geneid | 92749 |
---|---|
ensemblid | ENSG00000157856.12 |
hgncid | 24245 |
symbol | DRC1 |
name | dynein regulatory complex subunit 1 |
refseq_nuc | NM_145038.5 |
refseq_prot | NP_659475.2 |
ensembl_nuc | ENST00000288710.7 |
ensembl_prot | ENSP00000288710.2 |
mane_status | MANE Select |
chr | chr2 |
start | 26401920 |
end | 26456711 |
strand | + |
ver | v1.2 |
region | chr2:26401920-26456711 |
region5000 | chr2:26396920-26461711 |
regionname0 | DRC1_chr2_26401920_26456711 |
regionname5000 | DRC1_chr2_26396920_26461711 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001 | 0/1 | 740 | 127 | 45 | 29 | 30 | 6 | 16 | 29 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0002 | 0/0 | 740 | 101 | 2 | 17 | 80 | 0 | 2 | 60 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0003 | 0/0 | 740 | 49 | 31 | 9 | 8 | 0 | 1 | 5 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0004 | 0/0 | 740 | 40 | 0 | 7 | 21 | 2 | 10 | 15 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0005 | 0/0 | 740 | 14 | 0 | 4 | 10 | 0 | 0 | 6 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0006 | 0/0 | 740 | 10 | 0 | 0 | 10 | 0 | 0 | 5 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0007 | 0/0 | 740 | 9 | 0 | 0 | 7 | 0 | 2 | 4 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0008 | 0/0 | 740 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0009 | 0/0 | 740 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0010 | 0/0 | 740 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0011 | 0/0 | 740 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0012 | 0/0 | 740 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0013 | 0/0 | 740 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0014 | 0/0 | 740 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0015 | 0/0 | 740 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0016 | 0/0 | 740 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0017 | 0/0 | 740 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0018 | 0/0 | 740 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0019 | 0/0 | 735 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0020 | 0/0 | 740 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0021 | 0/0 | 740 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0022 | 0/0 | 740 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0023 | 1/0 | 740 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2223 | 111 | 32 | 29 | 27 | 6 | 16 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0002 | 0/0 | 2223 | 100 | 2 | 16 | 80 | 0 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0003 | 0/0 | 2223 | 39 | 0 | 7 | 20 | 2 | 10 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0004 | 0/0 | 2223 | 29 | 20 | 7 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0005 | 0/0 | 2223 | 19 | 10 | 2 | 6 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0006 | 0/0 | 2223 | 14 | 0 | 4 | 10 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0007 | 0/0 | 2223 | 13 | 10 | 0 | 3 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0008 | 0/0 | 2223 | 10 | 0 | 0 | 10 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0009 | 0/0 | 2223 | 9 | 0 | 0 | 7 | 0 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0010 | 0/0 | 2223 | 4 | 3 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0011 | 0/0 | 2223 | 4 | 4 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0012 | 0/0 | 2223 | 4 | 4 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0013 | 0/0 | 2223 | 4 | 0 | 2 | 0 | 2 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0014 | 0/0 | 2223 | 3 | 1 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0015 | 0/0 | 2223 | 3 | 2 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0016 | 0/0 | 2223 | 3 | 3 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0017 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0018 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0019 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0020 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0021 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0022 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0023 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0024 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0025 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0026 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0027 | 0/0 | 2208 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0028 | 1/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0029 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0030 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
c0031 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 265 | 322 | 67 | 70 | 146 | 8 | 30 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
t0002 | 0/0 | 265 | 26 | 1 | 2 | 23 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
t0003 | 0/0 | 265 | 25 | 24 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
t0004 | 0/1 | 265 | 6 | 0 | 1 | 0 | 2 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
t0005 | 0/0 | 265 | 2 | 2 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
t0006 | 0/0 | 265 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
t0007 | 0/0 | 265 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
t0008 | 0/0 | 265 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0277 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0021 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0001 | 0/1 | 2223 | 111 | 32 | 29 | 27 | 6 | 16 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0007 | 0/0 | 2223 | 13 | 10 | 0 | 3 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0016 | 0/0 | 2223 | 3 | 3 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0002c0002 | 0/0 | 2223 | 100 | 2 | 16 | 80 | 0 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0002c0018 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0003c0004 | 0/0 | 2223 | 29 | 20 | 7 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0003c0005 | 0/0 | 2223 | 19 | 10 | 2 | 6 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0003c0025 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0004c0003 | 0/0 | 2223 | 39 | 0 | 7 | 20 | 2 | 10 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0004c0029 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0005c0006 | 0/0 | 2223 | 14 | 0 | 4 | 10 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0006c0008 | 0/0 | 2223 | 10 | 0 | 0 | 10 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0007c0009 | 0/0 | 2223 | 9 | 0 | 0 | 7 | 0 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0008c0011 | 0/0 | 2223 | 4 | 4 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0008c0012 | 0/0 | 2223 | 4 | 4 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0009c0010 | 0/0 | 2223 | 4 | 3 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0010c0013 | 0/0 | 2223 | 4 | 0 | 2 | 0 | 2 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0011c0015 | 0/0 | 2223 | 3 | 2 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0012c0014 | 0/0 | 2223 | 3 | 1 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0013c0017 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0014c0019 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0015c0031 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0016c0030 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0017c0022 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0018c0023 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0019c0027 | 0/0 | 2208 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0020c0026 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0021c0024 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0022c0020 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0023c0028 | 1/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0021t0003 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0001t0001 | 0/0 | 2487 | 79 | 26 | 28 | 7 | 4 | 14 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0001t0002 | 0/0 | 2487 | 20 | 0 | 0 | 20 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0001t0003 | 0/0 | 2487 | 5 | 5 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0001t0004 | 0/1 | 2487 | 6 | 0 | 1 | 0 | 2 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0001t0007 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0007t0001 | 0/0 | 2487 | 8 | 7 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0007t0002 | 0/0 | 2487 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0007t0003 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0001c0016t0003 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0002c0002t0001 | 0/0 | 2487 | 99 | 2 | 16 | 79 | 0 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0002c0002t0006 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0002c0018t0001 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0003c0004t0001 | 0/0 | 2487 | 20 | 13 | 5 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0003c0004t0002 | 0/0 | 2487 | 3 | 1 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0003c0004t0003 | 0/0 | 2487 | 6 | 6 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0003c0005t0001 | 0/0 | 2487 | 12 | 4 | 1 | 6 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0003c0005t0003 | 0/0 | 2487 | 7 | 6 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0003c0025t0001 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0004c0003t0001 | 0/0 | 2487 | 39 | 0 | 7 | 20 | 2 | 10 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0004c0029t0001 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0005c0006t0001 | 0/0 | 2487 | 14 | 0 | 4 | 10 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0006c0008t0001 | 0/0 | 2487 | 10 | 0 | 0 | 10 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0007c0009t0001 | 0/0 | 2487 | 9 | 0 | 0 | 7 | 0 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0008c0011t0001 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0008c0011t0005 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0008c0012t0001 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0008c0012t0008 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0009c0010t0001 | 0/0 | 2487 | 4 | 3 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0010c0013t0001 | 0/0 | 2487 | 4 | 0 | 2 | 0 | 2 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0011c0015t0001 | 0/0 | 2487 | 3 | 2 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0012c0014t0001 | 0/0 | 2487 | 3 | 1 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0013c0017t0005 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0014c0019t0001 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0015c0031t0001 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0016c0030t0001 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0017c0022t0001 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0018c0023t0001 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0019c0027t0001 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0020c0026t0001 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0021c0024t0002 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0022c0020t0001 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
a0023c0028t0001 | 1/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | copy fasta | chr2 | 26396920 | 26461711 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0021t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0004g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0007t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0016t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0016t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0001c0016t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0002t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0002c0018t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0004t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0005t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0003c0025t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0003t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0004c0029t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0005c0006t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0006c0008t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0006c0008t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0006c0008t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0006c0008t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0006c0008t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0006c0008t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0006c0008t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0006c0008t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0006c0008t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0006c0008t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0007c0009t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0007c0009t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0007c0009t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0007c0009t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0007c0009t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0007c0009t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0007c0009t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0007c0009t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0007c0009t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0008c0011t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0008c0011t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0008c0011t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0008c0011t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0008c0012t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0008c0012t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0008c0012t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0008c0012t0008g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0009c0010t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0009c0010t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0009c0010t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0010c0013t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0010c0013t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0010c0013t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0010c0013t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0011c0015t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0011c0015t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0012c0014t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0012c0014t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0012c0014t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0013c0017t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0014c0019t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0015c0031t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0016c0030t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0017c0022t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0018c0023t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0019c0027t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0020c0026t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0021c0024t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0022c0020t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
