||||||
chr22:30615570
|
T | C | 197 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(194): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.754-31T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 5/8 | chr22 | 30615570 | ||||||
chr22:30615571
|
T | A | 1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.754-30T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 5/8 | chr22 | 30615571 | ||||||
chr22:30615818
|
T | C | 3 | a0002c0002t0001g0136a0002c0002t0001g0185a0002c0002t0001g0186 | 3 | HG03491.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.940+31T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30615818 | ||||||
chr22:30615895
|
A | T | 299 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(296): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.940+108A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30615895 | ||||||
chr22:30615912
|
G | A | 1 | a0003c0003t0004g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.940+125G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30615912 | ||||||
chr22:30615919
|
C | T | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.940+132C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30615919 | ||||||
chr22:30615936
|
T | C | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.940+149T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30615936 | ||||||
chr22:30616012
|
A | G | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+225A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616012 | ||||||
chr22:30616025
|
T | TTGGA | 7 | a0001c0001t0003g0325a0001c0001t0003g0337a0001c0001t0008g0344others(4): Show | 7 | HG01106.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.940+285_940+288dup others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | |||||
chr22:30616025
|
TTGGA | T | 156 | a0001c0001t0001g0089a0001c0001t0002g0126a0001c0001t0002g0127others(153): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.940+285_940+288del others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | |||||
chr22:30616025
|
TTGGATGG others(1): Show |
T | 79 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(76): Show | 111 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.940+281_940+288del others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | |||||
chr22:30616025
|
TTGGATGG others(5): Show |
T | 26 | a0001c0001t0001g0019a0001c0001t0002g0155a0001c0001t0002g0312others(23): Show | 38 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.940+277_940+288del others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | |||||
chr22:30616025
|
TTGGATGG others(13): Show |
T | 2 | a0002c0002t0001g0245a0006c0006t0001g0063 | 2 | NA18522.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.940+269_940+288del others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | |||||
chr22:30616025
|
TTGGATGG others(17): Show |
T | 1 | a0006c0006t0001g0347 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.940+265_940+288del others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | |||||
chr22:30616025
|
TTGGATGG others(21): Show |
T | 39 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230others(36): Show | 45 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.940+261_940+288del others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | |||||
chr22:30616103
|
A | G | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.940+316A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616103 | ||||||
chr22:30616110
|
A | G | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+323A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616110 | ||||||
chr22:30616159
|
C | G | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+372C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616159 | ||||||
chr22:30616166
|
C | G | 1 | a0002c0002t0001g0299 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.940+379C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616166 | ||||||
chr22:30616190
|
A | C | 1 | a0001c0001t0002g0178 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.940+403A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616190 | ||||||
chr22:30616203
|
G | A | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.940+416G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616203 | ||||||
chr22:30616255
|
G | A | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.940+468G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616255 | ||||||
chr22:30616314
|
T | C | 2 | a0003c0003t0004g0204a0003c0003t0004g0205 | 2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.940+527T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616314 | ||||||
chr22:30616487
|
C | CA | 16 | a0001c0001t0002g0176a0001c0001t0002g0182a0001c0001t0003g0087others(13): Show | 16 | HG00735.hp1 HG02071.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.940+718dupA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616487 | |||||
chr22:30616487
|
C | CAA | 93 | a0001c0001t0001g0019a0001c0001t0001g0231a0001c0001t0002g0002others(90): Show | 125 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.940+717_940+718dup others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616487 | |||||
chr22:30616487
|
CA | C | 33 | a0001c0001t0003g0060a0001c0001t0003g0084a0001c0001t0003g0099others(30): Show | 36 | HG00642.hp2 HG01069.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.940+718delA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616487 | |||||
chr22:30616487
|
CAA | C | 14 | a0005c0005t0001g0038a0005c0005t0001g0039a0005c0005t0001g0074others(11): Show | 17 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.940+717_940+718del others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616487 | |||||
chr22:30616492
|
A | G | 4 | a0006c0006t0001g0043a0006c0006t0001g0063a0006c0006t0001g0223others(1): Show | 5 | HG02109.hp1 HG02486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.940+705A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616492 | ||||||
chr22:30616583
|
C | G | 1 | a0001c0001t0002g0155 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.941-747C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616583 | ||||||
chr22:30616594
|
A | G | 3 | a0003c0003t0004g0202a0003c0003t0004g0203a0007c0007t0004g0121 | 3 | HG01884.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.941-736A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616594 | ||||||
chr22:30616645
|
C | T | 1 | a0002c0010t0001g0233 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.941-685C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616645 | ||||||
chr22:30616680
|
A | G | 1 | a0001c0001t0008g0324 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.941-650A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616680 | ||||||
chr22:30616686
|
A | G | 9 | a0001c0001t0006g0016a0001c0001t0006g0020a0001c0001t0006g0021others(6): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.941-644A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616686 | ||||||
chr22:30616769
|
T | C | 197 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(194): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.941-561T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616769 | ||||||
chr22:30616811
|
A | G | 1 | a0004c0004t0002g0028 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.941-519A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616811 | ||||||
chr22:30616893
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0003g0086 | 2 | HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.941-437T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616893 | ||||||
chr22:30616969
|
CAG | C | 61 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.941-360_941-359del others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616969 | ||||||
chr22:30617073
|
C | G | 3 | a0005c0011t0001g0022a0005c0011t0001g0071a0005c0011t0001g0077 | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-257C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617073 | ||||||
chr22:30617093
|
GGGTGGTG others(36): Show |
G | 2 | a0001c0001t0003g0337a0003c0003t0004g0221 | 2 | HG01081.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.941-190_941-148del others(43): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30617093 | |||||
chr22:30617103
|
G | A | 2 | a0003c0003t0004g0041a0003c0003t0004g0197 | 3 | HG01256.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.941-227G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617103 | ||||||
chr22:30617151
|
A | T | 1 | a0001c0001t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.941-179A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617151 | ||||||
chr22:30617166
|
C | T | 2 | a0013c0013t0011g0190a0013c0013t0011g0191 | 2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.941-164C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617166 | ||||||
chr22:30617200
|
C | T | 6 | a0001c0001t0002g0035a0001c0001t0002g0126a0001c0001t0002g0127others(3): Show | 7 | NA18962.hp1 NA18995.hp1 NA19011.hp1 others(4): Show |
intron_variant | MODIFIER | c.941-130C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617200 | ||||||
chr22:30617309
|
G | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.941-21G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617309 | ||||||
chr22:30617309
|
G | C | 1 | a0001c0001t0002g0181 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.941-21G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617309 | ||||||
chr22:30617317
|
C | T | 2 | a0002c0002t0001g0128a0002c0002t0019g0144 | 2 | NA18960.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.941-13C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617317 | ||||||
chr22:30617562
|
G | A | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1106+67G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617562 | ||||||
chr22:30617588
|
C | T | 1 | a0002c0002t0001g0304 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1106+93C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617588 | ||||||
chr22:30617630
|
A | T | 1 | a0002c0002t0001g0057 | 2 | NA19006.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1106+135A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617630 | ||||||
chr22:30617681
|
T | A | 1 | a0008c0008t0001g0135 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1106+186T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617681 | ||||||
chr22:30617688
|
T | A | 1 | a0002c0002t0001g0046 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1106+193T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617688 | ||||||
chr22:30617689
|
G | C | 1 | a0002c0002t0001g0046 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1106+194G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617689 | ||||||
chr22:30617690
|
A | T | 1 | a0002c0002t0001g0046 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1106+195A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617690 | ||||||
chr22:30617788
|
G | T | 1 | a0001c0001t0001g0019 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1106+293G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617788 | ||||||
chr22:30617802
|
C | T | 5 | a0007c0007t0007g0009a0007c0007t0007g0078a0007c0007t0007g0079others(2): Show | 8 | HG01261.hp1 HG02055.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1106+307C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617802 | ||||||
chr22:30617809
|
A | T | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106+314A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617809 | ||||||
chr22:30617841
|
A | C | 1 | a0005c0005t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1106+346A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617841 | ||||||
chr22:30617934
|
G | T | 18 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230others(15): Show | 22 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1106+439G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617934 | ||||||
chr22:30618019
|
C | T | 3 | a0005c0005t0011g0354a0013c0013t0011g0190a0013c0013t0011g0191 | 3 | HG00099.hp2 HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1106+524C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618019 | ||||||
chr22:30618078
|
T | C | 1 | a0005c0005t0011g0354 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1106+583T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618078 | ||||||
chr22:30618113
|
A | AT | 8 | a0001c0001t0001g0231a0002c0002t0001g0029a0002c0002t0001g0142others(5): Show | 8 | HG00423.hp1 HG03225.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.1106+638dupT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30618113 | |||||
chr22:30618113
|
AT | A | 184 | a0001c0001t0001g0019a0001c0001t0002g0002a0001c0001t0002g0006others(181): Show | 238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1106+638delT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30618113 | |||||
chr22:30618113
|
ATT | A | 31 | a0001c0001t0001g0089a0001c0001t0002g0108a0001c0001t0002g0109others(28): Show | 40 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1106+637_1106+638d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30618113 | |||||
chr22:30618263
|
G | T | 1 | a0002c0002t0001g0296 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1106+768G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618263 | ||||||
chr22:30618272
|
G | T | 1 | a0008c0008t0001g0135 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1106+777G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618272 | ||||||
chr22:30618272
|
GT | G | 193 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(190): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1106+788delT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30618272 | |||||
chr22:30618273
|
T | G | 2 | a0002c0002t0001g0247a0002c0002t0001g0255 | 2 | HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1106+778T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618273 | ||||||
chr22:30618390
|
C | T | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1106+895C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618390 | ||||||
chr22:30618432
|
A | G | 18 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230others(15): Show | 22 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1106+937A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618432 | ||||||
chr22:30618433
|
C | T | 1 | a0003c0003t0007g0220 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1106+938C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618433 | ||||||
chr22:30618435
|
T | C | 1 | a0006c0006t0001g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1106+940T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618435 | ||||||
chr22:30618487
|
C | T | 212 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(209): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1106+992C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618487 | ||||||
chr22:30618497
|
G | A | 3 | a0003c0003t0007g0220a0004c0004t0001g0124a0004c0004t0002g0028 | 4 | HG02970.hp1 HG03834.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106+1002G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618497 | ||||||
chr22:30618526
|
A | G | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106+1031A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618526 | ||||||
chr22:30618567
|
T | A | 1 | a0002c0002t0001g0251 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1106+1072T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618567 | ||||||
chr22:30618585
|
G | A | 78 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(75): Show | 113 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1106+1090G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618585 | ||||||
chr22:30618659
|
A | C | 1 | a0002c0002t0001g0250 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1106+1164A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618659 | ||||||
chr22:30618674
|
C | T | 1 | a0002c0002t0001g0275 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1106+1179C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618674 | ||||||
chr22:30618680
|
G | C | 1 | a0001c0001t0001g0019 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1106+1185G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618680 | ||||||
chr22:30618730
|
A | G | 6 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0192others(3): Show | 8 | HG01099.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1106+1235A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618730 | ||||||
chr22:30618758
|
A | G | 1 | a0020c0017t0022g0320 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1106+1263A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618758 | ||||||
chr22:30618839
|
A | G | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1106+1344A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618839 | ||||||
chr22:30618873
|
G | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1106+1378G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618873 | ||||||
chr22:30618904
|
G | A | 61 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1106+1409G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618904 | ||||||
chr22:30619012
|
T | C | 9 | a0001c0001t0006g0016a0001c0001t0006g0020a0001c0001t0006g0021others(6): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1106+1517T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619012 | ||||||
chr22:30619116
|
A | T | 1 | a0004c0004t0005g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1106+1621A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619116 | ||||||
chr22:30619231
|
C | G | 3 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230 | 3 | HG02886.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1106+1736C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619231 | ||||||
chr22:30619243
|
A | G | 1 | a0003c0003t0004g0219 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1106+1748A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619243 | ||||||
chr22:30619251
|
A | T | 1 | a0001c0001t0010g0104 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1106+1756A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619251 | ||||||
chr22:30619359
|
C | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1106+1864C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619359 | ||||||
chr22:30619395
|
A | C | 1 | a0003c0003t0004g0040 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1106+1900A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619395 | ||||||
chr22:30619420
|
C | T | 2 | a0002c0002t0001g0014a0002c0002t0001g0274 | 5 | NA18944.hp1 NA18963.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.1106+1925C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619420 | ||||||
chr22:30619426
|
T | C | 1 | a0001c0001t0003g0326 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1106+1931T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619426 | ||||||
chr22:30619514
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1106+2019G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619514 | ||||||
chr22:30619575
|
G | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1106+2080G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619575 | ||||||
chr22:30619586
|
C | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1106+2091C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619586 | ||||||
chr22:30619617
|
C | T | 1 | a0001c0001t0003g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1106+2122C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619617 | ||||||
chr22:30619671
|
G | C | 1 | a0004c0004t0005g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1106+2176G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619671 | ||||||
chr22:30619733
|
C | T | 31 | a0003c0003t0004g0040a0003c0003t0004g0041a0003c0003t0004g0042others(28): Show | 34 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1106+2238C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619733 | ||||||
chr22:30619755
|
G | A | 2 | a0002c0002t0001g0284a0002c0002t0001g0300 | 2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1106+2260G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619755 | ||||||
chr22:30619814
|
T | C | 9 | a0002c0002t0001g0047a0002c0002t0001g0256a0002c0002t0001g0257others(6): Show | 10 | HG02602.hp2 HG02698.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1106+2319T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619814 | ||||||
chr22:30619951
|
T | C | 213 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(210): Show | 275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1106+2456T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619951 | ||||||
chr22:30619992
|
A | G | 5 | a0002c0002t0001g0236a0002c0002t0001g0253a0002c0002t0001g0270others(2): Show | 5 | HG00438.hp1 HG02071.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.1106+2497A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619992 | ||||||
chr22:30619998
|
A | T | 7 | a0001c0001t0003g0331a0001c0001t0003g0332a0001c0001t0003g0333others(4): Show | 7 | HG00733.hp1 HG01168.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1106+2503A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619998 | ||||||
chr22:30620020
|
G | C | 7 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0210others(4): Show | 7 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1106+2525G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620020 | ||||||
chr22:30620095
|
G | A | 24 | a0004c0004t0001g0124a0004c0004t0002g0028a0004c0004t0005g0001others(21): Show | 36 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1106+2600G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620095 | ||||||
chr22:30620114
|
G | A | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1106+2619G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620114 | ||||||
chr22:30620143
|
CT | C | 48 | a0001c0001t0001g0019a0001c0001t0002g0154a0001c0001t0002g0157others(45): Show | 55 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.1106+2663delT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30620143 | |||||
chr22:30620159
|
A | T | 3 | a0002c0002t0001g0238a0002c0002t0001g0295a0002c0002t0001g0296 | 3 | HG01109.hp2 HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1106+2664A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620159 | ||||||
chr22:30620258
|
C | T | 1 | a0010c0012t0001g0226 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1107-2710C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620258 | ||||||
chr22:30620259
|
C | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1107-2709C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620259 | ||||||
chr22:30620260
|
G | A | 2 | a0003c0003t0004g0204a0003c0003t0004g0205 | 2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1107-2708G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620260 | ||||||
chr22:30620423
|
C | T | 1 | a0002c0002t0001g0294 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1107-2545C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620423 | ||||||
chr22:30620511
|
C | T | 1 | a0008c0008t0001g0135 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1107-2457C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620511 | ||||||
chr22:30620552
|
T | G | 36 | a0003c0003t0004g0040a0003c0003t0004g0041a0003c0003t0004g0042others(33): Show | 42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1107-2416T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620552 | ||||||
chr22:30620658
|
A | G | 8 | a0006c0006t0001g0043a0006c0006t0001g0061a0006c0006t0001g0063others(5): Show | 10 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1107-2310A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620658 | ||||||
chr22:30620685
|
A | G | 4 | a0006c0006t0001g0043a0006c0006t0001g0063a0006c0006t0001g0223others(1): Show | 5 | HG02109.hp1 HG02486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1107-2283A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620685 | ||||||
chr22:30620760
|
C | T | 1 | a0002c0002t0001g0293 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1107-2208C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620760 | ||||||
chr22:30620786
|
C | T | 1 | a0001c0001t0002g0027 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1107-2182C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620786 | ||||||
chr22:30620854
|
A | T | 1 | a0001c0001t0002g0174 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1107-2114A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620854 | ||||||
chr22:30620914
|
G | C | 1 | a0001c0001t0002g0189 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1107-2054G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620914 | ||||||
chr22:30620924
|
A | G | 6 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0192others(3): Show | 8 | HG01099.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1107-2044A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620924 | ||||||
chr22:30620927
|
G | A | 31 | a0003c0003t0004g0040a0003c0003t0004g0041a0003c0003t0004g0042others(28): Show | 34 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1107-2041G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620927 | ||||||
chr22:30620963
|
C | G | 1 | a0001c0001t0003g0060 | 2 | NA19058.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1107-2005C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620963 | ||||||
chr22:30620986
|
G | GGGT | 24 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230others(21): Show | 28 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1107-1975_1107-197 others(7): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30620986 | |||||
chr22:30620996
|
T | G | 224 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0002g0002others(221): Show | 286 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1107-1972T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620996 | ||||||
chr22:30620999
|
T | G | 11 | a0001c0001t0001g0019a0001c0001t0002g0034a0001c0001t0002g0035others(8): Show | 15 | HG01346.hp2 HG01358.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1107-1969T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620999 | ||||||
chr22:30621317
|
C | T | 1 | a0002c0002t0001g0272 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1107-1651C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621317 | ||||||
chr22:30621332
|
A | C | 2 | a0001c0001t0001g0019a0004c0004t0007g0125 | 3 | HG01496.hp2 HG02683.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1107-1636A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621332 | ||||||
chr22:30621335
|
A | G | 100 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(97): Show | 121 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1107-1633A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621335 | ||||||
chr22:30621338
|
G | A | 1 | a0008c0008t0001g0146 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1107-1630G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621338 | ||||||
chr22:30621356
|
T | C | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1107-1612T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621356 | ||||||
chr22:30621381
|
A | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1107-1587A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621381 | ||||||
chr22:30621384
|
C | T | 3 | a0001c0001t0003g0059a0001c0001t0003g0316a0001c0001t0003g0337 | 4 | HG02071.hp2 NA18982.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1107-1584C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621384 | ||||||
chr22:30621411
|
T | C | 217 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(214): Show | 279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1107-1557T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621411 | ||||||
chr22:30621416
|
C | T | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1107-1552C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621416 | ||||||
chr22:30621417
|
G | A | 2 | a0013c0013t0011g0190a0013c0013t0011g0191 | 2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1107-1551G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621417 | ||||||
chr22:30621434
|
AG | A | 2 | a0002c0002t0001g0050a0002c0002t0001g0269 | 3 | NA18947.hp2 NA18960.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1107-1533delG | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621434 | ||||||
chr22:30621470
|
G | A | 76 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 111 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1107-1498G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621470 | ||||||
chr22:30621470
|
G | GTTA | 97 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0003g0010others(94): Show | 118 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1107-1496_1107-149 others(7): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30621470 | |||||
chr22:30621471
|
T | A | 1 | a0001c0001t0002g0173 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1107-1497T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621471 | ||||||
chr22:30621473
|
T | A | 3 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230 | 3 | HG02886.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1107-1495T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621473 | ||||||
chr22:30621476
|
TG | T | 3 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230 | 3 | HG02886.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1107-1491delG | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621476 | ||||||
chr22:30621480
|
T | A | 16 | a0004c0004t0001g0124a0004c0004t0002g0028a0004c0004t0005g0001others(13): Show | 26 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1107-1488T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621480 | ||||||
chr22:30621607
|
T | C | 2 | a0002c0002t0001g0142a0002c0002t0001g0143 | 2 | NA18955.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1107-1361T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621607 | ||||||
chr22:30621691
|
C | G | 54 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(51): Show | 78 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1107-1277C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621691 | ||||||
chr22:30621730
|
C | T | 23 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230others(20): Show | 27 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1107-1238C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621730 | ||||||
chr22:30621749
|
G | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1107-1219G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621749 | ||||||
chr22:30621753
|
G | T | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1107-1215G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621753 | ||||||
chr22:30621790
|
T | C | 100 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(97): Show | 121 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1107-1178T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621790 | ||||||
chr22:30621856
|
C | G | 5 | a0001c0001t0003g0011a0001c0001t0003g0085a0001c0001t0003g0097others(2): Show | 8 | NA18939.hp2 NA18942.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.1107-1112C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621856 | ||||||
chr22:30621899
|
C | A | 1 | a0005c0005t0015g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1107-1069C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621899 | ||||||
chr22:30621982
|
C | T | 1 | a0002c0002t0001g0292 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1107-986C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621982 | ||||||
chr22:30622029
|
C | G | 1 | a0001c0014t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1107-939C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622029 | ||||||
chr22:30622075
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1107-893C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622075 | ||||||
chr22:30622085
|
T | C | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1107-883T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622085 | ||||||
chr22:30622091
|
G | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1107-877G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622091 | ||||||
chr22:30622137
|
A | G | 23 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230others(20): Show | 27 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1107-831A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622137 | ||||||
chr22:30622238
|
T | C | 98 | a0001c0001t0001g0089a0001c0001t0001g0231a0001c0001t0003g0010others(95): Show | 118 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1107-730T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622238 | ||||||
chr22:30622574
|
T | G | 76 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(73): Show | 92 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1107-394T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622574 | ||||||
chr22:30622585
|
G | A | 5 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0210others(2): Show | 5 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1107-383G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622585 | ||||||
chr22:30622618
|
G | A | 1 | a0001c0001t0006g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1107-350G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622618 | ||||||
chr22:30622635
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1107-333C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622635 | ||||||
chr22:30622659
|
C | T | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1107-309C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622659 | ||||||
chr22:30622782
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1107-186G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622782 | ||||||
chr22:30622790
|
G | A | 225 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(222): Show | 289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1107-178G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622790 | ||||||
chr22:30622830
|
C | T | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1107-138C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622830 | ||||||
chr22:30622897
|
G | C | 69 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(66): Show | 82 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1107-71G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622897 | ||||||
chr22:30622904
|
A | T | 1 | a0002c0002t0001g0271 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1107-64A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622904 | ||||||
chr22:30623107
|
G | C | 1 | a0001c0001t0001g0019 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1222+24G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623107 | ||||||
chr22:30623199
|
A | C | 1 | a0006c0006t0001g0043 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1222+116A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623199 | ||||||
chr22:30623220
|
G | A | 1 | a0002c0002t0001g0351 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1222+137G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623220 | ||||||
chr22:30623247
|
G | GC | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1222+164_1222+165i others(3): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623247 | ||||||
chr22:30623248
|
A | C | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1222+165A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623248 | ||||||
chr22:30623296
|
CA | C | 120 | a0001c0001t0001g0231a0001c0001t0002g0002a0001c0001t0002g0006others(117): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1222+228delA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623296 | |||||
chr22:30623357
|
C | T | 1 | a0002c0002t0001g0268 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1222+274C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623357 | ||||||
chr22:30623371
|
A | G | 1 | a0001c0001t0002g0034 | 2 | HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1222+288A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623371 | ||||||
chr22:30623448
|
G | A | 1 | a0002c0002t0001g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1222+365G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623448 | ||||||
chr22:30623461
|
T | G | 8 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0039others(5): Show | 11 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+378T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623461 | ||||||