a0023c0028t0001g0277 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0250 | EUR | GBR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00280 | hp1 | a0004 | c0003 | t0001 | g0197 | EUR | FIN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00408 | hp1 | a0006 | c0008 | t0001 | g0179 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00438 | hp2 | a0005 | c0006 | t0001 | g0241 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00544 | hp1 | a0004 | c0003 | t0001 | g0218 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00558 | hp2 | a0003 | c0005 | t0001 | g0307 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00609 | hp1 | a0003 | c0004 | t0001 | g0107 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00609 | hp2 | a0007 | c0009 | t0001 | g0186 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00639 | hp1 | a0010 | c0013 | t0001 | g0205 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00642 | hp1 | a0003 | c0004 | t0001 | g0328 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00642 | hp2 | a0010 | c0013 | t0001 | g0199 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | CHS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00733 | hp1 | a0012 | c0014 | t0001 | g0325 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0213 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00735 | hp2 | a0004 | c0003 | t0001 | g0202 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00738 | hp1 | a0009 | c0010 | t0001 | g0267 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00738 | hp2 | a0004 | c0003 | t0001 | g0207 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG00741 | hp2 | a0003 | c0004 | t0001 | g0360 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01109 | hp1 | a0003 | c0005 | t0001 | g0063 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01109 | hp2 | a0019 | c0027 | t0001 | g0344 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01167 | hp2 | a0012 | c0014 | t0001 | g0311 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01168 | hp2 | a0003 | c0004 | t0002 | g0283 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01169 | hp2 | a0003 | c0004 | t0002 | g0284 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01192 | hp1 | a0004 | c0003 | t0001 | g0216 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01243 | hp2 | a0011 | c0015 | t0001 | g0016 | AMR | PUR | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01255 | hp2 | a0004 | c0003 | t0001 | g0230 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0121 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01261 | hp1 | a0014 | c0019 | t0001 | g0365 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01346 | hp2 | a0003 | c0004 | t0001 | g0319 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01358 | hp1 | a0002 | c0018 | t0001 | g0008 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01358 | hp2 | a0004 | c0003 | t0001 | g0322 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01361 | hp1 | a0005 | c0006 | t0001 | g0247 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01433 | hp2 | a0003 | c0004 | t0001 | g0329 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01496 | hp1 | a0003 | c0005 | t0003 | g0358 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01515 | hp1 | a0010 | c0013 | t0001 | g0196 | EUR | IBS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0075 | EUR | IBS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01517 | hp2 | a0010 | c0013 | t0001 | g0223 | EUR | IBS | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0352 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01891 | hp2 | a0008 | c0011 | t0001 | g0333 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01934 | hp1 | a0003 | c0004 | t0001 | g0029 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0271 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01978 | hp2 | a0004 | c0003 | t0001 | g0227 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02004 | hp1 | a0005 | c0006 | t0001 | g0243 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02015 | hp1 | a0004 | c0003 | t0001 | g0249 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02027 | hp1 | a0006 | c0008 | t0001 | g0187 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02027 | hp2 | a0003 | c0004 | t0001 | g0172 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02040 | hp2 | a0004 | c0003 | t0001 | g0217 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02055 | hp2 | a0015 | c0031 | t0001 | g0364 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02071 | hp1 | a0006 | c0008 | t0001 | g0175 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02071 | hp2 | a0004 | c0003 | t0001 | g0236 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02074 | hp1 | a0005 | c0006 | t0001 | g0239 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0355 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02080 | hp2 | a0006 | c0008 | t0001 | g0178 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02129 | hp1 | a0005 | c0006 | t0001 | g0226 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02132 | hp1 | a0004 | c0003 | t0001 | g0233 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02135 | hp1 | a0007 | c0009 | t0001 | g0189 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02145 | hp1 | a0009 | c0010 | t0001 | g0281 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0169 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | CDX | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02165 | hp2 | a0004 | c0003 | t0001 | g0252 | EAS | CDX | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02258 | hp1 | a0003 | c0004 | t0001 | g0316 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02258 | hp2 | a0003 | c0004 | t0002 | g0296 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02273 | hp2 | a0005 | c0006 | t0001 | g0248 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02300 | hp2 | a0005 | c0006 | t0001 | g0012 | AMR | PEL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02523 | hp2 | a0006 | c0008 | t0001 | g0184 | EAS | KHV | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02572 | hp1 | a0003 | c0005 | t0003 | g0362 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02602 | hp2 | a0004 | c0003 | t0001 | g0232 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02622 | hp1 | a0001 | c0007 | t0001 | g0353 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02622 | hp2 | a0003 | c0004 | t0003 | g0321 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02630 | hp2 | a0001 | c0007 | t0001 | g0350 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02647 | hp2 | a0016 | c0030 | t0001 | g0361 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02698 | hp1 | a0004 | c0003 | t0001 | g0201 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02717 | hp1 | a0001 | c0007 | t0003 | g0351 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02723 | hp1 | a0003 | c0005 | t0001 | g0018 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02735 | hp1 | a0022 | c0020 | t0001 | g0028 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02809 | hp1 | a0003 | c0005 | t0001 | g0020 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02809 | hp2 | a0003 | c0004 | t0001 | g0337 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02818 | hp1 | a0001 | c0016 | t0003 | g0280 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02818 | hp2 | a0003 | c0005 | t0001 | g0019 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02886 | hp1 | a0001 | c0007 | t0003 | g0266 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02886 | hp2 | a0008 | c0012 | t0001 | g0257 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02895 | hp2 | a0003 | c0004 | t0003 | g0312 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02897 | hp1 | a0003 | c0004 | t0003 | g0313 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02922 | hp1 | a0008 | c0011 | t0005 | g0310 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02922 | hp2 | a0003 | c0005 | t0003 | g0331 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02965 | hp1 | a0009 | c0010 | t0001 | g0013 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02965 | hp2 | a0003 | c0004 | t0001 | g0317 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02970 | hp1 | a0003 | c0004 | t0001 | g0318 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02976 | hp1 | a0008 | c0012 | t0001 | g0343 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03041 | hp1 | a0003 | c0005 | t0003 | g0261 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03041 | hp2 | a0003 | c0005 | t0003 | g0276 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03098 | hp2 | a0003 | c0004 | t0001 | g0263 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03130 | hp1 | a0003 | c0004 | t0001 | g0260 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03130 | hp2 | a0003 | c0004 | t0001 | g0320 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03139 | hp1 | a0001 | c0016 | t0003 | g0279 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03195 | hp1 | a0003 | c0005 | t0003 | g0359 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03195 | hp2 | a0009 | c0010 | t0001 | g0013 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03209 | hp2 | a0003 | c0005 | t0001 | g0022 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03225 | hp1 | a0000 | c0021 | t0003 | g0327 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03239 | hp1 | a0003 | c0005 | t0001 | g0054 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03453 | hp1 | a0008 | c0012 | t0001 | g0258 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03486 | hp1 | a0003 | c0004 | t0001 | g0342 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03486 | hp2 | a0003 | c0004 | t0001 | g0262 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03490 | hp2 | a0004 | c0003 | t0001 | g0222 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03491 | hp2 | a0004 | c0003 | t0001 | g0219 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03492 | hp1 | a0004 | c0003 | t0001 | g0221 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03516 | hp1 | a0003 | c0004 | t0001 | g0326 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03516 | hp2 | a0003 | c0005 | t0003 | g0363 | AFR | ESN | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03540 | hp2 | a0001 | c0007 | t0001 | g0349 | AFR | GWD | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03579 | hp1 | a0012 | c0014 | t0001 | g0051 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03579 | hp2 | a0001 | c0007 | t0001 | g0092 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03654 | hp2 | a0004 | c0003 | t0001 | g0206 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03669 | hp2 | a0004 | c0003 | t0001 | g0194 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03831 | hp1 | a0004 | c0003 | t0001 | g0045 | SAS | BEB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | BEB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0149 | SAS | BEB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0090 | SAS | BEB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG04199 | hp1 | a0007 | c0009 | t0001 | g0190 | SAS | STU | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG04199 | hp2 | a0004 | c0003 | t0001 | g0049 | SAS | STU | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG04204 | hp2 | a0007 | c0009 | t0001 | g0174 | SAS | STU | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18522 | hp1 | a0011 | c0015 | t0001 | g0357 | AFR | YRI | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18612 | hp1 | a0007 | c0009 | t0001 | g0182 | EAS | CHB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18612 | hp2 | a0005 | c0006 | t0001 | g0235 | EAS | CHB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | CHB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | CHB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18906 | hp1 | a0003 | c0004 | t0001 | g0024 | AFR | YRI | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18940 | hp1 | a0005 | c0006 | t0001 | g0238 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18940 | hp2 | a0007 | c0009 | t0001 | g0191 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18941 | hp1 | a0006 | c0008 | t0001 | g0181 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18942 | hp2 | a0003 | c0005 | t0001 | g0274 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18944 | hp2 | a0003 | c0005 | t0001 | g0275 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18945 | hp2 | a0004 | c0003 | t0001 | g0137 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18946 | hp1 | a0002 | c0002 | t0006 | g0097 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18946 | hp2 | a0004 | c0003 | t0001 | g0012 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18954 | hp1 | a0005 | c0006 | t0001 | g0246 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0354 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18963 | hp1 | a0004 | c0003 | t0001 | g0242 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18964 | hp1 | a0004 | c0003 | t0001 | g0088 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18965 | hp2 | a0004 | c0003 | t0001 | g0244 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18966 | hp1 | a0006 | c0008 | t0001 | g0180 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18966 | hp2 | a0003 | c0005 | t0001 | g0299 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18974 | hp1 | a0006 | c0008 | t0001 | g0188 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18979 | hp1 | a0005 | c0006 | t0001 | g0245 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18979 | hp2 | a0003 | c0005 | t0001 | g0298 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18980 | hp1 | a0004 | c0003 | t0001 | g0200 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18984 | hp1 | a0006 | c0008 | t0001 | g0177 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18991 | hp1 | a0005 | c0006 | t0001 | g0254 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18993 | hp1 | a0001 | c0007 | t0002 | g0295 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19002 | hp1 | a0001 | c0007 | t0001 | g0144 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19002 | hp2 | a0005 | c0006 | t0001 | g0240 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19003 | hp1 | a0017 | c0022 | t0001 | g0173 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19003 | hp2 | a0004 | c0003 | t0001 | g0273 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19004 | hp1 | a0004 | c0003 | t0001 | g0058 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19004 | hp2 | a0020 | c0026 | t0001 | g0114 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19007 | hp1 | a0007 | c0009 | t0001 | g0185 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19030 | hp1 | a0008 | c0012 | t0008 | g0346 | AFR | LWK | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19030 | hp2 | a0001 | c0007 | t0001 | g0348 | AFR | LWK | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0050 | AFR | LWK | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19043 | hp2 | a0003 | c0004 | t0003 | g0264 | AFR | LWK | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19054 | hp2 | a0004 | c0003 | t0001 | g0228 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19057 | hp1 | a0018 | c0023 | t0001 | g0198 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19058 | hp2 | a0004 | c0003 | t0001 | g0229 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19065 | hp1 | a0007 | c0009 | t0001 | g0183 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19066 | hp1 | a0007 | c0009 | t0001 | g0128 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19066 | hp2 | a0004 | c0029 | t0001 | g0109 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19067 | hp2 | a0004 | c0003 | t0001 | g0256 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19070 | hp2 | a0001 | c0007 | t0002 | g0293 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19075 | hp1 | a0004 | c0003 | t0001 | g0234 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19075 | hp2 | a0003 | c0005 | t0001 | g0300 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19081 | hp2 | a0021 | c0024 | t0002 | g0294 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19085 | hp2 | a0004 | c0003 | t0001 | g0255 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19086 | hp2 | a0004 | c0003 | t0001 | g0231 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19088 | hp1 | a0005 | c0006 | t0001 | g0237 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19088 | hp2 | a0006 | c0008 | t0001 | g0176 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19240 | hp1 | a0001 | c0007 | t0003 | g0269 | AFR | YRI | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA19240 | hp2 | a0001 | c0007 | t0001 | g0270 | AFR | YRI | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA20129 | hp1 | a0003 | c0025 | t0001 | g0356 | AFR | ASW | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA20129 | hp2 | a0001 | c0007 | t0001 | g0251 | AFR | ASW | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA20805 | hp2 | a0004 | c0003 | t0001 | g0193 | EUR | TSI | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA20905 | hp2 | a0004 | c0003 | t0001 | g0214 | SAS | GIH | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG01123 | hp2 | a0004 | c0003 | t0001 | g0215 | AMR | CLM | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02109 | hp2 | a0008 | c0011 | t0001 | g0323 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02486 | hp1 | a0001 | c0016 | t0003 | g0278 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02559 | hp1 | a0003 | c0004 | t0003 | g0025 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG02559 | hp2 | a0011 | c0015 | t0001 | g0016 | AFR | ACB | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03471 | hp1 | a0008 | c0011 | t0001 | g0324 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | USA | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | USA | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA20300 | hp1 | a0013 | c0017 | t0005 | g0309 | AFR | USA | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA20300 | hp2 | a0003 | c0004 | t0001 | g0259 | AFR | USA | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA21309 | hp1 | a0003 | c0004 | t0001 | g0314 | AFR | LWK | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
NA21309 | hp2 | a0003 | c0004 | t0003 | g0265 | AFR | LWK | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0212 | REF | REF | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
homoSapiens_grch38 | hp1 | a0023 | c0028 | t0001 | g0277 | REF | REF | DRC1_chr2_26396920_26461711 | DRC1 | chr2 | 26396920 | 26461711 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26414360
|
T | C | 4 | a0008a0011a0012others(1): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
missense_variant | MODERATE | c.172T>C | p.Tyr58His | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/17 | 242/2487 | 172/2223 | 58/740 | chr2 | 26414360 | ||
chr2:26414425
|
C | A | 1 | a0014 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.237C>A | p.Ser79Arg | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/17 | 307/2487 | 237/2223 | 79/740 | chr2 | 26414425 | ||
chr2:26440398
|
G | T | 1 | a0011 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.909G>T | p.Gln303His | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/17 | 979/2487 | 909/2223 | 303/740 | chr2 | 26440398 | ||
chr2:26440481
|
C | T | 2 | a0015a0016 | 2 | HG02055.hp2 HG02647.hp2 |
missense_variant | MODERATE | c.992C>T | p.Thr331Ile | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/17 | 1062/2487 | 992/2223 | 331/740 | chr2 | 26440481 | ||
chr2:26444260
|
C | T | 3 | a0006a0007a0011 | 22 | HG00408.hp1 HG00609.hp2 HG01243.hp2 others(19): Show |
missense_variant | MODERATE | c.1067C>T | p.Ala356Val | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 9/17 | 1137/2487 | 1067/2223 | 356/740 | chr2 | 26444260 | ||
chr2:26444262
|
A | G | 4 | a0004a0005a0017others(1): Show | 56 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(53): Show |
missense_variant | MODERATE | c.1069A>G | p.Lys357Glu | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 9/17 | 1139/2487 | 1069/2223 | 357/740 | chr2 | 26444262 | ||
chr2:26444747
|
T | C | 23 | a0000a0001a0002others(20): Show | 383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
missense_variant | MODERATE | c.1195T>C | p.Trp399Arg | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/17 | 1265/2487 | 1195/2223 | 399/740 | chr2 | 26444747 | ||
chr2:26450005
|
A | C | 1 | a0018 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1519A>C | p.Ile507Leu | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 12/17 | 1589/2487 | 1519/2223 | 507/740 | chr2 | 26450005 | ||
chr2:26450071
|
G | A | 1 | a0022 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1585G>A | p.Asp529Asn | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 12/17 | 1655/2487 | 1585/2223 | 529/740 | chr2 | 26450071 | ||
chr2:26453335
|
CAGGCGAG others(8): Show |
C | 1 | a0019 | 1 | HG01109.hp2 | conservative_inframe_deletion | MODERATE | c.1720_1734delAAGGCG others(9): Show |
p.Lys574_Glu578del | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/17 | 1790/2487 | 1720/2223 | 574/740 | INFO_REALIGN_3_PRIME | chr2 | 26453335 | |
chr2:26453354
|
C | T | 1 | a0013 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1724C>T | p.Ala575Val | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/17 | 1794/2487 | 1724/2223 | 575/740 | chr2 | 26453354 | ||
chr2:26453527
|
G | T | 5 | a0002a0006a0014others(2): Show | 114 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
missense_variant | MODERATE | c.1897G>T | p.Val633Phe | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/17 | 1967/2487 | 1897/2223 | 633/740 | chr2 | 26453527 | ||
chr2:26454703
|
C | T | 1 | a0009 | 4 | HG00738.hp1 HG02145.hp1 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.1976C>T | p.Ser659Leu | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 15/17 | 2046/2487 | 1976/2223 | 659/740 | chr2 | 26454703 | ||
chr2:26455172
|
G | T | 4 | a0003a0011a0012others(1): Show | 56 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(53): Show |
missense_variant | MODERATE | c.2105G>T | p.Ser702Ile | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/17 | 2175/2487 | 2105/2223 | 702/740 | chr2 | 26455172 | ||
chr2:26455214
|
A | C | 2 | a0005a0021 | 15 | HG00438.hp2 HG01361.hp1 HG02004.hp1 others(12): Show |
missense_variant | MODERATE | c.2147A>C | p.Gln716Pro | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/17 | 2217/2487 | 2147/2223 | 716/740 | chr2 | 26455214 | ||
chr2:26455220
|
A | G | 1 | a0020 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.2153A>G | p.Tyr718Cys | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/17 | 2223/2487 | 2153/2223 | 718/740 | chr2 | 26455220 | ||
chr2:26456494
|
G | A | 1 | a0010 | 4 | HG00639.hp1 HG00642.hp2 HG01515.hp1 others(1): Show |
missense_variant | MODERATE | c.2200G>A | p.Val734Met | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 17/17 | 2270/2487 | 2200/2223 | 734/740 | chr2 | 26456494 | ||
chr2:26456517
|
A | C | 1 | a0000 | 1 | HG03225.hp1 | stop_lost | HIGH | c.2223A>C | p.Ter741Cysext*? | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 17/17 | 2293/2487 | 2223/2223 | 741/740 | chr2 | 26456517 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26402025
|
G | C | 1 | a0009c0010 | 4 | HG00738.hp1 HG02145.hp1 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.36G>C | p.Pro12Pro | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/17 | 106/2487 | 36/2223 | 12/740 | chr2 | 26402025 | ||
chr2:26414392
|
T | C | 1 | a0002c0018 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.204T>C | p.Asp68Asp | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/17 | 274/2487 | 204/2223 | 68/740 | chr2 | 26414392 | ||
chr2:26424409
|
T | G | 9 | a0000c0021a0001c0001a0003c0005others(6): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
synonymous_variant | LOW | c.495T>G | p.Ala165Ala | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/17 | 565/2487 | 495/2223 | 165/740 | chr2 | 26424409 | ||
chr2:26444911
|
C | T | 5 | a0000c0021a0006c0008a0007c0009others(2): Show | 27 | HG00408.hp1 HG00609.hp2 HG01243.hp2 others(24): Show |
synonymous_variant | LOW | c.1359C>T | p.Ser453Ser | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/17 | 1429/2487 | 1359/2223 | 453/740 | chr2 | 26444911 | ||
chr2:26453340
|
G | A | 3 | a0008c0011a0012c0014a0013c0017 | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
synonymous_variant | LOW | c.1710G>A | p.Ala570Ala | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/17 | 1780/2487 | 1710/2223 | 570/740 | chr2 | 26453340 | ||
chr2:26453454
|
G | A | 1 | a0001c0016 | 3 | HG02486.hp1 HG02818.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.1824G>A | p.Glu608Glu | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/17 | 1894/2487 | 1824/2223 | 608/740 | chr2 | 26453454 | ||
chr2:26454728
|
A | G | 2 | a0008c0011a0013c0017 | 5 | HG01891.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.2001A>G | p.Thr667Thr | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 15/17 | 2071/2487 | 2001/2223 | 667/740 | chr2 | 26454728 | ||
chr2:26455137
|
C | T | 1 | a0019c0027 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.2070C>T | p.Val690Val | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/17 | 2140/2487 | 2070/2223 | 690/740 | chr2 | 26455137 | ||
chr2:26455143
|
C | T | 1 | a0003c0025 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.2076C>T | p.Thr692Thr | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/17 | 2146/2487 | 2076/2223 | 692/740 | chr2 | 26455143 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26401921
|
T | A | 1 | a0002c0002t0006 | 1 | NA18946.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/17 | 69 | chr2 | 26401921 | |||||
chr2:26401950
|
T | C | 2 | a0008c0011t0005a0013c0017t0005 | 2 | HG02922.hp1 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-40T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/17 | 40 | chr2 | 26401950 | |||||
chr2:26401975
|
C | T | 4 | a0001c0001t0002a0001c0007t0002a0003c0004t0002others(1): Show | 26 | HG01168.hp2 HG01169.hp2 HG02258.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-15C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/17 | 15 | chr2 | 26401975 | |||||
chr2:26456526
|
G | A | 1 | a0001c0001t0004 | 6 | HG00099.hp1 HG00733.hp2 HG01515.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 17/17 | 9 | chr2 | 26456526 | |||||
chr2:26456562
|
G | A | 6 | a0000c0021t0003a0001c0001t0003a0001c0007t0003others(3): Show | 25 | HG01496.hp1 HG01884.hp1 HG02280.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*45G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 17/17 | 45 | chr2 | 26456562 | |||||
chr2:26456627
|
C | A | 1 | a0001c0001t0007 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*110C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 17/17 | 110 | chr2 | 26456627 | |||||
chr2:26456647
|
T | G | 1 | a0008c0012t0008 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*130T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 17/17 | 130 | chr2 | 26456647 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26402169
|
G | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0023a0003c0004t0001g0024others(4): Show | 7 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+25G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26402169 | ||||||
chr2:26402174
|
C | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 66 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.155+30C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26402174 | ||||||
chr2:26402270
|
C | T | 1 | a0014c0019t0001g0365 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.155+126C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26402270 | ||||||
chr2:26402933
|
T | A | 1 | a0002c0002t0001g0083 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.155+789T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26402933 | ||||||
chr2:26403125
|
C | G | 9 | a0003c0004t0001g0360a0003c0005t0003g0358a0003c0005t0003g0359others(6): Show | 9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.155+981C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26403125 | ||||||
chr2:26403177
|
T | C | 1 | a0003c0004t0003g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.155+1033T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26403177 | ||||||
chr2:26403297
|
G | A | 2 | a0002c0002t0001g0084a0002c0002t0001g0085 | 2 | HG02523.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.155+1153G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26403297 | ||||||
chr2:26403401
|
C | T | 2 | a0002c0002t0001g0354a0002c0002t0001g0355 | 2 | HG02080.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.155+1257C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26403401 | ||||||
chr2:26403621
|
C | G | 46 | a0000c0021t0003g0327a0001c0001t0001g0017a0001c0001t0001g0315others(43): Show | 47 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.155+1477C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26403621 | ||||||
chr2:26403667
|
C | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 67 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.155+1523C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26403667 | ||||||
chr2:26403795
|
C | CA | 214 | a0000c0021t0003g0327a0001c0001t0001g0026a0001c0001t0001g0027others(211): Show | 222 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.155+1671dupA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26403795 | |||||
chr2:26403795
|
C | CAA | 7 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0004g0090others(4): Show | 7 | HG01081.hp1 HG01169.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.155+1670_155+1671d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26403795 | |||||
chr2:26403795
|
CA | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0002g0304others(4): Show | 8 | HG00558.hp2 HG01243.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.155+1671delA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26403795 | |||||
chr2:26403968
|
C | T | 44 | a0000c0021t0003g0327a0001c0001t0001g0017a0001c0001t0001g0315others(41): Show | 45 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.155+1824C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26403968 | ||||||
chr2:26403973
|
G | A | 9 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0007t0001g0270others(6): Show | 9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.155+1829G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26403973 | ||||||
chr2:26404015
|
G | A | 1 | a0003c0004t0001g0029 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.155+1871G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404015 | ||||||
chr2:26404055
|
G | A | 9 | a0003c0004t0001g0360a0003c0005t0003g0358a0003c0005t0003g0359others(6): Show | 9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.155+1911G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404055 | ||||||
chr2:26404113
|
T | A | 4 | a0002c0002t0001g0086a0002c0002t0001g0093a0002c0002t0001g0094others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.155+1969T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404113 | ||||||
chr2:26404279
|
G | A | 98 | a0001c0007t0001g0144a0002c0002t0001g0001a0002c0002t0001g0002others(95): Show | 106 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.155+2135G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404279 | ||||||
chr2:26404408
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG01106.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.155+2264C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404408 | ||||||
chr2:26404451
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0022c0020t0001g0028 | 3 | HG01168.hp1 HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.155+2307A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404451 | ||||||
chr2:26404452
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG01069.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.155+2308G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404452 | ||||||
chr2:26404459
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.155+2315A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404459 | ||||||
chr2:26404472
|
T | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0023a0003c0004t0001g0024others(4): Show | 7 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+2328T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404472 | ||||||
chr2:26404655
|
T | G | 324 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.155+2511T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404655 | ||||||
chr2:26404821
|
T | C | 215 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0089others(212): Show | 223 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.155+2677T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26404821 | ||||||