chr22:30623470
|
A | G | 95 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(92): Show | 115 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1222+387A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623470 | ||||||
chr22:30623562
|
AACTTTTC others(4): Show |
A | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+481_1222+491d others(13): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623562 | |||||
chr22:30623646
|
G | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1222+563G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623646 | ||||||
chr22:30623653
|
A | G | 5 | a0005c0005t0002g0064a0005c0005t0002g0066a0005c0005t0002g0067others(2): Show | 5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+570A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623653 | ||||||
chr22:30623692
|
T | C | 1 | a0001c0001t0003g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1222+609T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623692 | ||||||
chr22:30623699
|
A | AAT | 3 | a0005c0011t0001g0022a0005c0011t0001g0071a0005c0011t0001g0077 | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+628_1222+629d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623699 | |||||
chr22:30623699
|
AAT | A | 76 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(73): Show | 92 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1222+628_1222+629d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623699 | |||||
chr22:30623703
|
T | C | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+620T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623703 | ||||||
chr22:30623708
|
A | G | 16 | a0004c0004t0001g0124a0004c0004t0002g0028a0004c0004t0005g0001others(13): Show | 26 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1222+625A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623708 | ||||||
chr22:30623709
|
TATACAG | T | 2 | a0003c0003t0004g0040a0003c0003t0004g0201 | 3 | HG02895.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1222+628_1222+633d others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623709 | |||||
chr22:30623711
|
TAC | T | 5 | a0002c0002t0001g0255a0007c0007t0007g0009a0007c0007t0007g0078others(2): Show | 8 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222+630_1222+631d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623711 | |||||
chr22:30623711
|
TACAG | T | 34 | a0001c0001t0001g0019a0001c0001t0001g0231a0001c0014t0001g0229others(31): Show | 37 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1222+632_1222+635d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623711 | |||||
chr22:30623715
|
G | C | 1 | a0003c0003t0004g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1222+632G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623715 | ||||||
chr22:30623715
|
G | T | 4 | a0007c0007t0007g0009a0007c0007t0007g0078a0007c0007t0007g0079others(1): Show | 7 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+632G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623715 | ||||||
chr22:30623715
|
GAC | G | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+638_1222+639d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623715 | |||||
chr22:30623717
|
C | T | 1 | a0007c0007t0007g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1222+634C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623717 | ||||||
chr22:30623721
|
CAT | C | 4 | a0002c0002t0001g0056a0002c0002t0001g0264a0002c0002t0001g0265others(1): Show | 5 | HG00408.hp2 HG01074.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+645_1222+646d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623721 | |||||
chr22:30623725
|
T | C | 1 | a0005c0005t0015g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1222+642T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623725 | ||||||
chr22:30623733
|
T | TACATATA others(3): Show |
1 | a0004c0004t0005g0112 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1222+659_1222+660i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623733 | |||||
chr22:30623741
|
TATAC | T | 74 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(71): Show | 109 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1222+660_1222+663d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623741 | |||||
chr22:30623743
|
T | C | 1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1222+660T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623743 | ||||||
chr22:30623743
|
TAC | T | 74 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(71): Show | 90 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1222+666_1222+667d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623743 | |||||
chr22:30623745
|
C | CATATATA others(3): Show |
1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1222+663_1222+664i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623745 | |||||
chr22:30623749
|
CAT | C | 2 | a0005c0005t0001g0037a0005c0005t0001g0194 | 3 | HG02723.hp2 HG04184.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1222+673_1222+674d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623749 | |||||
chr22:30623753
|
T | TATATGTA others(247): Show |
1 | a0007c0007t0004g0121 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1222+679_1222+680i others(256): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623753 | |||||
chr22:30623753
|
T | TATGTATA others(259): Show |
1 | a0003c0003t0004g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1222+672_1222+673i others(268): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623753 | |||||
chr22:30623754
|
ATATG | A | 8 | a0003c0003t0004g0040a0003c0003t0004g0198a0003c0003t0004g0199others(5): Show | 9 | HG00642.hp2 HG01192.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+675_1222+678d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623754 | |||||
chr22:30623756
|
A | G | 3 | a0005c0005t0002g0064a0005c0005t0002g0068a0005c0005t0015g0065 | 3 | HG02109.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+673A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623756 | ||||||
chr22:30623757
|
T | C | 1 | a0004c0004t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1222+674T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623757 | ||||||
chr22:30623758
|
G | A | 5 | a0004c0004t0005g0112a0004c0004t0005g0118a0005c0005t0002g0064others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+675G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623758 | ||||||
chr22:30623758
|
GTA | G | 73 | a0001c0001t0001g0019a0002c0002t0001g0004a0002c0002t0001g0015others(70): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1222+686_1222+687d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623758 | |||||
chr22:30623758
|
GTATA | G | 3 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230 | 3 | HG02886.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1222+684_1222+687d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623758 | |||||
chr22:30623759
|
T | C | 2 | a0004c0004t0005g0112a0004c0004t0005g0118 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1222+676T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623759 | ||||||
chr22:30623760
|
A | G | 8 | a0003c0003t0004g0040a0003c0003t0004g0198a0003c0003t0004g0199others(5): Show | 9 | HG00642.hp2 HG01192.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+677A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623760 | ||||||
chr22:30623761
|
T | C | 2 | a0004c0004t0005g0112a0004c0004t0005g0118 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1222+678T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623761 | ||||||
chr22:30623763
|
T | C | 159 | a0001c0001t0001g0089a0001c0001t0002g0002a0001c0001t0002g0006others(156): Show | 213 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1222+680T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623763 | ||||||
chr22:30623765
|
T | C | 2 | a0003c0003t0004g0041a0003c0003t0004g0197 | 3 | HG01256.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1222+682T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623765 | ||||||
chr22:30623767
|
TATAC | T | 61 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1222+686_1222+689d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623767 | |||||
chr22:30623769
|
T | C | 2 | a0005c0005t0001g0194a0005c0005t0011g0354 | 2 | HG02630.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1222+686T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623769 | ||||||
chr22:30623769
|
T | TATGAAAT others(14): Show |
1 | a0006c0006t0001g0347 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1222+687_1222+688i others(23): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623769 | |||||
chr22:30623771
|
C | T | 67 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(64): Show | 79 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1222+688C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623771 | ||||||
chr22:30623773
|
CACAT | C | 8 | a0004c0004t0005g0112a0006c0006t0001g0043a0006c0006t0001g0061others(5): Show | 10 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1222+692_1222+695d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623773 | |||||
chr22:30623775
|
C | T | 4 | a0003c0003t0004g0202a0003c0003t0004g0203a0004c0004t0005g0118others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+692C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623775 | ||||||
chr22:30623777
|
T | C | 69 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(66): Show | 81 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1222+694T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623777 | ||||||
chr22:30623777
|
T | TATATACA others(3): Show |
6 | a0004c0004t0005g0001a0004c0004t0005g0111a0004c0004t0005g0116others(3): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1222+699_1222+700i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623777 | |||||
chr22:30623779
|
T | TATACAC | 2 | a0004c0004t0001g0124a0004c0004t0002g0028 | 3 | HG02970.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1222+699_1222+700i others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623779 | |||||
chr22:30623779
|
T | TATACACA others(1): Show |
4 | a0004c0004t0005g0110a0004c0004t0005g0113a0004c0004t0005g0114others(1): Show | 4 | HG01496.hp1 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+699_1222+700i others(10): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623779 | |||||
chr22:30623779
|
T | TATACACA others(15): Show |
1 | a0005c0005t0001g0037 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1222+699_1222+700i others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623779 | |||||
chr22:30623779
|
T | TATACACA others(297): Show |
2 | a0003c0003t0004g0202a0003c0003t0004g0203 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1222+699_1222+700i others(306): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623779 | |||||
chr22:30623780
|
A | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0172 | 3 | HG00423.hp2 NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1222+697A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623780 | ||||||
chr22:30623781
|
T | C | 4 | a0005c0005t0001g0194a0005c0011t0001g0022a0005c0011t0001g0071others(1): Show | 5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+698T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623781 | ||||||
chr22:30623782
|
A | G | 10 | a0001c0001t0003g0091a0001c0001t0006g0016a0001c0001t0006g0020others(7): Show | 14 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1222+699A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623782 | ||||||
chr22:30623782
|
ATG | A | 6 | a0005c0005t0002g0066a0005c0005t0002g0067a0005c0005t0011g0354others(3): Show | 6 | HG00099.hp2 HG00642.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+701_1222+702d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623782 | |||||
chr22:30623783
|
T | C | 9 | a0005c0005t0001g0038a0005c0005t0001g0039a0005c0005t0001g0074others(6): Show | 12 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+700T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623783 | ||||||
chr22:30623784
|
G | A | 40 | a0001c0001t0003g0091a0001c0001t0006g0016a0001c0001t0006g0020others(37): Show | 58 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.1222+701G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623784 | ||||||
chr22:30623785
|
T | C | 18 | a0004c0004t0005g0112a0004c0004t0005g0122a0005c0005t0001g0038others(15): Show | 20 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1222+702T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623785 | ||||||
chr22:30623787
|
T | C | 39 | a0001c0001t0003g0091a0001c0001t0006g0016a0001c0001t0006g0020others(36): Show | 55 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1222+704T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623787 | ||||||
chr22:30623789
|
C | T | 21 | a0001c0001t0003g0091a0001c0001t0006g0016a0001c0001t0006g0020others(18): Show | 28 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1222+706C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623789 | ||||||
chr22:30623793
|
T | C | 2 | a0005c0011t0001g0022a0005c0011t0001g0071 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1222+710T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623793 | ||||||
chr22:30623793
|
TATACACA others(1): Show |
T | 4 | a0001c0001t0002g0183a0007c0007t0007g0009a0007c0007t0007g0078others(1): Show | 7 | HG01261.hp1 HG02647.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+718_1222+725d others(10): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623793 | |||||
chr22:30623795
|
T | C | 7 | a0003c0003t0004g0202a0003c0003t0004g0203a0005c0005t0001g0038others(4): Show | 9 | HG01884.hp2 HG02717.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+712T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623795 | ||||||
chr22:30623795
|
T | TATAC | 65 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(62): Show | 77 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1222+713_1222+714i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623795 | |||||
chr22:30623795
|
TAC | T | 9 | a0003c0003t0004g0198a0003c0003t0004g0199a0003c0003t0004g0200others(6): Show | 9 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+718_1222+719d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623795 | |||||
chr22:30623797
|
C | T | 13 | a0004c0004t0001g0124a0004c0004t0002g0028a0004c0004t0005g0001others(10): Show | 23 | HG01243.hp2 HG01496.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1222+714C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623797 | ||||||
chr22:30623799
|
C | T | 2 | a0005c0011t0001g0022a0005c0011t0001g0071 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1222+716C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623799 | ||||||
chr22:30623801
|
C | CAT | 11 | a0001c0001t0003g0091a0001c0001t0006g0016a0001c0001t0006g0020others(8): Show | 15 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.1222+720_1222+721d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623801 | |||||
chr22:30623801
|
C | CATAT | 7 | a0002c0002t0001g0258a0004c0004t0002g0028a0004c0004t0007g0125others(4): Show | 8 | HG01099.hp2 HG01192.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222+721_1222+722i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623801 | |||||
chr22:30623801
|
C | T | 154 | a0001c0001t0001g0089a0001c0001t0001g0231a0001c0001t0002g0002others(151): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1222+718C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623801 | ||||||
chr22:30623803
|
T | C | 2 | a0001c0001t0002g0160a0019c0019t0002g0306 | 2 | HG00609.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1222+720T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623803 | ||||||
chr22:30623803
|
T | TATAC | 8 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222+721_1222+722i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | |||||
chr22:30623803
|
T | TATACACA others(13): Show |
2 | a0006c0006t0001g0061a0006c0006t0001g0349 | 3 | HG01167.hp2 HG01169.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1222+721_1222+722i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | |||||
chr22:30623803
|
T | TATATAC | 82 | a0001c0001t0001g0019a0001c0001t0002g0002a0001c0001t0002g0006others(79): Show | 120 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1222+721_1222+722i others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | |||||
chr22:30623803
|
T | TATATACA others(1): Show |
135 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(132): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1222+721_1222+722i others(10): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | |||||
chr22:30623803
|
T | TATATACA others(43): Show |
4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+721_1222+722i others(52): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | |||||
chr22:30623803
|
T | TATATATG others(27): Show |
1 | a0002c0002t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1222+721_1222+722i others(36): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | |||||
chr22:30623803
|
T | TATATATG others(59): Show |
1 | a0006c0006t0001g0347 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1222+721_1222+722i others(68): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | |||||
chr22:30623803
|
TACAC | T | 20 | a0001c0001t0002g0161a0001c0001t0021g0156a0003c0003t0004g0041others(17): Show | 22 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1222+722_1222+725d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | |||||
chr22:30623805
|
C | T | 14 | a0003c0003t0004g0198a0003c0003t0004g0199a0003c0003t0004g0200others(11): Show | 14 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1222+722C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623805 | ||||||
chr22:30623807
|
C | T | 15 | a0001c0001t0002g0160a0003c0003t0004g0198a0003c0003t0004g0199others(12): Show | 16 | HG00609.hp2 HG00733.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1222+724C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623807 | ||||||
chr22:30623809
|