chr2:26405018
|
G | T | 9 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0007t0001g0270others(6): Show | 9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.155+2874G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405018 | ||||||
chr2:26405029
|
A | G | 324 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.155+2885A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405029 | ||||||
chr2:26405041
|
C | T | 7 | a0003c0004t0001g0259a0003c0004t0001g0260a0003c0004t0001g0262others(4): Show | 7 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.155+2897C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405041 | ||||||
chr2:26405072
|
C | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 67 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.155+2928C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405072 | ||||||
chr2:26405232
|
C | T | 73 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0204others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.155+3088C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405232 | ||||||
chr2:26405399
|
A | G | 1 | a0007c0009t0001g0191 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.155+3255A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405399 | ||||||
chr2:26405642
|
A | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 65 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.155+3498A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405642 | ||||||
chr2:26405645
|
G | A | 1 | a0002c0002t0001g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.155+3501G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405645 | ||||||
chr2:26405653
|
C | CT | 20 | a0001c0001t0001g0017a0001c0001t0001g0330a0001c0001t0001g0332others(17): Show | 21 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.155+3533dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26405653 | |||||
chr2:26405653
|
C | CTT | 9 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0003g0352others(6): Show | 9 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.155+3532_155+3533d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26405653 | |||||
chr2:26405653
|
CT | C | 175 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0026others(172): Show | 183 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.155+3533delT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26405653 | |||||
chr2:26405653
|
CTT | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 68 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.155+3532_155+3533d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26405653 | |||||
chr2:26405654
|
T | A | 2 | a0008c0011t0005g0310a0013c0017t0005g0309 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.155+3510T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405654 | ||||||
chr2:26405656
|
T | A | 2 | a0008c0011t0005g0310a0013c0017t0005g0309 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.155+3512T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405656 | ||||||
chr2:26405658
|
T | A | 2 | a0008c0011t0005g0310a0013c0017t0005g0309 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.155+3514T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405658 | ||||||
chr2:26405660
|
T | A | 2 | a0008c0011t0005g0310a0013c0017t0005g0309 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.155+3516T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405660 | ||||||
chr2:26405683
|
C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 65 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.155+3539C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405683 | ||||||
chr2:26405785
|
C | T | 1 | a0002c0002t0001g0167 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.155+3641C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405785 | ||||||
chr2:26405995
|
G | C | 40 | a0001c0001t0001g0017a0001c0001t0001g0315a0001c0001t0001g0330others(37): Show | 41 | HG00733.hp1 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.155+3851G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26405995 | ||||||
chr2:26406259
|
CAT | C | 5 | a0003c0004t0001g0360a0003c0025t0001g0356a0011c0015t0001g0357others(2): Show | 5 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.155+4116_155+4117d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26406259 | ||||||
chr2:26406546
|
C | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0023a0003c0004t0001g0024others(4): Show | 7 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+4402C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26406546 | ||||||
chr2:26406572
|
T | G | 324 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.155+4428T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26406572 | ||||||
chr2:26406637
|
G | A | 2 | a0004c0003t0001g0193a0004c0003t0001g0194 | 2 | HG03669.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.155+4493G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26406637 | ||||||
chr2:26406637
|
G | T | 7 | a0003c0004t0001g0259a0003c0004t0001g0260a0003c0004t0001g0262others(4): Show | 7 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.155+4493G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26406637 | ||||||
chr2:26406666
|
C | T | 1 | a0004c0003t0001g0252 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.155+4522C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26406666 | ||||||
chr2:26406698
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0303 | 3 | NA18952.hp2 NA18986.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.155+4554C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26406698 | ||||||
chr2:26406705
|
CCTT | C | 9 | a0003c0004t0001g0360a0003c0005t0003g0358a0003c0005t0003g0359others(6): Show | 9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.155+4564_155+4566d others(5): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26406705 | |||||
chr2:26406813
|
C | CT | 44 | a0001c0001t0001g0039a0001c0001t0002g0302a0001c0001t0003g0038others(41): Show | 45 | HG00408.hp1 HG00609.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.155+4691dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26406813 | |||||
chr2:26406813
|
C | CTT | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 90 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(87): Show |
intron_variant | MODIFIER | c.155+4690_155+4691d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26406813 | |||||
chr2:26406813
|
C | CTTT | 12 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0031others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.155+4689_155+4691d others(5): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26406813 | |||||
chr2:26406813
|
CT | C | 6 | a0001c0001t0002g0304a0002c0002t0001g0098a0002c0002t0001g0195others(3): Show | 6 | HG01515.hp1 HG01975.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+4691delT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26406813 | |||||
chr2:26406813
|
CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(4): Show | 7 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+4683_155+4691d others(11): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26406813 | |||||
chr2:26406826
|
T | TTC | 5 | a0001c0001t0001g0017a0001c0001t0001g0330a0001c0001t0001g0332others(2): Show | 6 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.155+4683_155+4684i others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26406826 | |||||
chr2:26406850
|
C | A | 1 | a0004c0003t0001g0197 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.155+4706C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26406850 | ||||||
chr2:26406861
|
G | A | 3 | a0002c0002t0001g0098a0002c0002t0001g0099a0002c0002t0001g0160 | 3 | NA18957.hp1 NA18959.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.155+4717G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26406861 | ||||||
chr2:26407078
|
G | A | 9 | a0003c0004t0001g0360a0003c0005t0003g0358a0003c0005t0003g0359others(6): Show | 9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.155+4934G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407078 | ||||||
chr2:26407231
|
C | T | 6 | a0002c0002t0001g0301a0003c0005t0001g0274a0003c0005t0001g0298others(3): Show | 6 | HG00558.hp2 NA18942.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+5087C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407231 | ||||||
chr2:26407406
|
A | G | 1 | a0003c0004t0001g0262 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.155+5262A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407406 | ||||||
chr2:26407521
|
A | T | 87 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0089others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.155+5377A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407521 | ||||||
chr2:26407561
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.155+5417G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407561 | ||||||
chr2:26407671
|
T | G | 1 | a0001c0001t0001g0040 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.155+5527T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407671 | ||||||
chr2:26407696
|
A | G | 1 | a0003c0004t0001g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.155+5552A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407696 | ||||||
chr2:26407725
|
C | T | 9 | a0001c0001t0001g0347a0001c0001t0003g0352a0001c0007t0001g0348others(6): Show | 9 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.155+5581C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407725 | ||||||
chr2:26407830
|
C | T | 1 | a0004c0003t0001g0252 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.155+5686C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407830 | ||||||
chr2:26407831
|
A | C | 1 | a0001c0007t0001g0270 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.155+5687A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407831 | ||||||
chr2:26407889
|
C | T | 1 | a0002c0002t0001g0159 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.155+5745C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26407889 | ||||||
chr2:26408072
|
G | T | 2 | a0002c0002t0001g0157a0002c0002t0001g0158 | 2 | HG02015.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.155+5928G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26408072 | ||||||
chr2:26408300
|
C | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 49 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.156-6044C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26408300 | ||||||
chr2:26408631
|
C | T | 23 | a0001c0007t0001g0144a0002c0002t0001g0002a0002c0002t0001g0011others(20): Show | 26 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.156-5713C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26408631 | ||||||
chr2:26408678
|
C | T | 3 | a0003c0004t0001g0328a0003c0004t0001g0329a0019c0027t0001g0344 | 3 | HG00642.hp1 HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.156-5666C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26408678 | ||||||
chr2:26408702
|
C | T | 1 | a0001c0001t0007g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.156-5642C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26408702 | ||||||
chr2:26408836
|
C | T | 1 | a0001c0001t0004g0250 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.156-5508C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26408836 | ||||||
chr2:26408853
|
C | T | 1 | a0015c0031t0001g0364 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.156-5491C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26408853 | ||||||
chr2:26408882
|
C | G | 30 | a0004c0003t0001g0012a0004c0003t0001g0227a0004c0003t0001g0228others(27): Show | 30 | HG00438.hp2 HG01255.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.156-5462C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26408882 | ||||||
chr2:26408974
|
C | T | 24 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0268others(21): Show | 26 | HG01168.hp2 HG01169.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.156-5370C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26408974 | ||||||
chr2:26409008
|
G | C | 11 | a0003c0004t0001g0360a0003c0005t0003g0358a0003c0005t0003g0359others(8): Show | 11 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.156-5336G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409008 | ||||||
chr2:26409009
|
T | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0023a0003c0004t0001g0024others(4): Show | 7 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.156-5335T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409009 | ||||||
chr2:26409055
|
C | A | 1 | a0002c0002t0001g0100 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.156-5289C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409055 | ||||||
chr2:26409102
|
T | G | 1 | a0005c0006t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.156-5242T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409102 | ||||||
chr2:26409123
|
A | G | 348 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(345): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.156-5221A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409123 | ||||||
chr2:26409206
|
C | T | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(282): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.156-5138C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409206 | ||||||
chr2:26409225
|
T | C | 349 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(346): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.156-5119T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409225 | ||||||
chr2:26409454
|
T | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0023a0003c0004t0001g0024others(4): Show | 7 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.156-4890T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409454 | ||||||
chr2:26409509
|
T | A | 9 | a0003c0004t0001g0360a0003c0005t0003g0358a0003c0005t0003g0359others(6): Show | 9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.156-4835T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409509 | ||||||
chr2:26409767
|
G | A | 2 | a0008c0011t0005g0310a0013c0017t0005g0309 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.156-4577G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409767 | ||||||
chr2:26409904
|
A | G | 11 | a0003c0004t0001g0360a0003c0005t0003g0358a0003c0005t0003g0359others(8): Show | 11 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.156-4440A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26409904 | ||||||
chr2:26410076
|
G | A | 63 | a0000c0021t0003g0327a0001c0001t0001g0017a0001c0001t0001g0315others(60): Show | 66 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.156-4268G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410076 | ||||||
chr2:26410146
|
T | G | 1 | a0002c0002t0001g0007 | 2 | NA18961.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.156-4198T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410146 | ||||||
chr2:26410245
|
A | ATAT | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 75 | HG00408.hp2 HG00639.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.156-4063_156-4061d others(5): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26410245 | |||||
chr2:26410245
|
A | ATATTAT | 47 | a0001c0001t0001g0027a0001c0001t0001g0076a0001c0001t0001g0078others(44): Show | 47 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.156-4066_156-4061d others(8): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26410245 | |||||
chr2:26410245
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.156-4099A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410245 | ||||||
chr2:26410245
|
ATAT | A | 118 | a0000c0021t0003g0327a0001c0001t0001g0041a0001c0001t0001g0330others(115): Show | 124 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.156-4063_156-4061d others(5): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26410245 | |||||
chr2:26410245
|
ATATTAT | A | 4 | a0001c0001t0002g0282a0002c0002t0001g0101a0003c0004t0001g0029others(1): Show | 4 | HG01934.hp1 HG02559.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-4066_156-4061d others(8): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26410245 | |||||