T | C | 10 | a0002c0002t0001g0062a0002c0002t0001g0151a0002c0002t0001g0152others(7): Show | 12 | HG01346.hp1 HG01884.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1222+726T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623809 | ||||||
chr22:30623811
|
T | C | 9 | a0003c0003t0004g0198a0003c0003t0004g0199a0003c0003t0004g0200others(6): Show | 9 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+728T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623811 | ||||||
chr22:30623813
|
T | C | 27 | a0001c0001t0001g0019a0001c0001t0002g0161a0001c0001t0021g0156others(24): Show | 30 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1222+730T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623813 | ||||||
chr22:30623813
|
TACACACA others(1): Show |
T | 3 | a0007c0007t0007g0009a0007c0007t0007g0078a0007c0007t0007g0080 | 6 | HG01261.hp1 HG02647.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+732_1222+739d others(10): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623813 | |||||
chr22:30623815
|
C | T | 72 | a0001c0001t0001g0231a0001c0001t0002g0002a0001c0001t0002g0006others(69): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1222+732C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623815 | ||||||
chr22:30623817
|
C | T | 10 | a0001c0001t0001g0019a0003c0003t0004g0198a0003c0003t0004g0199others(7): Show | 11 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+734C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623817 | ||||||
chr22:30623819
|
C | CAT | 3 | a0001c0001t0002g0030a0001c0001t0002g0172a0005c0005t0002g0067 | 4 | HG00423.hp2 HG01192.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+737_1222+738i others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623819 | |||||
chr22:30623819
|
C | T | 31 | a0001c0001t0001g0019a0001c0001t0002g0161a0001c0001t0003g0325others(28): Show | 34 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1222+736C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623819 | ||||||
chr22:30623821
|
C | CAT | 8 | a0006c0006t0001g0043a0006c0006t0001g0063a0006c0006t0001g0223others(5): Show | 9 | HG02109.hp1 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+740_1222+741d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | |||||
chr22:30623821
|
C | CATACATA others(77): Show |
1 | a0001c0001t0003g0328 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1222+743_1222+744i others(86): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | |||||
chr22:30623821
|
C | CATACATA others(69): Show |
4 | a0001c0001t0003g0316a0001c0001t0003g0329a0001c0001t0003g0331others(1): Show | 4 | HG04115.hp2 NA18957.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+743_1222+744i others(78): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | |||||
chr22:30623821
|
C | CATACATA others(81): Show |
22 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(19): Show | 24 | HG00642.hp1 HG00733.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1222+743_1222+744i others(90): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | |||||
chr22:30623821
|
C | CATACATA others(83): Show |
2 | a0001c0001t0010g0103a0001c0001t0010g0104 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1222+743_1222+744i others(92): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | |||||
chr22:30623821
|
C | CATAT | 70 | a0001c0001t0001g0231a0001c0001t0002g0002a0001c0001t0002g0006others(67): Show | 98 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1222+741_1222+742i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | |||||
chr22:30623821
|
C | CATATATA others(65): Show |
1 | a0001c0001t0003g0325 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1222+741_1222+742i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | |||||
chr22:30623821
|
C | T | 59 | a0001c0001t0001g0019a0001c0001t0002g0030a0001c0001t0002g0160others(56): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.1222+738C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623821 | ||||||
chr22:30623823
|
TAC | T | 19 | a0002c0002t0001g0005a0002c0002t0001g0017a0002c0002t0001g0029others(16): Show | 23 | HG00597.hp2 HG00738.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.1222+748_1222+749d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623823 | |||||
chr22:30623825
|
C | CATATATA others(67): Show |
3 | a0001c0001t0008g0343a0001c0001t0008g0344a0001c0001t0008g0345 | 3 | HG02280.hp2 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1222+743_1222+744i others(76): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | |||||
chr22:30623825
|
C | CATATATA others(103): Show |
1 | a0001c0001t0003g0321 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1222+743_1222+744i others(112): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | |||||
chr22:30623825
|
C | CATATATA others(107): Show |
9 | a0001c0001t0006g0016a0001c0001t0006g0020a0001c0001t0006g0021others(6): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1222+743_1222+744i others(116): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | |||||
chr22:30623825
|
C | CATATATA others(69): Show |
2 | a0001c0001t0003g0090a0001c0001t0003g0095 | 2 | HG00558.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1222+743_1222+744i others(78): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | |||||
chr22:30623825
|
C | CATATATA others(79): Show |
2 | a0001c0001t0003g0087a0009c0009t0003g0026 | 3 | HG01257.hp2 HG01258.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1222+743_1222+744i others(88): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | |||||
chr22:30623825
|
C | CATATATA others(81): Show |
27 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(24): Show | 36 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1222+743_1222+744i others(90): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | |||||
chr22:30623825
|
C | T | 43 | a0001c0001t0001g0231a0001c0001t0002g0030a0001c0001t0002g0033others(40): Show | 50 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1222+742C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623825 | ||||||
chr22:30623826
|
A | G | 3 | a0003c0003t0004g0202a0003c0003t0004g0203a0007c0007t0004g0121 | 3 | HG01884.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1222+743A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623826 | ||||||
chr22:30623827
|
C | T | 10 | a0001c0001t0002g0033a0001c0001t0002g0171a0003c0003t0004g0202others(7): Show | 12 | HG00639.hp1 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+744C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623827 | ||||||
chr22:30623829
|
C | T | 6 | a0003c0003t0004g0202a0003c0003t0004g0203a0005c0005t0011g0354others(3): Show | 6 | HG00099.hp2 HG01106.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+746C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623829 | ||||||
chr22:30623829
|
CACA | C | 2 | a0001c0001t0002g0033a0001c0001t0002g0171 | 3 | HG00639.hp1 HG02148.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1222+747_1222+749d others(5): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623829 | ||||||
chr22:30623831
|
C | T | 132 | a0001c0001t0001g0019a0001c0001t0002g0002a0001c0001t0002g0006others(129): Show | 172 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1222+748C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623831 | ||||||
chr22:30623833
|
T | C | 4 | a0006c0006t0001g0043a0006c0006t0001g0063a0006c0006t0001g0223others(1): Show | 5 | HG02109.hp1 HG02486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+750T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623833 | ||||||
chr22:30623833
|
T | TAC | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+751_1222+752i others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623833 | |||||
chr22:30623835
|
TAC | T | 8 | a0001c0001t0006g0016a0001c0001t0006g0020a0001c0001t0006g0021others(5): Show | 12 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+760_1222+761d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623835 | |||||
chr22:30623837
|
C | T | 160 | a0001c0001t0001g0089a0001c0001t0001g0231a0001c0001t0002g0002others(157): Show | 204 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1222+754C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623837 | ||||||
chr22:30623839
|
C | T | 6 | a0001c0001t0001g0231a0001c0001t0002g0160a0001c0014t0001g0229others(3): Show | 6 | HG00609.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+756C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623839 | ||||||
chr22:30623842
|
A | ATGCACAC others(35): Show |
1 | a0001c0001t0008g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1222+759_1222+760i others(44): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623842 | ||||||
chr22:30623843
|
C | CATAT | 4 | a0005c0005t0001g0038a0005c0005t0001g0074a0005c0005t0001g0192others(1): Show | 5 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+763_1222+764i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623843 | |||||
chr22:30623843
|
C | T | 37 | a0001c0001t0001g0019a0001c0001t0002g0030a0001c0001t0002g0033others(34): Show | 51 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1222+760C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623843 | ||||||
chr22:30623845
|
T | C | 4 | a0001c0001t0002g0160a0005c0011t0001g0022a0005c0011t0001g0071others(1): Show | 5 | HG00609.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+762T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623845 | ||||||
chr22:30623845
|
TAC | T | 2 | a0001c0001t0003g0010a0001c0001t0003g0082 | 5 | NA18947.hp1 NA18971.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+764_1222+765d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623845 | |||||
chr22:30623847
|
C | T | 172 | a0001c0001t0001g0089a0001c0001t0001g0231a0001c0001t0002g0002others(169): Show | 213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1222+764C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623847 | ||||||
chr22:30623847
|
CAT | C | 6 | a0001c0001t0002g0033a0001c0001t0002g0171a0001c0001t0003g0088others(3): Show | 7 | HG00323.hp1 HG00639.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+766_1222+767d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623847 | |||||
chr22:30623848
|
A | G | 2 | a0003c0003t0004g0205a0007c0007t0004g0121 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1222+765A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623848 | ||||||
chr22:30623849
|
T | C | 126 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0002g0002others(123): Show | 166 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1222+766T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623849 | ||||||
chr22:30623849
|
TACAC | T | 4 | a0002c0002t0001g0291a0005c0011t0001g0022a0005c0011t0001g0071others(1): Show | 5 | HG02056.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+768_1222+771d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623849 | |||||
chr22:30623851
|
C | CACACATA others(3): Show |
1 | a0005c0005t0001g0195 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1222+771_1222+772i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623851 | |||||
chr22:30623851
|
C | T | 11 | a0001c0001t0008g0343a0001c0001t0008g0344a0001c0001t0008g0345others(8): Show | 15 | HG01261.hp1 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1222+768C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623851 | ||||||
chr22:30623853
|
C | CACAT | 3 | a0005c0005t0002g0064a0005c0005t0002g0068a0005c0005t0015g0065 | 3 | HG02109.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+771_1222+772i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623853 | |||||
chr22:30623853
|
C | T | 17 | a0003c0003t0004g0202a0003c0003t0004g0203a0004c0004t0001g0124others(14): Show | 27 | HG01243.hp2 HG01496.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1222+770C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623853 | ||||||
chr22:30623855
|
T | C | 28 | a0001c0001t0001g0231a0001c0001t0002g0030a0001c0001t0002g0160others(25): Show | 36 | HG00423.hp2 HG00609.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.1222+772T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623855 | ||||||
chr22:30623857
|
C | CATACACA others(5): Show |
1 | a0002c0002t0001g0301 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1222+802_1222+813d others(14): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623857 | |||||
chr22:30623857
|
C | T | 198 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(195): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1222+774C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623857 | ||||||
chr22:30623859
|
T | C | 7 | a0003c0003t0004g0202a0003c0003t0004g0203a0004c0004t0007g0125others(4): Show | 8 | HG01884.hp2 HG02683.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+776T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623859 | ||||||
chr22:30623859
|
T | TACATAC | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+779_1222+780i others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623859 | |||||
chr22:30623859
|
TAC | T | 3 | a0007c0007t0007g0009a0007c0007t0007g0078a0007c0007t0007g0080 | 6 | HG01261.hp1 HG02647.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+782_1222+783d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623859 | |||||
chr22:30623860
|
A | G | 1 | a0001c0001t0001g0019 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1222+777A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623860 | ||||||
chr22:30623861
|
C | T | 69 | a0001c0001t0001g0019a0001c0001t0001g0231a0001c0001t0002g0002others(66): Show | 98 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1222+778C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623861 | ||||||
chr22:30623863
|
C | T | 4 | a0001c0001t0001g0019a0003c0003t0004g0040a0003c0003t0007g0220others(1): Show | 6 | HG01496.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+780C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623863 | ||||||
chr22:30623865
|
C | T | 5 | a0004c0004t0007g0125a0005c0005t0001g0194a0005c0011t0001g0022others(2): Show | 6 | HG02683.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+782C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623865 | ||||||
chr22:30623867
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 86 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1222+784T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623867 | ||||||
chr22:30623870
|
A | G | 1 | a0003c0003t0004g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1222+787A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623870 | ||||||
chr22:30623871
|
T | C | 6 | a0001c0001t0001g0019a0001c0001t0021g0156a0004c0004t0007g0125others(3): Show | 8 | HG01496.hp2 HG01981.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+788T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623871 | ||||||
chr22:30623871
|
TAC | T | 29 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(26): Show | 31 | HG00642.hp1 HG00733.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1222+794_1222+795d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623871 | |||||
chr22:30623872
|
A | G | 19 | a0003c0003t0004g0202a0003c0003t0004g0203a0003c0003t0004g0204others(16): Show | 29 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1222+789A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623872 | ||||||
chr22:30623873
|
C | T | 24 | a0001c0001t0002g0160a0001c0001t0008g0343a0001c0001t0008g0344others(21): Show | 35 | HG00609.hp2 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1222+790C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623873 | ||||||
chr22:30623875
|
C | CACACATA others(5): Show |
1 | a0007c0007t0004g0121 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1222+795_1222+796i others(14): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | |||||
chr22:30623875
|
C | CACACATA others(221): Show |
1 | a0003c0003t0007g0220 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1222+795_1222+796i others(230): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | |||||
chr22:30623875
|
C | CACACATA others(197): Show |
1 | a0003c0003t0012g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1222+795_1222+796i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | |||||
chr22:30623875
|
C | CACATATA others(65): Show |
1 | a0001c0001t0002g0176 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1222+812_1222+813i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | |||||
chr22:30623875
|
C | CACATATA others(53): Show |
2 | a0001c0001t0002g0030a0001c0001t0002g0172 | 3 | HG00423.hp2 NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1222+800_1222+801i others(62): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | |||||
chr22:30623875
|
C | CATATATA others(249): Show |
1 | a0001c0001t0003g0316 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1222+793_1222+794i others(258): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | |||||
chr22:30623875
|
C | CATATGTA others(175): Show |
1 | a0003c0003t0004g0040 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1222+793_1222+794i others(184): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | |||||
chr22:30623875
|
C | T | 46 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230others(43): Show | 58 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1222+792C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623875 | ||||||
chr22:30623877
|
C | CACATATA others(107): Show |
1 | a0001c0001t0001g0019 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1222+795_1222+796i others(116): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623877 | |||||
chr22:30623877
|
C | CAT | 3 | a0005c0005t0002g0064a0005c0005t0002g0068a0005c0005t0015g0065 | 3 | HG02109.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+800_1222+801d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623877 | |||||
chr22:30623877
|
C | T | 7 | a0001c0001t0002g0313a0001c0001t0021g0156a0005c0011t0001g0022others(4): Show | 8 | HG00099.hp2 HG01106.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+794C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623877 | ||||||
chr22:30623877
|
CAT | C | 2 | a0002c0010t0001g0012a0002c0010t0001g0233 | 5 | HG00741.hp2 HG01069.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+800_1222+801d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623877 | |||||
chr22:30623877
|
CATATATA others(21): Show |
C | 1 | a0002c0002t0001g0240 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1222+828_1222+855d others(30): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623877 | |||||
chr22:30623879
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0002g0160a0005c0005t0001g0039 | 5 | HG00609.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+796T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623879 | ||||||
chr22:30623879
|
T | TATACAC | 4 | a0005c0005t0001g0038a0005c0005t0001g0192a0005c0005t0001g0194others(1): Show | 5 | HG02622.hp1 HG02717.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+799_1222+800i others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623879 | |||||
chr22:30623879
|
T | TATATATA others(61): Show |
1 | a0005c0005t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1222+801_1222+802i others(70): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623879 | |||||
chr22:30623879
|
T | TATATGTA others(3): Show |
3 | a0005c0005t0001g0037a0005c0005t0001g0193a0005c0005t0001g0195 | 4 | HG01099.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+800_1222+801i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623879 | |||||
chr22:30623880
|
A | G | 13 | a0003c0003t0004g0041a0003c0003t0004g0042a0003c0003t0004g0197others(10): Show | 15 | HG00140.hp1 HG00280.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1222+797A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623880 | ||||||
chr22:30623885
|
C | T | 8 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0192others(5): Show | 10 | HG01099.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1222+802C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623885 | ||||||
chr22:30623885
|
CACACATA others(7): Show |
C | 1 | a0007c0007t0007g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1222+804_1222+817d others(16): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623885 | |||||
chr22:30623885
|
CACACATA others(61): Show |
C | 1 | a0007c0007t0007g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1222+804_1222+871d others(70): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623885 | |||||
chr22:30623887
|
CACAT | C | 3 | a0007c0007t0007g0009a0007c0007t0007g0078a0007c0007t0007g0080 | 6 | HG01261.hp1 HG02647.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+806_1222+809d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623887 | |||||
chr22:30623889
|
CAT | C | 84 | a0001c0001t0001g0231a0001c0001t0002g0002a0001c0001t0002g0006others(81): Show | 117 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1222+813_1222+814d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623889 | |||||
chr22:30623891
|
T | C | 31 | a0001c0001t0001g0019a0001c0001t0003g0325a0001c0001t0003g0329others(28): Show | 37 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1222+808T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623891 | ||||||
chr22:30623891
|
T | TATATACA others(193): Show |
1 | a0005c0005t0015g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1222+813_1222+814i others(202): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623891 | |||||
chr22:30623891
|
T | TATATACA others(215): Show |
1 | a0005c0005t0002g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1222+813_1222+814i others(224): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623891 | |||||
chr22:30623891
|
T | TATATGTA others(167): Show |
1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+812_1222+813i others(176): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623891 | |||||
chr22:30623893
|
T | C | 16 | a0001c0001t0001g0231a0001c0001t0003g0316a0001c0014t0001g0229others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1222+810T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623893 | ||||||
chr22:30623893
|
T | TATACACA others(135): Show |
1 | a0005c0005t0002g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1222+813_1222+814i others(144): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | |||||
chr22:30623893
|
T | TATATACA others(149): Show |
1 | a0005c0005t0002g0066 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1222+814_1222+815i others(158): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | |||||
chr22:30623893
|
T | TATGTATA others(237): Show |
1 | a0003c0003t0004g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1222+812_1222+813i others(246): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | |||||
chr22:30623893
|
T | TATGTATA others(133): Show |
1 | a0003c0003t0004g0197 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1222+812_1222+813i others(142): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | |||||
chr22:30623893
|
T | TATGTATA others(131): Show |
6 | a0003c0003t0004g0041a0003c0003t0004g0206a0003c0003t0004g0213others(3): Show | 7 | HG01358.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+812_1222+813i others(140): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | |||||
chr22:30623893
|
T | TATGTATA others(129): Show |
3 | a0003c0003t0004g0042a0003c0003t0004g0207a0003c0003t0004g0218 | 4 | HG01978.hp1 HG01993.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+812_1222+813i others(138): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | |||||
chr22:30623893
|
T | TATGTATA others(127): Show |
1 | a0003c0003t0004g0224 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1222+812_1222+813i others(136): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | |||||
chr22:30623897
|
T | TACACAC | 2 | a0005c0011t0001g0022a0005c0011t0001g0077 | 3 | HG02896.hp2 HG02897.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1222+814_1222+815i others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623897 | ||||||
chr22:30623898
|
G | A | 10 | a0001c0001t0002g0160a0001c0001t0002g0187a0005c0011t0001g0022others(7): Show | 14 | HG00099.hp2 HG00609.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1222+815G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623898 | ||||||
chr22:30623899
|
T | C | 8 | a0005c0005t0002g0067a0005c0005t0011g0354a0005c0011t0001g0071others(5): Show | 11 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+816T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623899 | ||||||
chr22:30623901
|
T | C | 6 | a0001c0001t0021g0156a0005c0005t0002g0067a0005c0005t0011g0354others(3): Show | 6 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+818T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623901 | ||||||
chr22:30623902
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1222+819A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623902 | ||||||
chr22:30623903
|
C | CACACATA others(5): Show |
1 | a0001c0001t0002g0187 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1222+821_1222+822i others(14): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623903 | |||||
chr22:30623903
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1222+820C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623903 | ||||||
chr22:30623903
|
CAT | C | 30 | a0001c0001t0002g0176a0003c0003t0004g0041a0003c0003t0004g0042others(27): Show | 41 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.1222+828_1222+829d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623903 | |||||
chr22:30623905
|
T | C | 4 | a0001c0001t0021g0156a0005c0005t0002g0067a0005c0011t0001g0022others(1): Show | 5 | HG01192.hp2 HG01981.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+822T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623905 | ||||||
chr22:30623905
|
T | TATATACA others(19): Show |
1 | a0002c0002t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1222+827_1222+828i others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623905 | |||||
chr22:30623905
|
T | TATATACA others(17): Show |
2 | a0002c0002t0001g0287a0002c0002t0001g0293 | 2 | HG00673.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1222+827_1222+828i others(26): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623905 | |||||
chr22:30623905
|
T | TATATACA others(195): Show |
1 | a0001c0001t0003g0318 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1222+827_1222+828i others(204): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623905 | |||||
chr22:30623905
|
T | TATATACA others(87): Show |
3 | a0004c0004t0002g0028a0004c0004t0005g0112a0004c0004t0005g0118 | 4 | HG01884.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+827_1222+828i others(96): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623905 | |||||
chr22:30623905
|
T | TATATATA others(19): Show |
4 | a0006c0006t0001g0061a0006c0006t0001g0347a0006c0006t0001g0348others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+836_1222+861d others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623905 | |||||
chr22:30623907
|
T | C | 2 | a0001c0001t0002g0160a0001c0001t0002g0187 | 2 | HG00609.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1222+824T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623907 | ||||||
chr22:30623907
|
T | TATACACA others(13): Show |
1 | a0005c0005t0001g0038 | 2 | HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1222+827_1222+828i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623907 | |||||
chr22:30623907
|
T | TATACACA others(37): Show |
1 | a0005c0005t0001g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1222+827_1222+828i others(46): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623907 | |||||
chr22:30623909
|
T | C | 4 | a0005c0005t0011g0354a0005c0011t0001g0071a0013c0013t0011g0190others(1): Show | 4 | HG00099.hp2 HG01106.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+826T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623909 | ||||||
chr22:30623909
|
TATAC | T | 61 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 87 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1222+828_1222+831d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623909 | |||||
chr22:30623911
|
T | C | 29 | a0001c0001t0001g0231a0001c0001t0002g0030a0001c0001t0002g0172others(26): Show | 34 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.1222+828T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623911 | ||||||
chr22:30623913
|
C | T | 8 | a0001c0001t0002g0160a0001c0001t0002g0187a0005c0005t0001g0038others(5): Show | 9 | HG00099.hp2 HG00609.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+830C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623913 | ||||||
chr22:30623915
|
C | T | 4 | a0005c0005t0011g0354a0005c0011t0001g0071a0013c0013t0011g0190others(1): Show | 4 | HG00099.hp2 HG01106.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+832C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623915 | ||||||
chr22:30623915
|
CACATAT | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0172 | 3 | HG00423.hp2 NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1222+834_1222+839d others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623915 | |||||
chr22:30623917
|
C | T | 1 | a0005c0005t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+834C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623917 | ||||||
chr22:30623917
|
CAT | C | 9 | a0001c0001t0021g0156a0002c0002t0001g0263a0002c0002t0001g0268others(6): Show | 9 | HG00642.hp2 HG01069.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+841_1222+842d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623917 | |||||
chr22:30623917
|
CATAT | C | 7 | a0001c0001t0001g0231a0005c0011t0001g0022a0005c0011t0001g0077others(4): Show | 11 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1222+839_1222+842d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623917 | |||||
chr22:30623919
|
T | C | 90 | a0001c0001t0001g0019a0001c0001t0002g0002a0001c0001t0002g0006others(87): Show | 120 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1222+836T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623919 | ||||||
chr22:30623919
|
T | TATATATG others(19): Show |
30 | a0002c0002t0001g0005a0002c0002t0001g0017a0002c0002t0001g0029others(27): Show | 35 | HG00597.hp2 HG00735.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1222+838_1222+863d others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623919 | |||||
chr22:30623919
|
T | TATATATG others(45): Show |
1 | a0002c0002t0019g0144 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1222+863_1222+864i others(54): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623919 | |||||
chr22:30623919
|
T | TATATATG others(43): Show |
1 | a0002c0002t0001g0280 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1222+861_1222+862i others(52): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623919 | |||||
chr22:30623919
|
T | TATATGTA others(17): Show |
4 | a0002c0002t0001g0282a0002c0002t0001g0290a0002c0002t0009g0045others(1): Show | 5 | HG01168.hp2 HG01169.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+840_1222+841i others(26): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623919 | |||||
chr22:30623921
|
T | C | 6 | a0001c0001t0003g0316a0001c0001t0003g0318a0005c0005t0011g0354others(3): Show | 6 | HG00099.hp2 HG01106.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+838T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TACACACA others(189): Show |
1 | a0001c0001t0003g0097 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1222+839_1222+840i others(198): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(197): Show |
1 | a0001c0001t0003g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(195): Show |
1 | a0001c0001t0003g0336 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(204): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(197): Show |
1 | a0001c0001t0003g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(201): Show |
18 | a0001c0001t0003g0011a0001c0001t0003g0023a0001c0001t0003g0024others(15): Show | 24 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(210): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(251): Show |
1 | a0001c0001t0003g0088 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(260): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(199): Show |
1 | a0001c0001t0003g0326 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(208): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(199): Show |
19 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0096others(16): Show | 20 | HG00642.hp1 HG01168.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(208): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(225): Show |
1 | a0001c0001t0003g0332 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(234): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(199): Show |
2 | a0001c0001t0003g0010a0001c0001t0003g0082 | 5 | NA18947.hp1 NA18971.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(208): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(199): Show |
1 | a0001c0001t0003g0340 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(208): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(197): Show |
4 | a0001c0001t0003g0060a0001c0001t0003g0319a0001c0001t0003g0338others(1): Show | 5 | HG01981.hp1 HG02273.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(195): Show |
1 | a0001c0001t0003g0342 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(204): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(197): Show |
1 | a0001c0001t0001g0089 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(195): Show |
1 | a0001c0001t0003g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(204): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(197): Show |
1 | a0001c0001t0003g0327 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(197): Show |
1 | a0001c0001t0003g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(195): Show |
2 | a0001c0001t0010g0103a0001c0001t0010g0104 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1222+841_1222+842i others(204): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(259): Show |
1 | a0001c0001t0006g0070 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(268): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(153): Show |
1 | a0001c0001t0006g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(162): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(125): Show |
4 | a0001c0001t0006g0016a0001c0001t0006g0020a0001c0001t0006g0072others(1): Show | 7 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(134): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(151): Show |
1 | a0001c0001t0006g0069 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(160): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATACACA others(151): Show |
1 | a0001c0001t0006g0021 | 2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1222+841_1222+842i others(160): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TATGCACA others(201): Show |
1 | a0001c0001t0003g0087 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1222+840_1222+841i others(210): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | |||||
chr22:30623921
|
T | TGTATACA others(325): Show |
1 | a0003c0003t0004g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(334): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(303): Show |
1 | a0003c0025t0012g0212 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(312): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(303): Show |
1 | a0003c0003t0004g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(312): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(301): Show |
1 | a0003c0003t0004g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(310): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(301): Show |
1 | a0003c0003t0004g0221 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(310): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(57): Show |
1 | a0003c0003t0012g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(66): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(81): Show |
1 | a0003c0003t0007g0220 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(90): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(37): Show |
1 | a0003c0003t0004g0040 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1222+838_1222+839i others(46): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(87): Show |