chr2:26410245
|
ATATTATT others(2): Show |
A | 4 | a0003c0004t0001g0328a0003c0004t0001g0329a0011c0015t0001g0016others(1): Show | 5 | HG00642.hp1 HG01109.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-4069_156-4061d others(11): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26410245 | |||||
chr2:26410245
|
ATATTATT others(5): Show |
A | 7 | a0003c0004t0001g0360a0003c0025t0001g0356a0008c0011t0005g0310others(4): Show | 7 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.156-4072_156-4061d others(14): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26410245 | |||||
chr2:26410294
|
G | A | 18 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(15): Show | 18 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.156-4050G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410294 | ||||||
chr2:26410341
|
G | A | 2 | a0008c0011t0005g0310a0013c0017t0005g0309 | 2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.156-4003G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410341 | ||||||
chr2:26410428
|
T | C | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(280): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.156-3916T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410428 | ||||||
chr2:26410428
|
T | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02145.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.156-3916T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410428 | ||||||
chr2:26410483
|
G | A | 1 | a0002c0002t0001g0141 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.156-3861G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410483 | ||||||
chr2:26410518
|
C | T | 7 | a0001c0007t0001g0270a0001c0007t0003g0269a0003c0004t0001g0326others(4): Show | 7 | HG00733.hp1 HG01167.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.156-3826C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410518 | ||||||
chr2:26410554
|
G | A | 1 | a0018c0023t0001g0198 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.156-3790G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410554 | ||||||
chr2:26410565
|
C | A | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-3779C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410565 | ||||||
chr2:26410635
|
G | A | 274 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.156-3709G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410635 | ||||||
chr2:26410769
|
A | T | 1 | a0000c0021t0003g0327 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.156-3575A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410769 | ||||||
chr2:26410811
|
G | GAAACAAA others(13): Show |
1 | a0008c0011t0005g0310 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.156-3517_156-3498d others(22): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26410811 | |||||
chr2:26410824
|
A | G | 1 | a0003c0004t0003g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.156-3520A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410824 | ||||||
chr2:26410827
|
C | A | 1 | a0001c0001t0002g0306 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.156-3517C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26410827 | ||||||
chr2:26410827
|
C | CAACAA | 58 | a0001c0001t0001g0017a0001c0001t0001g0315a0001c0001t0001g0330others(55): Show | 61 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.156-3499_156-3495d others(7): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26410827 | |||||
chr2:26411000
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0003c0004t0001g0024others(1): Show | 4 | HG02486.hp2 HG03209.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-3344C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411000 | ||||||
chr2:26411204
|
C | T | 2 | a0008c0012t0001g0257a0008c0012t0001g0258 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.156-3140C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411204 | ||||||
chr2:26411344
|
G | A | 10 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(7): Show | 10 | HG02622.hp1 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.156-3000G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411344 | ||||||
chr2:26411398
|
G | C | 2 | a0003c0004t0003g0264a0003c0004t0003g0265 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.156-2946G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411398 | ||||||
chr2:26411444
|
C | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.156-2900C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411444 | ||||||
chr2:26411498
|
A | G | 1 | a0022c0020t0001g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.156-2846A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411498 | ||||||
chr2:26411513
|
A | G | 7 | a0002c0002t0001g0086a0002c0002t0001g0093a0002c0002t0001g0094others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.156-2831A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411513 | ||||||
chr2:26411561
|
TAAGTTAA others(3): Show |
T | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.156-2782_156-2773d others(12): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411561 | ||||||
chr2:26411723
|
G | C | 5 | a0003c0005t0003g0261a0003c0005t0003g0358a0003c0005t0003g0359others(2): Show | 5 | HG01496.hp1 HG02572.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.156-2621G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411723 | ||||||
chr2:26411729
|
G | A | 2 | a0004c0003t0001g0236a0004c0003t0001g0252 | 2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.156-2615G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411729 | ||||||
chr2:26411766
|
C | G | 34 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0334others(31): Show | 34 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.156-2578C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411766 | ||||||
chr2:26411795
|
T | TA | 50 | a0001c0001t0001g0017a0001c0001t0001g0332a0001c0001t0001g0347others(47): Show | 54 | HG00558.hp2 HG00741.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.156-2535dupA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26411795 | |||||
chr2:26411795
|
TA | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.156-2535delA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26411795 | |||||
chr2:26411841
|
G | T | 19 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(16): Show | 19 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.156-2503G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411841 | ||||||
chr2:26411882
|
G | C | 1 | a0017c0022t0001g0173 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.156-2462G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26411882 | ||||||
chr2:26412048
|
C | G | 164 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.156-2296C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26412048 | ||||||
chr2:26412223
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.156-2121G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26412223 | ||||||
chr2:26412460
|
A | C | 261 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.156-1884A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26412460 | ||||||
chr2:26412503
|
T | A | 164 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.156-1841T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26412503 | ||||||
chr2:26412541
|
C | T | 25 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(22): Show | 26 | HG00733.hp1 HG00741.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.156-1803C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26412541 | ||||||
chr2:26412574
|
G | A | 69 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(66): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.156-1770G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26412574 | ||||||
chr2:26412637
|
A | G | 1 | a0002c0002t0001g0127 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.156-1707A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26412637 | ||||||
chr2:26412846
|
C | T | 86 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0026others(83): Show | 86 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.156-1498C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26412846 | ||||||
chr2:26412996
|
G | A | 49 | a0002c0002t0001g0195a0002c0002t0001g0203a0002c0002t0001g0301others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.156-1348G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26412996 | ||||||
chr2:26413019
|
C | T | 3 | a0009c0010t0001g0013a0009c0010t0001g0267a0009c0010t0001g0281 | 4 | HG00738.hp1 HG02145.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-1325C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26413019 | ||||||
chr2:26413112
|
T | C | 1 | a0003c0025t0001g0356 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.156-1232T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26413112 | ||||||
chr2:26413218
|
C | T | 122 | a0001c0001t0001g0347a0001c0007t0001g0144a0001c0007t0001g0270others(119): Show | 131 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.156-1126C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26413218 | ||||||
chr2:26413270
|
T | C | 1 | a0003c0005t0003g0331 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.156-1074T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26413270 | ||||||
chr2:26413302
|
C | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.156-1042C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26413302 | ||||||
chr2:26413395
|
A | G | 4 | a0002c0002t0001g0140a0007c0009t0001g0185a0007c0009t0001g0186others(1): Show | 4 | HG00609.hp2 NA18940.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-949A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26413395 | ||||||
chr2:26413521
|
T | C | 13 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(10): Show | 13 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.156-823T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26413521 | ||||||
chr2:26413522
|
A | G | 86 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0026others(83): Show | 86 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.156-822A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26413522 | ||||||
chr2:26413749
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.156-595T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26413749 | ||||||
chr2:26413957
|
A | C | 2 | a0011c0015t0001g0016a0011c0015t0001g0357 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.156-387A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26413957 | ||||||
chr2:26414051
|
C | T | 1 | a0003c0005t0001g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.156-293C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26414051 | ||||||
chr2:26414110
|
G | T | 13 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(10): Show | 13 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.156-234G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26414110 | ||||||
chr2:26414115
|
C | CATT | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 78 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.156-201_156-199dup others(3): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26414115 | |||||
chr2:26414115
|
C | CATTATT | 83 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0039others(80): Show | 83 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.156-204_156-199dup others(6): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26414115 | |||||
chr2:26414115
|
C | CATTATTA others(2): Show |
14 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0041others(11): Show | 14 | HG00639.hp2 HG01074.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.156-207_156-199dup others(9): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26414115 | |||||
chr2:26414115
|
C | CATTATTA others(5): Show |
3 | a0001c0001t0004g0213a0001c0001t0007g0050a0003c0005t0001g0019 | 3 | HG00733.hp2 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.156-210_156-199dup others(12): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26414115 | |||||
chr2:26414115
|
C | CATTATTA others(8): Show |
3 | a0001c0001t0001g0047a0001c0001t0001g0091a0001c0001t0004g0212 | 3 | HG01081.hp1 HG01891.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.156-213_156-199dup others(15): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26414115 | |||||
chr2:26414115
|
C | CATTATTA others(11): Show |
6 | a0000c0021t0003g0327a0001c0001t0001g0211a0001c0001t0001g0224others(3): Show | 6 | HG00099.hp1 HG01433.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-216_156-199dup others(18): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26414115 | |||||
chr2:26414115
|
C | CATTATTA others(14): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0332a0003c0005t0003g0331 | 4 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-219_156-199dup others(21): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26414115 | |||||
chr2:26414115
|
C | CATTATTA others(17): Show |
1 | a0001c0001t0001g0046 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.156-222_156-199dup others(24): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26414115 | |||||
chr2:26414115
|
CATT | C | 43 | a0001c0001t0001g0347a0001c0001t0002g0292a0001c0007t0001g0270others(40): Show | 44 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(41): Show |
intron_variant | MODIFIER | c.156-201_156-199del others(3): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26414115 | |||||
chr2:26414115
|
CATTATT | C | 106 | a0001c0007t0001g0144a0002c0002t0001g0001a0002c0002t0001g0002others(103): Show | 114 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.156-204_156-199del others(6): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 26414115 | |||||
chr2:26414200
|
C | T | 110 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0026others(107): Show | 112 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.156-144C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26414200 | ||||||
chr2:26414254
|
G | A | 2 | a0011c0015t0001g0016a0011c0015t0001g0357 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.156-90G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26414254 | ||||||
chr2:26414304
|
T | C | 27 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(24): Show | 28 | HG00733.hp1 HG00741.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.156-40T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 1/16 | chr2 | 26414304 | ||||||
chr2:26414618
|
G | A | 3 | a0002c0002t0001g0084a0002c0002t0001g0085a0002c0002t0001g0105 | 3 | HG00423.hp1 HG02523.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.243+187G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26414618 | ||||||
chr2:26414927
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.243+496G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26414927 | ||||||
chr2:26414942
|
C | T | 6 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0004t0001g0360others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+511C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26414942 | ||||||
chr2:26415197
|
C | T | 50 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(47): Show | 51 | HG00733.hp1 HG00741.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.243+766C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26415197 | ||||||
chr2:26415270
|
T | C | 13 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(10): Show | 13 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.243+839T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26415270 | ||||||
chr2:26415356
|
G | A | 1 | a0002c0002t0001g0157 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.243+925G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26415356 | ||||||
chr2:26415425
|
T | C | 1 | a0002c0002t0001g0159 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.243+994T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26415425 | ||||||
chr2:26415454
|
T | C | 186 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.243+1023T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26415454 | ||||||
chr2:26415545
|