1 | a0003c0003t0004g0201 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(96): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(113): Show |
2 | a0003c0003t0004g0199a0003c0003t0004g0200 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1222+838_1222+839i others(122): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(285): Show |
1 | a0003c0003t0004g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(294): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(33): Show |
1 | a0003c0003t0004g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(42): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(35): Show |
1 | a0003c0003t0004g0219 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(44): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(57): Show |
1 | a0003c0003t0004g0214 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(66): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623921
|
T | TGTATACA others(229): Show |
2 | a0001c0014t0001g0229a0001c0014t0001g0230 | 2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1222+838_1222+839i others(238): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | ||||||
chr22:30623923
|
T | C | 3 | a0001c0014t0001g0229a0001c0014t0001g0230a0005c0005t0002g0067 | 3 | HG01192.hp2 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1222+840T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623923 | ||||||
chr22:30623923
|
T | TACACACA others(171): Show |
4 | a0009c0009t0003g0026a0009c0009t0003g0102a0009c0009t0003g0106others(1): Show | 5 | HG00323.hp1 HG01175.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(180): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623923 | |||||
chr22:30623923
|
T | TACACACA others(171): Show |
1 | a0001c0001t0003g0339 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(180): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623923 | |||||
chr22:30623925
|
T | C | 1 | a0005c0005t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+842T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623925 | ||||||
chr22:30623926
|
G | A | 1 | a0005c0005t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+843G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623926 | ||||||
chr22:30623927
|
T | C | 1 | a0005c0005t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+844T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623927 | ||||||
chr22:30623931
|
C | T | 1 | a0005c0005t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+848C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623931 | ||||||
chr22:30623933
|
T | C | 1 | a0005c0005t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+850T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623933 | ||||||
chr22:30623933
|
T | TATATACA others(17): Show |
1 | a0002c0002t0001g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1222+863_1222+864i others(26): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623933 | |||||
chr22:30623935
|
T | C | 1 | a0005c0005t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+852T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623935 | ||||||
chr22:30623937
|
TAC | T | 79 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(76): Show | 107 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1222+864_1222+865d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623937 | |||||
chr22:30623937
|
TACAC | T | 4 | a0001c0001t0021g0156a0004c0004t0002g0028a0004c0004t0005g0112others(1): Show | 5 | HG01884.hp1 HG01981.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+862_1222+865d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623937 | |||||
chr22:30623939
|
C | CACACATA others(69): Show |
3 | a0005c0011t0001g0022a0005c0011t0001g0071a0005c0011t0001g0077 | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+861_1222+862i others(78): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623939 | |||||
chr22:30623939
|
C | T | 10 | a0001c0001t0001g0231a0001c0001t0006g0075a0004c0004t0007g0125others(7): Show | 12 | HG00639.hp2 HG01099.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+856C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623939 | ||||||
chr22:30623941
|
C | CACATATA others(111): Show |
8 | a0004c0004t0001g0124a0004c0004t0005g0001a0004c0004t0005g0110others(5): Show | 17 | HG01243.hp2 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1222+861_1222+862i others(120): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623941 | |||||
chr22:30623941
|
C | CACATATA others(109): Show |
1 | a0020c0017t0022g0320 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1222+861_1222+862i others(118): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623941 | |||||
chr22:30623941
|
C | CACATATA others(63): Show |
1 | a0005c0005t0001g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1222+861_1222+862i others(72): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623941 | |||||
chr22:30623941
|
C | CATATATA others(11): Show |
1 | a0005c0005t0015g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1222+859_1222+860i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623941 | |||||
chr22:30623941
|
C | T | 2 | a0001c0001t0002g0170a0005c0005t0002g0067 | 2 | HG01192.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1222+858C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623941 | ||||||
chr22:30623943
|
C | CACATATA others(73): Show |
1 | a0001c0001t0006g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1222+863_1222+864i others(82): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623943 | |||||
chr22:30623943
|
C | T | 1 | a0005c0005t0015g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1222+860C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623943 | ||||||
chr22:30623945
|
C | CATATATA others(23): Show |
1 | a0010c0012t0020g0228 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1222+863_1222+864i others(32): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623945 | |||||
chr22:30623945
|
C | T | 81 | a0001c0001t0001g0089a0001c0001t0002g0030a0001c0001t0002g0160others(78): Show | 98 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1222+862C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623945 | ||||||
chr22:30623947
|
C | T | 173 | a0001c0001t0001g0019a0001c0001t0002g0002a0001c0001t0002g0006others(170): Show | 224 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1222+864C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623947 | ||||||
chr22:30623949
|
T | C | 1 | a0001c0001t0006g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1222+866T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623949 | ||||||
chr22:30623956
|
A | G | 1 | a0001c0001t0002g0176 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1222+873A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623956 | ||||||
chr22:30623957
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1222+874C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623957 | ||||||
chr22:30623963
|
TAC | T | 68 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(65): Show | 97 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1222+888_1222+889d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623963 | |||||
chr22:30623965
|
C | CACACACA others(45): Show |
24 | a0002c0002t0001g0004a0002c0002t0001g0051a0002c0002t0001g0052others(21): Show | 33 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1222+889_1222+890i others(54): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | |||||
chr22:30623965
|
C | CACACACA others(71): Show |
2 | a0002c0002t0001g0289a0002c0002t0009g0242 | 2 | HG00741.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1222+889_1222+890i others(80): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | |||||
chr22:30623965
|
C | CACACACA others(15): Show |
1 | a0002c0002t0001g0279 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1222+889_1222+890i others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | |||||
chr22:30623965
|
C | CACACACA others(43): Show |
5 | a0002c0002t0001g0015a0002c0002t0001g0238a0002c0002t0001g0295others(2): Show | 7 | HG00140.hp2 HG01109.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+889_1222+890i others(52): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | |||||
chr22:30623965
|
C | CACACACA others(41): Show |
1 | a0002c0002t0017g0298 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1222+889_1222+890i others(50): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | |||||
chr22:30623965
|
C | CACACACA others(45): Show |
1 | a0002c0002t0001g0239 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1222+907_1222+908i others(54): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | |||||
chr22:30623965
|
C | CACACACA others(19): Show |
11 | a0002c0002t0001g0050a0002c0002t0001g0280a0002c0002t0001g0282others(8): Show | 16 | HG00423.hp1 HG00673.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1222+942_1222+967d others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | |||||
chr22:30623965
|
C | CACACACA others(45): Show |
1 | a0002c0002t0001g0305 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1222+916_1222+967d others(54): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | |||||
chr22:30623965
|
C | CACACACA others(71): Show |
2 | a0002c0002t0001g0055a0002c0002t0001g0244 | 3 | NA18940.hp2 NA18956.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1222+894_1222+895i others(80): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | |||||
chr22:30623965
|
C | T | 91 | a0001c0001t0001g0089a0001c0001t0001g0231a0001c0001t0002g0176others(88): Show | 116 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.1222+882C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623965 | ||||||
chr22:30623965
|
CACACACA others(19): Show |
C | 2 | a0002c0002t0001g0247a0002c0002t0001g0255 | 2 | HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1222+942_1222+967d others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | |||||
chr22:30623967
|
C | CACACACA others(43): Show |
1 | a0002c0002t0001g0286 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1222+889_1222+890i others(52): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623967 | |||||
chr22:30623967
|
C | CACATATA others(37): Show |
1 | a0005c0005t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+887_1222+888i others(46): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623967 | |||||
chr22:30623967
|
C | CATATATG others(3): Show |
1 | a0001c0001t0002g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1222+885_1222+886i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623967 | |||||
chr22:30623969
|
CACAT | C | 9 | a0001c0001t0002g0030a0001c0001t0002g0127a0001c0001t0002g0171others(6): Show | 12 | HG00423.hp2 HG00639.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+888_1222+891d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623969 | |||||
chr22:30623971
|
C | T | 2 | a0001c0001t0002g0175a0005c0005t0001g0193 | 2 | HG02922.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1222+888C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623971 | ||||||
chr22:30623971
|
CAT | C | 21 | a0001c0001t0001g0019a0001c0001t0002g0176a0002c0002t0001g0148others(18): Show | 24 | HG00099.hp2 HG00733.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1222+895_1222+896d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623971 | |||||
chr22:30623971
|
CATAT | C | 9 | a0001c0014t0001g0229a0001c0014t0001g0230a0003c0003t0004g0214others(6): Show | 12 | HG00140.hp1 HG01261.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+893_1222+896d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623971 | |||||
chr22:30623973
|
T | C | 4 | a0001c0001t0001g0231a0002c0002t0001g0286a0003c0003t0004g0201others(1): Show | 4 | HG01192.hp2 HG02895.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+890T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623973 | ||||||
chr22:30623973
|
T | TATATGTA others(17): Show |
1 | a0006c0006t0001g0063 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1222+894_1222+895i others(26): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623973 | |||||
chr22:30623973
|
T | TATGTATA others(205): Show |
1 | a0003c0003t0004g0219 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1222+892_1222+893i others(214): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623973 | |||||
chr22:30623975
|
T | C | 69 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(66): Show | 85 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1222+892T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623975 | ||||||
chr22:30623975
|
T | TATGTATA others(111): Show |
2 | a0003c0003t0004g0199a0003c0003t0004g0200 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1222+894_1222+895i others(120): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623975 | |||||
chr22:30623975
|
T | TATGTATA others(35): Show |
1 | a0005c0005t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1222+894_1222+895i others(44): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623975 | |||||
chr22:30623975
|
T | TGTATACA others(103): Show |
1 | a0003c0003t0004g0213 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1222+892_1222+893i others(112): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623975 | ||||||
chr22:30623975
|
T | TGTATACA others(77): Show |
10 | a0003c0003t0004g0041a0003c0003t0004g0042a0003c0003t0004g0197others(7): Show | 12 | HG01256.hp1 HG01515.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.1222+892_1222+893i others(86): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623975 | ||||||
chr22:30623975
|
T | TGTATACA others(11): Show |
1 | a0005c0005t0001g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1222+892_1222+893i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623975 | ||||||
chr22:30623975
|
T | TGTATACA others(181): Show |
1 | a0003c0003t0004g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1222+892_1222+893i others(190): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623975 | ||||||
chr22:30623977
|
T | TGTATACA others(91): Show |
1 | a0001c0001t0001g0231 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1222+894_1222+895i others(100): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623977 | ||||||
chr22:30623984
|
A | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0172 | 3 | HG00423.hp2 NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1222+901A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623984 | ||||||
chr22:30623985
|
C | CAT | 45 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(42): Show | 48 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1222+908_1222+909d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623985 | |||||
chr22:30623985
|
C | CATATATA others(51): Show |
1 | a0010c0012t0001g0226 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1222+915_1222+916i others(60): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623985 | |||||
chr22:30623985
|
C | CATATATA others(39): Show |
2 | a0005c0005t0002g0066a0005c0005t0002g0068 | 2 | HG00642.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+909_1222+910i others(48): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623985 | |||||
chr22:30623991
|
T | C | 4 | a0001c0001t0002g0035a0001c0001t0002g0180a0001c0001t0002g0181others(1): Show | 5 | NA18962.hp1 NA18995.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+908T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623991 | ||||||
chr22:30623991
|
T | TAC | 7 | a0001c0001t0006g0070a0002c0002t0001g0148a0002c0002t0001g0240others(4): Show | 8 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+914_1222+915d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623991 | |||||
chr22:30623993
|
C | CACACACA others(49): Show |
1 | a0010c0012t0001g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1222+915_1222+916i others(58): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623993 | |||||
chr22:30623993
|
C | T | 6 | a0001c0001t0002g0030a0001c0001t0002g0172a0001c0001t0002g0176others(3): Show | 8 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222+910C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623993 | ||||||
chr22:30623995
|
CACATAT | C | 4 | a0001c0001t0002g0035a0001c0001t0002g0180a0001c0001t0002g0181others(1): Show | 5 | NA18962.hp1 NA18995.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+914_1222+919d others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623995 | |||||
chr22:30623997
|
CAT | C | 7 | a0001c0014t0001g0229a0001c0014t0001g0230a0003c0003t0004g0040others(4): Show | 9 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+921_1222+922d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623997 | |||||
chr22:30623997
|
CATAT | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(43): Show | 68 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1222+919_1222+922d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623997 | |||||
chr22:30623997
|
CATATAT | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0108a0001c0001t0002g0109 | 4 | HG01070.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+917_1222+922d others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623997 | |||||
chr22:30623999
|
T | C | 46 | a0001c0001t0001g0019a0001c0001t0001g0231a0001c0001t0002g0030others(43): Show | 54 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1222+916T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623999 | ||||||
chr22:30623999
|
T | TATGTATA others(65): Show |
1 | a0001c0001t0002g0312 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1222+918_1222+919i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623999 | |||||
chr22:30624001
|
T | C | 18 | a0001c0001t0003g0323a0001c0001t0003g0331a0001c0001t0003g0332others(15): Show | 22 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1222+918T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624001 | ||||||
chr22:30624001
|
T | TATGTATA others(9): Show |
1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1222+920_1222+921i others(18): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624001 | |||||
chr22:30624001
|
T | TATGTATA others(13): Show |
4 | a0004c0004t0005g0114a0004c0004t0005g0115a0004c0004t0005g0123others(1): Show | 4 | HG01106.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+920_1222+921i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624001 | |||||
chr22:30624001
|
T | TATGTATA others(83): Show |
1 | a0013c0013t0011g0190 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1222+920_1222+921i others(92): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624001 | |||||
chr22:30624001
|
T | TGTATACA others(11): Show |
1 | a0018c0018t0002g0131 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1222+918_1222+919i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624001 | ||||||
chr22:30624002
|
A | G | 12 | a0004c0004t0001g0124a0004c0004t0002g0028a0004c0004t0005g0001others(9): Show | 22 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1222+919A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624002 | ||||||
chr22:30624004
|
A | G | 5 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0195others(2): Show | 7 | HG01099.hp2 HG01192.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+921A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624004 | ||||||
chr22:30624004
|
ATG | A | 12 | a0004c0004t0001g0124a0004c0004t0002g0028a0004c0004t0005g0001others(9): Show | 22 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1222+923_1222+924d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624004 | |||||
chr22:30624005
|
TGTATACA others(49): Show |
T | 4 | a0007c0007t0007g0009a0007c0007t0007g0078a0007c0007t0007g0079others(1): Show | 7 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+923_1222+978d others(58): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624005 | ||||||
chr22:30624006
|
G | A | 5 | a0005c0005t0001g0037a0005c0005t0001g0038a0005c0005t0001g0195others(2): Show | 7 | HG01099.hp2 HG01192.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+923G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624006 | ||||||
chr22:30624009
|
T | C | 17 | a0004c0004t0001g0124a0004c0004t0002g0028a0004c0004t0005g0001others(14): Show | 29 | HG01099.hp2 HG01192.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1222+926T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624009 | ||||||
chr22:30624011
|
C | CAT | 74 | a0001c0001t0001g0089a0001c0001t0002g0030a0001c0001t0002g0172others(71): Show | 87 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1222+934_1222+935d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624011 | |||||
chr22:30624011
|
C | CATATATA others(93): Show |
1 | a0001c0001t0021g0156 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1222+944_1222+945i others(102): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624011 | |||||
chr22:30624011
|
C | CATATATA others(15): Show |
1 | a0005c0005t0001g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1222+939_1222+940i others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624011 | |||||
chr22:30624011
|
C | T | 19 | a0004c0004t0001g0124a0004c0004t0002g0028a0004c0004t0005g0001others(16): Show | 31 | HG01099.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1222+928C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624011 | ||||||
chr22:30624019
|
C | T | 5 | a0001c0001t0008g0315a0005c0005t0001g0074a0005c0005t0002g0064others(2): Show | 5 | HG01106.hp1 HG02109.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+936C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624019 | ||||||
chr22:30624023
|
CAT | C | 10 | a0001c0001t0002g0034a0001c0001t0002g0183a0001c0001t0002g0184others(7): Show | 12 | HG01069.hp2 HG01071.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+947_1222+948d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624023 | |||||
chr22:30624025
|
T | C | 41 | a0001c0001t0001g0019a0001c0001t0001g0231a0001c0001t0008g0315others(38): Show | 45 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.1222+942T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624025 | ||||||
chr22:30624027
|
T | C | 13 | a0001c0001t0006g0016a0001c0001t0006g0020a0001c0001t0006g0021others(10): Show | 17 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1222+944T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624027 | ||||||
chr22:30624027
|
T | TGTATACA others(125): Show |
1 | a0001c0001t0001g0231 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1222+944_1222+945i others(134): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624027 | ||||||
chr22:30624032
|
G | A | 3 | a0003c0003t0004g0202a0007c0007t0004g0121a0009c0009t0016g0105 | 3 | HG00323.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1222+949G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624032 | ||||||
chr22:30624033
|
T | C | 1 | a0005c0005t0015g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1222+950T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624033 | ||||||
chr22:30624035
|
T | C | 2 | a0005c0005t0002g0064a0005c0005t0015g0065 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1222+952T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624035 | ||||||
chr22:30624037
|
C | T | 2 | a0005c0005t0002g0066a0005c0005t0002g0068 | 2 | HG00642.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+954C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624037 | ||||||
chr22:30624039
|
T | C | 2 | a0005c0005t0002g0064a0005c0005t0015g0065 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1222+956T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624039 | ||||||
chr22:30624039
|
T | TATATACA others(53): Show |
1 | a0005c0011t0001g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1222+965_1222+966i others(62): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624039 | |||||
chr22:30624041
|
T | C | 2 | a0005c0005t0002g0064a0005c0005t0015g0065 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1222+958T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624041 | ||||||
chr22:30624043
|
T | C | 3 | a0003c0003t0004g0215a0005c0005t0002g0064a0005c0005t0015g0065 | 3 | HG01952.hp2 HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1222+960T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624043 | ||||||
chr22:30624043
|
T | TACACATA others(59): Show |
1 | a0005c0005t0001g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1222+965_1222+966i others(68): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
T | TACACATA others(61): Show |
2 | a0005c0011t0001g0022a0005c0011t0001g0071 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1222+965_1222+966i others(70): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
T | TATACACA others(87): Show |
1 | a0005c0005t0001g0037 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1222+961_1222+962i others(96): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
T | TATACACA others(89): Show |
3 | a0005c0005t0001g0038a0005c0005t0001g0195a0005c0005t0001g0196 | 4 | HG01099.hp2 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+961_1222+962i others(98): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
T | TATACACA others(9): Show |
1 | a0005c0005t0001g0194 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1222+961_1222+962i others(18): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
T | TATACACA others(11): Show |
2 | a0005c0005t0001g0039a0005c0005t0001g0192 | 3 | HG01069.hp2 HG01071.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1222+961_1222+962i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
T | TATACACA others(13): Show |
2 | a0005c0005t0001g0074a0013c0013t0011g0190 | 2 | HG00099.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1222+961_1222+962i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
T | TATACACA others(15): Show |
2 | a0005c0005t0002g0066a0005c0005t0002g0068 | 2 | HG00642.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+961_1222+962i others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
T | TATACACA others(109): Show |
1 | a0005c0005t0011g0354 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1222+961_1222+962i others(118): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
T | TATACATA others(85): Show |
1 | a0013c0013t0011g0191 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1222+961_1222+962i others(94): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
T | TATACATA others(115): Show |
1 | a0005c0005t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+961_1222+962i others(124): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
TAC | T | 16 | a0001c0014t0001g0229a0001c0014t0001g0230a0002c0002t0001g0275others(13): Show | 27 | HG01081.hp1 HG01243.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1222+978_1222+979d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
TACAC | T | 11 | a0001c0001t0001g0231a0003c0003t0004g0198a0003c0003t0004g0210others(8): Show | 11 | HG00280.hp1 HG01081.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1222+976_1222+979d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624043
|
TACACAC | T | 3 | a0001c0001t0003g0088a0001c0001t0003g0316a0009c0009t0016g0105 | 3 | HG00323.hp1 NA19001.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1222+974_1222+979d others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | |||||
chr22:30624045
|
C | CACACACA others(103): Show |
1 | a0010c0012t0001g0227 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1222+969_1222+970i others(112): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624045 | |||||
chr22:30624045
|
C | T | 81 | a0001c0001t0001g0089a0001c0001t0002g0030a0001c0001t0002g0172others(78): Show | 96 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1222+962C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624045 | ||||||
chr22:30624047
|
C | T | 10 | a0004c0004t0002g0028a0004c0004t0005g0001a0004c0004t0005g0110others(7): Show | 20 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1222+964C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624047 | ||||||
chr22:30624049
|
C | CATATATG others(35): Show |
1 | a0003c0003t0004g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1222+967_1222+968i others(44): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATATG others(37): Show |
1 | a0003c0003t0004g0199 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1222+967_1222+968i others(46): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATATG others(91): Show |
1 | a0001c0001t0002g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1222+967_1222+968i others(100): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATATG others(63): Show |
2 | a0001c0001t0002g0165a0001c0001t0002g0166 | 2 | HG02027.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1222+967_1222+968i others(72): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATATG others(65): Show |
3 | a0001c0001t0002g0032a0018c0018t0002g0131a0019c0019t0002g0306 | 4 | NA18949.hp2 NA18950.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+967_1222+968i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATATG others(67): Show |
38 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(35): Show | 57 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1222+967_1222+968i others(76): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATATG others(95): Show |
1 | a0001c0001t0002g0153 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1222+967_1222+968i others(104): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATATG others(65): Show |
1 | a0001c0001t0002g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1222+967_1222+968i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATATG others(67): Show |
8 | a0001c0001t0002g0007a0001c0001t0002g0174a0001c0001t0002g0175others(5): Show | 12 | HG00408.hp1 HG04199.hp2 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+967_1222+968i others(76): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATATG others(67): Show |
1 | a0001c0001t0002g0184 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1222+967_1222+968i others(76): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATATG others(65): Show |
1 | a0001c0001t0002g0169 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1222+967_1222+968i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATGTA others(37): Show |
1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1222+967_1222+968i others(46): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATGTA others(89): Show |
2 | a0004c0004t0005g0114a0004c0004t0005g0115 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1222+967_1222+968i others(98): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624049
|
C | CATATGTA others(87): Show |
1 | a0004c0004t0005g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1222+967_1222+968i others(96): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | |||||
chr22:30624051
|
C | CATACATA others(125): Show |
3 | a0001c0001t0006g0016a0001c0001t0006g0069a0001c0001t0006g0072 | 5 | HG00735.hp1 HG01074.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+969_1222+970i others(134): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATACATA others(153): Show |
1 | a0001c0001t0006g0073 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1222+969_1222+970i others(162): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATACATA others(181): Show |
2 | a0001c0001t0006g0021a0001c0001t0006g0076 | 3 | HG02572.hp1 HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1222+969_1222+970i others(190): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATACATA others(125): Show |
1 | a0001c0001t0006g0020 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1222+969_1222+970i others(134): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATATATA others(11): Show |
1 | a0003c0003t0004g0203 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1222+969_1222+970i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATATATA others(13): Show |
2 | a0009c0009t0003g0026a0009c0009t0003g0102 | 3 | HG01175.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1222+969_1222+970i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATATATA others(11): Show |
1 | a0001c0001t0003g0336 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1222+969_1222+970i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATATATA others(13): Show |
54 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(51): Show | 65 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1222+969_1222+970i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATATATA others(145): Show |
1 | a0001c0001t0001g0019 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1222+969_1222+970i others(154): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATATATA others(15): Show |
2 | a0001c0001t0003g0107a0004c0004t0007g0125 | 2 | HG02683.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1222+969_1222+970i others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATATATA others(41): Show |
5 | a0001c0001t0003g0098a0001c0001t0003g0331a0001c0001t0003g0332others(2): Show | 5 | HG02004.hp1 HG02257.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+969_1222+970i others(50): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATATATG others(11): Show |
11 | a0003c0003t0004g0041a0003c0003t0004g0042a0003c0003t0004g0197others(8): Show | 13 | HG01256.hp1 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1222+969_1222+970i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATATGTA others(175): Show |
1 | a0003c0003t0004g0214 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1222+969_1222+970i others(184): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | CATATGTA others(135): Show |
1 | a0003c0003t0004g0201 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1222+969_1222+970i others(144): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | |||||
chr22:30624051
|
C | T | 8 | a0001c0001t0002g0032a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 9 | HG00639.hp2 HG02027.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+968C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624051 | ||||||
chr22:30624053
|
C | CATATGTA others(203): Show |
1 | a0001c0001t0006g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1222+971_1222+972i others(212): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624053 | |||||
chr22:30624053
|
C | T | 5 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0003g0336others(2): Show | 5 | HG00733.hp1 HG00733.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+970C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624053 | ||||||
chr22:30624055
|
C | T | 15 | a0001c0001t0002g0030a0001c0001t0002g0172a0001c0001t0002g0176others(12): Show | 16 | HG00423.hp2 HG00733.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1222+972C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624055 | ||||||
chr22:30624057
|
C | T | 39 | a0001c0001t0001g0231a0001c0001t0002g0030a0001c0001t0002g0172others(36): Show | 51 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1222+974C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624057 | ||||||
chr22:30624059
|
C | T | 145 | a0001c0001t0001g0089a0001c0001t0001g0231a0001c0001t0002g0002others(142): Show | 186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1222+976C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624059 | ||||||
chr22:30624060
|
A | G | 1 | a0001c0001t0006g0070 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1222+977A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624060 | ||||||
chr22:30624061
|
C | CAT | 5 | a0002c0002t0001g0051a0002c0002t0001g0132a0002c0002t0001g0245others(2): Show | 6 | HG03669.hp2 HG03710.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+997_1222+998d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624061 | |||||
chr22:30624061
|
C | T | 187 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(184): Show | 244 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1222+978C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624061 | ||||||
chr22:30624063
|
T | C | 9 | a0002c0002t0001g0053a0002c0002t0001g0290a0002c0002t0001g0304others(6): Show | 11 | HG00544.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+980T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624063 | ||||||
chr22:30624064
|
A | ATG | 60 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(57): Show | 72 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1222+982_1222+983i others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624064 | |||||
chr22:30624064