T | C | 3 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0003g0352 | 3 | HG01074.hp2 HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.243+1114T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26415545 | ||||||
chr2:26415703
|
G | T | 1 | a0002c0002t0001g0161 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.243+1272G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26415703 | ||||||
chr2:26415760
|
C | T | 7 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(4): Show | 7 | HG02622.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+1329C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26415760 | ||||||
chr2:26415785
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0023a0003c0005t0001g0018others(3): Show | 6 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+1354G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26415785 | ||||||
chr2:26415829
|
G | A | 1 | a0002c0002t0001g0007 | 2 | NA18961.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.243+1398G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26415829 | ||||||
chr2:26415935
|
C | CA | 15 | a0001c0001t0001g0055a0001c0001t0001g0089a0001c0001t0004g0090others(12): Show | 16 | HG00438.hp1 HG00642.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+1525dupA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26415935 | |||||
chr2:26415935
|
CA | C | 144 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0023others(141): Show | 148 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.243+1525delA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26415935 | |||||
chr2:26415935
|
CAA | C | 23 | a0000c0021t0003g0327a0001c0001t0001g0334a0001c0001t0001g0335others(20): Show | 23 | HG00741.hp2 HG02015.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.243+1524_243+1525d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26415935 | |||||
chr2:26416013
|
T | C | 1 | a0003c0004t0001g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.243+1582T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416013 | ||||||
chr2:26416115
|
A | C | 50 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(47): Show | 51 | HG00733.hp1 HG00741.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.243+1684A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416115 | ||||||
chr2:26416149
|
A | G | 2 | a0008c0012t0001g0257a0008c0012t0001g0258 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.243+1718A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416149 | ||||||
chr2:26416164
|
C | T | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+1733C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416164 | ||||||
chr2:26416272
|
C | T | 1 | a0003c0004t0003g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.243+1841C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416272 | ||||||
chr2:26416339
|
C | A | 27 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(24): Show | 28 | HG00733.hp1 HG00741.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.243+1908C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416339 | ||||||
chr2:26416384
|
C | A | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.243+1953C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416384 | ||||||
chr2:26416405
|
G | T | 185 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.243+1974G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416405 | ||||||
chr2:26416498
|
A | C | 1 | a0003c0004t0001g0314 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.243+2067A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416498 | ||||||
chr2:26416517
|
T | A | 1 | a0001c0001t0004g0075 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.243+2086T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416517 | ||||||
chr2:26416578
|
G | A | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.243+2147G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416578 | ||||||
chr2:26416818
|
A | G | 1 | a0004c0003t0001g0234 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.243+2387A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416818 | ||||||
chr2:26416859
|
C | T | 1 | a0002c0002t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.243+2428C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416859 | ||||||
chr2:26416911
|
C | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.243+2480C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26416911 | ||||||
chr2:26417040
|
C | T | 2 | a0004c0003t0001g0232a0004c0003t0001g0233 | 2 | HG02132.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.243+2609C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417040 | ||||||
chr2:26417098
|
C | T | 6 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0004t0001g0360others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+2667C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417098 | ||||||
chr2:26417253
|
T | C | 1 | a0002c0002t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.243+2822T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417253 | ||||||
chr2:26417348
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.243+2917C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417348 | ||||||
chr2:26417511
|
C | T | 27 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(24): Show | 28 | HG00733.hp1 HG00741.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.243+3080C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417511 | ||||||
chr2:26417513
|
G | A | 1 | a0008c0011t0005g0310 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.243+3082G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417513 | ||||||
chr2:26417537
|
C | T | 1 | a0006c0008t0001g0184 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.243+3106C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417537 | ||||||
chr2:26417620
|
C | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0023a0003c0005t0001g0018others(3): Show | 6 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+3189C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417620 | ||||||
chr2:26417755
|
C | A | 5 | a0001c0001t0001g0211a0001c0001t0004g0090a0001c0001t0004g0192others(2): Show | 5 | HG00099.hp1 HG02698.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+3324C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417755 | ||||||
chr2:26417794
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0003g0209 | 2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.243+3363C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417794 | ||||||
chr2:26417810
|
T | G | 8 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.243+3379T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417810 | ||||||
chr2:26417818
|
T | A | 1 | a0008c0012t0001g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.243+3387T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417818 | ||||||
chr2:26417847
|
T | A | 7 | a0001c0007t0001g0092a0001c0007t0001g0251a0003c0005t0003g0261others(4): Show | 7 | HG01496.hp1 HG02572.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+3416T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417847 | ||||||
chr2:26417912
|
C | T | 1 | a0002c0002t0001g0139 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.244-3376C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417912 | ||||||
chr2:26417913
|
G | A | 235 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.244-3375G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417913 | ||||||
chr2:26417993
|
A | T | 1 | a0008c0012t0001g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.244-3295A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26417993 | ||||||
chr2:26418161
|
C | T | 2 | a0010c0013t0001g0196a0010c0013t0001g0223 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.244-3127C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418161 | ||||||
chr2:26418316
|
A | T | 13 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(10): Show | 13 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.244-2972A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418316 | ||||||
chr2:26418342
|
C | T | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2946C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418342 | ||||||
chr2:26418536
|
T | C | 2 | a0011c0015t0001g0016a0011c0015t0001g0357 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.244-2752T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418536 | ||||||
chr2:26418540
|
T | TTATAAAT others(31): Show |
3 | a0002c0002t0001g0103a0002c0002t0001g0104a0002c0002t0001g0161 | 3 | NA18953.hp2 NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.244-2723_244-2686d others(40): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418540 | |||||
chr2:26418540
|
TTATAAAT others(58): Show |
T | 2 | a0008c0012t0001g0257a0008c0012t0001g0258 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.244-2730_244-2666d others(67): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418540 | |||||
chr2:26418555
|
AATTTATA others(15): Show |
A | 10 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(7): Show | 11 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.244-2730_244-2709d others(24): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418555 | |||||
chr2:26418556
|
AT | A | 18 | a0001c0007t0002g0293a0001c0007t0002g0295a0003c0004t0001g0024others(15): Show | 18 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.244-2729delT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418556 | |||||
chr2:26418558
|
TTA | T | 19 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(16): Show | 19 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.244-2723_244-2722d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418558 | |||||
chr2:26418560
|
A | ATATATAA others(103): Show |
1 | a0001c0007t0001g0251 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.244-2708_244-2707i others(112): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418560 | |||||
chr2:26418560
|
A | ATATATAA others(103): Show |
1 | a0001c0007t0001g0092 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.244-2708_244-2707i others(112): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418560 | |||||
chr2:26418560
|
A | ATATATAA others(29): Show |
5 | a0003c0005t0003g0261a0003c0005t0003g0358a0003c0005t0003g0359others(2): Show | 5 | HG01496.hp1 HG02572.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-2714_244-2679d others(38): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418560 | |||||
chr2:26418563
|
T | A | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2725T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418563 | ||||||
chr2:26418565
|
TAA | T | 4 | a0000c0021t0003g0327a0001c0001t0001g0017a0001c0001t0001g0332others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-2722_244-2721d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418565 | ||||||
chr2:26418566
|
A | T | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2722A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418566 | ||||||
chr2:26418574
|
T | A | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2714T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418574 | ||||||
chr2:26418574
|
TTATA | T | 6 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0004t0001g0360others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-2709_244-2706d others(6): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418574 | |||||
chr2:26418575
|
T | TATATATA others(20): Show |
1 | a0004c0003t0001g0218 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.244-2692_244-2666d others(29): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418575 | |||||
chr2:26418575
|
TATATATA others(20): Show |
T | 1 | a0002c0002t0006g0097 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.244-2692_244-2666d others(29): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418575 | |||||
chr2:26418576
|
A | T | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2712A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418576 | ||||||
chr2:26418577
|
T | TAAATTAC | 7 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(4): Show | 7 | HG02622.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-2710_244-2709i others(9): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418577 | |||||
chr2:26418584
|
A | T | 7 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(4): Show | 7 | HG02622.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-2704A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418584 | ||||||
chr2:26418588
|
T | C | 6 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0004t0001g0360others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-2700T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418588 | ||||||
chr2:26418595
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.244-2693T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418595 | ||||||
chr2:26418596
|
T | A | 49 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.244-2692T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418596 | ||||||
chr2:26418602
|
A | T | 7 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(4): Show | 7 | HG02622.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-2686A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418602 | ||||||
chr2:26418603
|
A | T | 101 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(98): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.244-2685A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418603 | ||||||
chr2:26418604
|
T | A | 6 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0004t0001g0360others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-2684T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418604 | ||||||
chr2:26418608
|
TA | T | 22 | a0001c0007t0002g0293a0001c0007t0002g0295a0003c0004t0001g0024others(19): Show | 22 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.244-2677delA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418608 | |||||
chr2:26418610
|
A | T | 6 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0004t0001g0360others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-2678A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418610 | ||||||
chr2:26418611
|
A | T | 10 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(7): Show | 11 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.244-2677A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418611 | ||||||
chr2:26418615
|
TATATA | T | 6 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0004t0001g0360others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-2666_244-2662d others(7): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418615 | |||||
chr2:26418618
|
A | T | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2670A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418618 | ||||||
chr2:26418620
|
A | AATATAAA others(20): Show |
3 | a0001c0001t0001g0225a0001c0001t0001g0315a0001c0001t0001g0330 | 3 | HG00639.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.244-2643_244-2642i others(29): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418620 | |||||
chr2:26418620
|
A | AATTTATA others(15): Show |
7 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(4): Show | 7 | HG02622.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-2666_244-2665i others(24): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418620 | |||||
chr2:26418620
|
A | T | 10 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(7): Show | 11 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.244-2668A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418620 | ||||||
chr2:26418623
|
A | T | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2665A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418623 | ||||||
chr2:26418626
|
A | T | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2662A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418626 | ||||||
chr2:26418629
|
T | A | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2659T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418629 | ||||||
chr2:26418631
|