|
A | G | 3 | a0001c0001t0003g0088a0001c0001t0003g0316a0009c0009t0016g0105 | 3 | HG00323.hp1 NA19001.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1222+981A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624064 | ||||||
chr22:30624068
|
A | G | 7 | a0001c0001t0006g0016a0001c0001t0006g0020a0001c0001t0006g0021others(4): Show | 11 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+985A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624068 | ||||||
chr22:30624070
|
A | G | 1 | a0001c0001t0006g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1222+987A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624070 | ||||||
chr22:30624076
|
A | G | 1 | a0002c0002t0001g0150 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1222+993A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624076 | ||||||
chr22:30624077
|
TA | T | 3 | a0001c0001t0002g0030a0001c0001t0002g0176a0001c0001t0021g0156 | 4 | HG01981.hp2 NA18979.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+995delA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624077 | ||||||
chr22:30624078
|
A | AT | 3 | a0001c0001t0002g0172a0005c0005t0001g0074a0013c0013t0011g0190 | 3 | HG00099.hp2 HG00423.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1222+996dupT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624078 | |||||
chr22:30624078
|
A | T | 16 | a0001c0001t0001g0231a0001c0014t0001g0229a0002c0002t0001g0262others(13): Show | 19 | HG00642.hp2 HG01192.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1222+995A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624078 | ||||||
chr22:30624080
|
A | AT | 12 | a0001c0001t0002g0027a0001c0001t0002g0109a0001c0001t0002g0120others(9): Show | 14 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1222+1009dupT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | |||||
chr22:30624080
|
A | ATAT | 9 | a0001c0001t0002g0006a0001c0001t0002g0133a0001c0001t0002g0134others(6): Show | 13 | HG00621.hp1 HG01261.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1222+998_1222+999i others(5): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | |||||
chr22:30624080
|
A | ATATT | 8 | a0003c0003t0004g0041a0003c0003t0004g0197a0003c0003t0004g0203others(5): Show | 9 | HG01256.hp1 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+998_1222+999i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | |||||
chr22:30624080
|
A | ATATTT | 12 | a0001c0001t0002g0036a0001c0001t0002g0174a0001c0001t0002g0188others(9): Show | 16 | HG00673.hp1 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1222+998_1222+999i others(7): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | |||||
chr22:30624080
|
A | ATT | 5 | a0001c0001t0002g0163a0002c0002t0001g0047a0004c0004t0005g0123others(2): Show | 6 | HG02698.hp1 HG03579.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+1008_1222+100 others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | |||||
chr22:30624080
|
A | ATTT | 32 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(29): Show | 49 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1222+1007_1222+100 others(7): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | |||||
chr22:30624080
|
A | ATTTT | 7 | a0001c0001t0001g0019a0003c0003t0004g0042a0003c0003t0004g0206others(4): Show | 10 | HG00140.hp1 HG01496.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1222+1006_1222+100 others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | |||||
chr22:30624080
|
A | T | 63 | a0001c0001t0001g0231a0001c0001t0002g0030a0001c0001t0002g0172others(60): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1222+997A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624080 | ||||||
chr22:30624082
|
T | A | 68 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(65): Show | 81 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1222+999T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624082 | ||||||
chr22:30624084
|
T | A | 22 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(19): Show | 31 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1222+1001T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624084 | ||||||
chr22:30624085
|
T | A | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+1002T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624085 | ||||||
chr22:30624103
|
C | T | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1222+1020C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624103 | ||||||
chr22:30624126
|
G | A | 213 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(210): Show | 275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1222+1043G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624126 | ||||||
chr22:30624127
|
T | C | 39 | a0001c0001t0001g0231a0001c0014t0001g0229a0001c0014t0001g0230others(36): Show | 45 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.1222+1044T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624127 | ||||||
chr22:30624165
|
T | C | 213 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(210): Show | 275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1222+1082T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624165 | ||||||
chr22:30624293
|
C | CA | 3 | a0005c0011t0001g0022a0005c0011t0001g0071a0005c0011t0001g0077 | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+1213dupA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624293 | |||||
chr22:30624354
|
G | T | 41 | a0001c0001t0001g0019a0001c0001t0001g0231a0001c0014t0001g0229others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.1222+1271G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624354 | ||||||
chr22:30624403
|
C | T | 1 | a0005c0005t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1222+1320C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624403 | ||||||
chr22:30624413
|
T | C | 225 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0231others(222): Show | 289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1222+1330T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624413 | ||||||
chr22:30624514
|
C | A | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1431C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624514 | ||||||
chr22:30624517
|
A | C | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1434A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624517 | ||||||
chr22:30624518
|
G | T | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1435G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624518 | ||||||
chr22:30624520
|
G | A | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1437G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624520 | ||||||
chr22:30624523
|
C | A | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1440C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624523 | ||||||
chr22:30624524
|
C | G | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1441C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624524 | ||||||
chr22:30624525
|
C | A | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1442C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624525 | ||||||
chr22:30624526
|
A | G | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1443A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624526 | ||||||
chr22:30624527
|
C | G | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1444C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624527 | ||||||
chr22:30624529
|
A | G | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1446A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624529 | ||||||
chr22:30624532
|
A | G | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1449A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624532 | ||||||
chr22:30624533
|
A | G | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1450A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624533 | ||||||
chr22:30624534
|
G | T | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1451G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624534 | ||||||
chr22:30624535
|
C | G | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1452C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624535 | ||||||
chr22:30624536
|
A | ATTC | 75 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1222+1456_1222+145 others(7): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624536 | |||||
chr22:30624542
|
T | G | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1459T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624542 | ||||||
chr22:30624544
|
C | G | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1461C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624544 | ||||||
chr22:30624547
|
G | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+1464G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624547 | ||||||
chr22:30624548
|
C | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+1465C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624548 | ||||||
chr22:30624550
|
C | A | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1467C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624550 | ||||||
chr22:30624556
|
C | T | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1473C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624556 | ||||||
chr22:30624561
|
T | C | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+1478T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624561 | ||||||
chr22:30624647
|
C | T | 1 | a0005c0005t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1222+1564C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624647 | ||||||
chr22:30624669
|
C | A | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1586C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624669 | ||||||
chr22:30624693
|
A | G | 5 | a0005c0005t0002g0064a0005c0005t0002g0066a0005c0005t0002g0067others(2): Show | 5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+1610A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624693 | ||||||
chr22:30624732
|
C | T | 1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1222+1649C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624732 | ||||||
chr22:30624783
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0108a0001c0001t0002g0109 | 4 | HG01070.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223-1677C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624783 | ||||||
chr22:30624816
|
A | G | 4 | a0010c0012t0001g0225a0010c0012t0001g0226a0010c0012t0001g0227others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223-1644A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624816 | ||||||
chr22:30624853
|
T | C | 3 | a0005c0011t0001g0022a0005c0011t0001g0071a0005c0011t0001g0077 | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223-1607T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624853 | ||||||
chr22:30624857
|
G | T | 1 | a0001c0001t0003g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1223-1603G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624857 | ||||||
chr22:30624915
|
C | G | 1 | a0001c0001t0010g0104 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1223-1545C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624915 | ||||||
chr22:30624973
|
T | C | 1 | a0005c0005t0002g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1223-1487T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624973 | ||||||
chr22:30624988
|
A | C | 66 | a0001c0001t0001g0089a0001c0001t0003g0010a0001c0001t0003g0011others(63): Show | 78 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1223-1472A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624988 | ||||||
chr22:30625062
|
C | G | 61 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1223-1398C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625062 | ||||||
chr22:30625113
|
G | A | 1 | a0003c0003t0004g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1223-1347G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625113 | ||||||
chr22:30625223
|
T | A | 5 | a0005c0005t0002g0064a0005c0005t0002g0066a0005c0005t0002g0067others(2): Show | 5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1223-1237T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625223 | ||||||
chr22:30625297
|
C | T | 1 | a0003c0003t0004g0199 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1223-1163C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625297 | ||||||
chr22:30625315
|
GGGGCCCA others(28): Show |
G | 1 | a0003c0003t0004g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1223-1144_1223-111 others(39): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625315 | ||||||
chr22:30625348
|
GT | G | 14 | a0002c0002t0001g0005a0002c0002t0001g0029a0002c0002t0001g0128others(11): Show | 16 | HG00597.hp2 HG02015.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1223-1110delT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30625348 | |||||
chr22:30625366
|
G | A | 2 | a0002c0002t0001g0137a0002c0002t0001g0140 | 2 | HG00735.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1223-1094G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625366 | ||||||
chr22:30625378
|
T | A | 3 | a0001c0001t0002g0133a0001c0001t0002g0134a0001c0001t0002g0164 | 3 | HG02074.hp2 HG02083.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1223-1082T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625378 | ||||||
chr22:30625402
|
TA | T | 36 | a0003c0003t0004g0040a0003c0003t0004g0041a0003c0003t0004g0042others(33): Show | 42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1223-1046delA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30625402 | |||||
chr22:30625402
|
TAA | T | 251 | a0001c0001t0001g0019a0001c0001t0001g0231a0001c0001t0002g0002others(248): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1223-1047_1223-104 others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30625402 | |||||
chr22:30625405
|
A | T | 5 | a0005c0005t0001g0039a0005c0005t0001g0194a0005c0005t0011g0354others(2): Show | 6 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1223-1055A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625405 | ||||||
chr22:30625411
|
A | T | 1 | a0007c0007t0007g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1223-1049A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625411 | ||||||
chr22:30625413
|
A | T | 8 | a0003c0003t0004g0202a0003c0003t0004g0203a0007c0007t0004g0121others(5): Show | 11 | HG01261.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1223-1047A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625413 | ||||||
chr22:30625415
|
T | A | 1 | a0001c0001t0010g0104 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1223-1045T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625415 | ||||||
chr22:30625425
|
G | T | 61 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1223-1035G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625425 | ||||||
chr22:30625469
|
A | T | 1 | a0002c0002t0001g0149 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1223-991A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625469 | ||||||
chr22:30625470
|
T | A | 7 | a0001c0001t0001g0019a0002c0002t0001g0282a0002c0002t0001g0286others(4): Show | 8 | HG01496.hp2 HG02056.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1223-990T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625470 | ||||||
chr22:30625595
|
T | G | 1 | a0003c0003t0004g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1223-865T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625595 | ||||||
chr22:30625623
|
C | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1223-837C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625623 | ||||||
chr22:30625690
|
C | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1223-770C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625690 | ||||||
chr22:30625823
|
C | G | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1223-637C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625823 | ||||||
chr22:30625830
|
C | G | 4 | a0009c0009t0003g0026a0009c0009t0003g0102a0009c0009t0003g0106others(1): Show | 5 | HG00323.hp1 HG01175.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1223-630C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625830 | ||||||
chr22:30626067
|
A | T | 2 | a0001c0001t0002g0120a0001c0001t0002g0159 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1223-393A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626067 | ||||||
chr22:30626097
|
T | G | 1 | a0001c0001t0002g0027 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1223-363T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626097 | ||||||
chr22:30626108
|
T | G | 61 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1223-352T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626108 | ||||||
chr22:30626166
|
C | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1223-294C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626166 | ||||||
chr22:30626213
|
A | G | 1 | a0001c0001t0003g0100 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1223-247A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626213 | ||||||
chr22:30626254
|
C | T | 1 | a0010c0012t0020g0228 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1223-206C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626254 | ||||||
chr22:30626275
|
G | T | 5 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0210others(2): Show | 5 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1223-185G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626275 | ||||||
chr22:30626285
|
G | A | 212 | a0001c0001t0001g0089a0001c0001t0001g0231a0001c0001t0002g0002others(209): Show | 273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1223-175G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626285 | ||||||
chr22:30626292
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T | C | 16 | a0004c0004t0001g0124a0004c0004t0002g0028a0004c0004t0005g0001others(13): Show | 26 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1223-168T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626292 | ||||||
chr22:30626314
|
G | A | 36 | a0003c0003t0004g0040a0003c0003t0004g0041a0003c0003t0004g0042others(33): Show | 42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1223-146G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626314 |