T | A | 17 | a0001c0007t0001g0092a0001c0007t0001g0251a0003c0005t0003g0261others(14): Show | 18 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.244-2657T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418631 | ||||||
chr2:26418638
|
TTTATATA others(9): Show |
T | 11 | a0001c0001t0001g0027a0008c0011t0001g0323a0008c0011t0001g0324others(8): Show | 12 | HG00733.hp1 HG01167.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.244-2642_244-2627d others(18): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418638 | |||||
chr2:26418639
|
T | A | 11 | a0003c0004t0001g0024a0003c0004t0001g0314a0003c0004t0001g0316others(8): Show | 11 | HG01346.hp2 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.244-2649T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418639 | ||||||
chr2:26418645
|
A | T | 25 | a0001c0007t0002g0293a0001c0007t0002g0295a0003c0004t0001g0024others(22): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.244-2643A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418645 | ||||||
chr2:26418645
|
AAT | A | 4 | a0000c0021t0003g0327a0001c0001t0001g0017a0001c0001t0001g0332others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-2637_244-2636d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418645 | |||||
chr2:26418646
|
A | ATATATAA others(9): Show |
1 | a0007c0009t0001g0128 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.244-2630_244-2615d others(18): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418646 | |||||
chr2:26418646
|
A | T | 102 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0089others(99): Show | 104 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.244-2642A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418646 | ||||||
chr2:26418650
|
A | T | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2638A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418650 | ||||||
chr2:26418654
|
A | T | 4 | a0008c0012t0001g0257a0008c0012t0001g0258a0008c0012t0001g0343others(1): Show | 4 | HG02886.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-2634A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418654 | ||||||
chr2:26418662
|
T | A | 2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-2626T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418662 | ||||||
chr2:26418665
|
TATAAATT others(34): Show |
T | 2 | a0008c0012t0001g0257a0008c0012t0001g0258 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.244-2620_244-2580d others(43): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418665 | |||||
chr2:26418674
|
A | T | 23 | a0002c0002t0001g0010a0002c0002t0001g0098a0002c0002t0001g0099others(20): Show | 25 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.244-2614A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418674 | ||||||
chr2:26418677
|
A | T | 12 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(9): Show | 13 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.244-2611A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418677 | ||||||
chr2:26418688
|
T | A | 25 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(22): Show | 26 | HG00733.hp1 HG00741.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-2600T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418688 | ||||||
chr2:26418688
|
TATATATA others(20): Show |
T | 2 | a0003c0004t0001g0029a0003c0004t0003g0025 | 2 | HG01934.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.244-2572_244-2546d others(29): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418688 | |||||
chr2:26418704
|
T | A | 1 | a0002c0002t0001g0161 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.244-2584T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418704 | ||||||
chr2:26418705
|
T | A | 1 | a0001c0001t0001g0032 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.244-2583T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418705 | ||||||
chr2:26418716
|
A | T | 13 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(10): Show | 13 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.244-2572A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418716 | ||||||
chr2:26418717
|
T | A | 13 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(10): Show | 13 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.244-2571T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418717 | ||||||
chr2:26418717
|
TATATAAA others(20): Show |
T | 19 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(16): Show | 19 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.244-2555_244-2529d others(29): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26418717 | |||||
chr2:26418724
|
A | G | 23 | a0001c0007t0002g0293a0001c0007t0002g0295a0003c0004t0001g0024others(20): Show | 23 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.244-2564A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418724 | ||||||
chr2:26418731
|
T | A | 1 | a0008c0011t0005g0310 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.244-2557T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418731 | ||||||
chr2:26418743
|
T | A | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-2545T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418743 | ||||||
chr2:26418744
|
A | T | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-2544A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418744 | ||||||
chr2:26418763
|
T | A | 19 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(16): Show | 19 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.244-2525T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418763 | ||||||
chr2:26418917
|
C | G | 2 | a0003c0004t0001g0029a0003c0004t0003g0025 | 2 | HG01934.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.244-2371C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418917 | ||||||
chr2:26418976
|
C | T | 23 | a0001c0007t0002g0293a0001c0007t0002g0295a0003c0004t0001g0024others(20): Show | 23 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.244-2312C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418976 | ||||||
chr2:26418989
|
C | T | 22 | a0001c0007t0002g0293a0001c0007t0002g0295a0003c0004t0001g0024others(19): Show | 22 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.244-2299C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26418989 | ||||||
chr2:26419125
|
G | A | 1 | a0001c0001t0002g0302 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.244-2163G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26419125 | ||||||
chr2:26419184
|
C | T | 1 | a0004c0003t0001g0217 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.244-2104C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26419184 | ||||||
chr2:26419322
|
A | G | 70 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0077others(67): Show | 70 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.244-1966A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26419322 | ||||||
chr2:26419684
|
A | G | 6 | a0001c0007t0001g0270a0001c0007t0001g0348a0001c0007t0001g0349others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-1604A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26419684 | ||||||
chr2:26419715
|
C | T | 69 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(66): Show | 70 | HG00408.hp1 HG00609.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.244-1573C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26419715 | ||||||
chr2:26419819
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0007g0050 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.244-1469G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26419819 | ||||||
chr2:26419864
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG00741.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.244-1424G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26419864 | ||||||
chr2:26419964
|
C | T | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-1324C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26419964 | ||||||
chr2:26420225
|
C | T | 18 | a0001c0007t0002g0293a0001c0007t0002g0295a0003c0004t0001g0024others(15): Show | 18 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.244-1063C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26420225 | ||||||
chr2:26420268
|
C | T | 1 | a0003c0005t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.244-1020C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26420268 | ||||||
chr2:26420372
|
CCTGCCTC others(11): Show |
C | 70 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0077others(67): Show | 70 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.244-880_244-863del others(18): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26420372 | |||||
chr2:26420401
|
G | A | 4 | a0000c0021t0003g0327a0001c0001t0001g0017a0001c0001t0001g0332others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-887G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26420401 | ||||||
chr2:26420408
|
T | TCTGCCTC others(11): Show |
1 | a0001c0001t0001g0073 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.244-870_244-853dup others(18): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26420408 | |||||
chr2:26420500
|
C | A | 26 | a0001c0007t0001g0270a0001c0007t0001g0348a0001c0007t0001g0349others(23): Show | 27 | HG00733.hp1 HG00741.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.244-788C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26420500 | ||||||
chr2:26420757
|
TTTC | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.244-522_244-520del others(3): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26420757 | |||||
chr2:26420766
|
C | CT | 8 | a0001c0007t0002g0293a0001c0007t0002g0295a0003c0004t0001g0172others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.244-509dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26420766 | |||||
chr2:26420766
|
C | CTT | 6 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0004t0001g0360others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-510_244-509dup others(2): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26420766 | |||||
chr2:26420913
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.244-375G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26420913 | ||||||
chr2:26420946
|
T | G | 100 | a0001c0007t0001g0144a0002c0002t0001g0001a0002c0002t0001g0002others(97): Show | 108 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.244-342T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26420946 | ||||||
chr2:26420965
|
T | C | 1 | a0003c0005t0001g0275 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.244-323T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26420965 | ||||||
chr2:26420983
|
C | T | 1 | a0004c0003t0001g0236 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.244-305C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26420983 | ||||||
chr2:26420997
|
CAA | C | 13 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(10): Show | 13 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.244-289_244-288del others(2): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 26420997 | |||||
chr2:26421174
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.244-114T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 2/16 | chr2 | 26421174 | ||||||
chr2:26421449
|
T | C | 1 | a0002c0002t0001g0127 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.356+49T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26421449 | ||||||
chr2:26421467
|
C | T | 1 | a0003c0004t0001g0314 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.356+67C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26421467 | ||||||
chr2:26421557
|
C | CT | 73 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0055others(70): Show | 73 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.356+177dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 26421557 | |||||
chr2:26421557
|
CT | C | 10 | a0001c0001t0001g0308a0001c0007t0001g0144a0002c0002t0001g0145others(7): Show | 10 | HG00642.hp1 HG01257.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.356+177delT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 26421557 | |||||
chr2:26421558
|
T | TC | 20 | a0001c0007t0002g0293a0001c0007t0002g0295a0003c0004t0001g0024others(17): Show | 20 | HG01169.hp2 HG01346.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.356+158_356+159ins others(1): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26421558 | ||||||
chr2:26421559
|
T | C | 7 | a0001c0007t0001g0092a0001c0007t0001g0251a0003c0004t0002g0283others(4): Show | 7 | HG01168.hp2 HG02572.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.356+159T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26421559 | ||||||
chr2:26421560
|
T | C | 1 | a0003c0005t0003g0358 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.356+160T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26421560 | ||||||
chr2:26421561
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.356+161T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26421561 | ||||||
chr2:26421629
|
C | T | 7 | a0003c0004t0001g0328a0003c0004t0001g0329a0003c0004t0003g0264others(4): Show | 8 | HG00642.hp1 HG00738.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.356+229C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26421629 | ||||||
chr2:26421802
|
C | T | 2 | a0002c0002t0001g0354a0002c0002t0001g0355 | 2 | HG02080.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.356+402C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26421802 | ||||||
chr2:26422004
|
C | T | 27 | a0001c0007t0001g0092a0001c0007t0001g0251a0001c0007t0002g0293others(24): Show | 27 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.356+604C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26422004 | ||||||
chr2:26422207
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0023a0003c0005t0001g0018others(3): Show | 6 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.356+807G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26422207 | ||||||
chr2:26422233
|
A | T | 2 | a0008c0012t0001g0257a0008c0012t0001g0258 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.356+833A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26422233 | ||||||
chr2:26422246
|
A | G | 1 | a0002c0002t0001g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.356+846A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26422246 | ||||||
chr2:26422424
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02145.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.356+1024G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26422424 | ||||||
chr2:26422608
|
A | G | 1 | a0002c0002t0001g0158 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.356+1208A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26422608 | ||||||
chr2:26422728
|
C | T | 183 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.356+1328C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26422728 | ||||||
chr2:26422921
|
T | TA | 7 | a0001c0001t0001g0089a0002c0002t0001g0106a0003c0004t0001g0337others(4): Show | 7 | HG01934.hp2 HG02809.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.357-1332dupA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 26422921 | |||||
chr2:26422921
|
TA | T | 12 | a0001c0001t0001g0081a0002c0002t0001g0086a0002c0002t0001g0121others(9): Show | 12 | HG00408.hp1 HG01169.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.357-1332delA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 26422921 | |||||
chr2:26422961
|
T | G | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.357-1310T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26422961 | ||||||
chr2:26423047
|
C | T | 2 | a0001c0007t0001g0092a0001c0007t0001g0251 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.357-1224C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423047 | ||||||
chr2:26423163
|
G | A | 1 | a0004c0003t0001g0214 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.357-1108G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423163 | ||||||
chr2:26423163
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.357-1108G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423163 | ||||||
chr2:26423305
|
A | T | 24 | a0001c0007t0001g0092a0001c0007t0001g0251a0001c0007t0002g0293others(21): Show | 24 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.357-966A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423305 | ||||||
chr2:26423336
|
G | T | 1 | a0002c0002t0001g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.357-935G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423336 | ||||||
chr2:26423362
|
A | G | 1 | a0006c0008t0001g0188 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.357-909A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423362 | ||||||
chr2:26423458
|
G | A | 1 | a0002c0002t0001g0104 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.357-813G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423458 | ||||||
chr2:26423463
|
A | G | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.357-808A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423463 | ||||||
chr2:26423493
|
C | T | 1 | a0000c0021t0003g0327 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.357-778C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423493 | ||||||
chr2:26423594
|
C | T | 255 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.357-677C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423594 | ||||||
chr2:26423614
|
A | G | 3 | a0003c0004t0001g0029a0003c0004t0003g0025a0019c0027t0001g0344 | 3 | HG01109.hp2 HG01934.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.357-657A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423614 | ||||||
chr2:26423742
|
C | T | 1 | a0003c0004t0001g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.357-529C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423742 | ||||||
chr2:26423801
|
T | C | 19 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(16): Show | 19 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.357-470T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423801 | ||||||
chr2:26423814
|
C | T | 184 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.357-457C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26423814 | ||||||
chr2:26424011
|
C | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.357-260C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26424011 | ||||||
chr2:26424018
|
ATGTGTG | A | 25 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0268others(22): Show | 27 | HG00558.hp2 HG03041.hp2 NA18942.hp2 others(24): Show |
intron_variant | MODIFIER | c.357-243_357-238del others(6): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 26424018 | |||||
chr2:26424061
|
T | C | 1 | a0003c0004t0001g0262 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.357-210T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26424061 | ||||||
chr2:26424121
|
C | A | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.357-150C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26424121 | ||||||
chr2:26424146
|
G | A | 1 | a0022c0020t0001g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.357-125G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26424146 | ||||||
chr2:26424203
|
C | T | 17 | a0002c0002t0001g0103a0002c0002t0001g0104a0002c0002t0001g0161others(14): Show | 18 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.357-68C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 3/16 | chr2 | 26424203 | ||||||
chr2:26424466
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0089 | 2 | HG02300.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.540+12G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26424466 | ||||||
chr2:26424547
|
G | C | 7 | a0003c0004t0001g0328a0003c0004t0001g0329a0003c0004t0003g0264others(4): Show | 8 | HG00642.hp1 HG00738.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.540+93G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26424547 | ||||||
chr2:26424573
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0003g0220 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.540+119T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26424573 | ||||||
chr2:26424661
|
T | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.540+207T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26424661 | ||||||
chr2:26424670
|
G | C | 1 | a0002c0002t0001g0203 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.540+216G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26424670 | ||||||
chr2:26424960
|
CA | C | 5 | a0003c0005t0003g0261a0003c0005t0003g0358a0003c0005t0003g0359others(2): Show | 5 | HG01496.hp1 HG02572.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+511delA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26424960 | |||||
chr2:26425281
|
C | T | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+827C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26425281 | ||||||
chr2:26425659
|
C | T | 1 | a0002c0002t0001g0154 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.540+1205C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26425659 | ||||||
chr2:26425737
|
T | C | 7 | a0002c0002t0001g0010a0002c0002t0001g0130a0002c0002t0001g0131others(4): Show | 8 | HG00423.hp2 NA18964.hp2 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.540+1283T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26425737 | ||||||
chr2:26425793
|
T | C | 12 | a0001c0007t0001g0270a0001c0007t0001g0348a0001c0007t0001g0349others(9): Show | 12 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.540+1339T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26425793 | ||||||
chr2:26425851
|
C | T | 2 | a0001c0007t0001g0092a0001c0007t0001g0251 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.540+1397C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26425851 | ||||||
chr2:26425875
|
A | AT | 7 | a0001c0001t0001g0021a0001c0001t0001g0023a0002c0002t0001g0119others(4): Show | 7 | HG01978.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+1431dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26425875 | |||||
chr2:26425924
|
G | A | 1 | a0003c0004t0001g0314 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.540+1470G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26425924 | ||||||
chr2:26426153
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0053 | 3 | HG01106.hp2 HG01928.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.540+1699C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426153 | ||||||
chr2:26426217
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.540+1763T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426217 | ||||||
chr2:26426246
|
C | A | 1 | a0004c0003t0001g0252 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.540+1792C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426246 | ||||||
chr2:26426281
|
C | T | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+1827C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426281 | ||||||
chr2:26426370
|
A | AT | 44 | a0001c0001t0001g0077a0001c0007t0001g0092a0001c0007t0001g0251others(41): Show | 44 | HG00741.hp2 HG01109.hp2 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.540+1930dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26426370 | |||||
chr2:26426370
|
AT | A | 15 | a0001c0001t0001g0064a0008c0011t0001g0323a0008c0011t0001g0324others(12): Show | 16 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.540+1930delT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26426370 | |||||
chr2:26426389
|
C | T | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+1935C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426389 | ||||||
chr2:26426405
|
C | T | 1 | a0007c0009t0001g0186 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.540+1951C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426405 | ||||||
chr2:26426520
|
C | T | 1 | a0004c0003t0001g0249 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.540+2066C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426520 | ||||||
chr2:26426580
|
T | C | 1 | a0001c0001t0007g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.540+2126T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426580 | ||||||
chr2:26426586
|
C | T | 27 | a0001c0007t0001g0092a0001c0007t0001g0251a0001c0007t0002g0293others(24): Show | 27 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.540+2132C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426586 | ||||||
chr2:26426658
|
C | T | 1 | a0016c0030t0001g0361 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.540+2204C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426658 | ||||||
chr2:26426781
|
T | G | 1 | a0003c0004t0001g0263 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.540+2327T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426781 | ||||||
chr2:26426903
|
A | G | 6 | a0001c0007t0001g0270a0001c0007t0001g0348a0001c0007t0001g0349others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+2449A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426903 | ||||||
chr2:26426943
|
T | C | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+2489T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26426943 | ||||||
chr2:26427148
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0332a0003c0005t0003g0331 | 4 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-2480G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26427148 | ||||||
chr2:26427361
|
C | G | 1 | a0001c0016t0003g0279 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.541-2267C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26427361 | ||||||
chr2:26427425
|
A | T | 27 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0268others(24): Show | 29 | HG00558.hp2 HG02280.hp1 HG03041.hp2 others(26): Show |
intron_variant | MODIFIER | c.541-2203A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26427425 | ||||||
chr2:26427551
|
T | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.541-2077T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26427551 | ||||||
chr2:26427568
|
T | C | 3 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0025t0001g0356 | 3 | HG02809.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.541-2060T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26427568 | ||||||
chr2:26427585
|
A | ATACTCTT others(4): Show |
1 | a0001c0001t0002g0305 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.541-2041_541-2031d others(13): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26427585 | |||||
chr2:26427768
|
T | C | 1 | a0002c0002t0001g0100 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.541-1860T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26427768 | ||||||
chr2:26427791
|
A | C | 2 | a0003c0004t0001g0029a0003c0004t0003g0025 | 2 | HG01934.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.541-1837A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26427791 | ||||||
chr2:26427862
|
G | A | 15 | a0005c0006t0001g0226a0008c0011t0001g0323a0008c0011t0001g0324others(12): Show | 16 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.541-1766G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26427862 | ||||||
chr2:26427869
|
C | A | 2 | a0003c0004t0002g0283a0003c0004t0002g0284 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.541-1759C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26427869 | ||||||
chr2:26428023
|
T | C | 12 | a0001c0007t0001g0270a0001c0007t0001g0348a0001c0007t0001g0349others(9): Show | 12 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.541-1605T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428023 | ||||||
chr2:26428260
|
A | G | 16 | a0003c0004t0001g0029a0003c0004t0003g0025a0008c0011t0001g0323others(13): Show | 17 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.541-1368A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428260 | ||||||
chr2:26428388
|
A | G | 2 | a0003c0004t0003g0264a0003c0004t0003g0265 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.541-1240A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428388 | ||||||
chr2:26428427
|
C | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0332a0003c0005t0003g0331 | 4 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-1201C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428427 | ||||||
chr2:26428494
|
G | C | 1 | a0003c0004t0001g0328 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.541-1134G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428494 | ||||||
chr2:26428527
|
G | A | 25 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0268others(22): Show | 27 | HG00558.hp2 HG03041.hp2 NA18942.hp2 others(24): Show |
intron_variant | MODIFIER | c.541-1101G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428527 | ||||||
chr2:26428564
|
C | T | 4 | a0001c0001t0004g0212a0003c0004t0003g0312a0003c0004t0003g0313others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-1064C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428564 | ||||||
chr2:26428708
|
A | G | 256 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.541-920A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428708 | ||||||
chr2:26428739
|
A | C | 209 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.541-889A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428739 | ||||||
chr2:26428792
|
T | C | 263 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(260): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.541-836T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428792 | ||||||
chr2:26428797
|
C | CA | 27 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0268others(24): Show | 29 | HG00558.hp2 HG02280.hp1 HG03041.hp2 others(26): Show |
intron_variant | MODIFIER | c.541-819dupA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26428797 | |||||
chr2:26428852
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.541-776C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428852 | ||||||
chr2:26428854
|
A | G | 1 | a0005c0006t0001g0247 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.541-774A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26428854 | ||||||
chr2:26429065
|
G | A | 3 | a0004c0003t0001g0228a0004c0003t0001g0229a0004c0003t0001g0234 | 3 | NA19054.hp2 NA19058.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.541-563G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429065 | ||||||
chr2:26429181
|
AGAT | A | 14 | a0001c0001t0001g0021a0001c0001t0002g0015a0001c0001t0002g0303others(11): Show | 15 | HG00609.hp2 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.541-443_541-441del others(3): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429181 | |||||
chr2:26429182
|
G | GATT | 3 | a0001c0007t0001g0348a0001c0007t0001g0349a0001c0007t0001g0353 | 3 | HG02622.hp1 HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.541-444_541-443ins others(3): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429182 | |||||
chr2:26429182
|
GATGATT | G | 32 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0332others(29): Show | 34 | HG00408.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.541-443_541-438del others(6): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429182 | |||||
chr2:26429182
|
GATGATTA others(2): Show |
G | 44 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(41): Show | 44 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.541-443_541-435del others(9): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429182 | |||||
chr2:26429182
|
GATGATTA others(5): Show |
G | 4 | a0001c0001t0003g0038a0001c0001t0003g0074a0003c0004t0001g0320others(1): Show | 4 | HG02280.hp1 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-443_541-432del others(12): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429182 | |||||
chr2:26429182
|
GATGATTA others(8): Show |
G | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.541-443_541-429del others(15): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429182 | |||||
chr2:26429182
|
GATGATTA others(11): Show |
G | 5 | a0001c0001t0001g0059a0003c0004t0001g0029a0003c0004t0003g0025others(2): Show | 5 | HG01109.hp1 HG01934.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-443_541-426del others(18): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429182 | |||||
chr2:26429182
|
GATGATTA others(14): Show |
G | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.541-443_541-423del others(21): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429182 | |||||
chr2:26429185
|
G | GATT | 3 | a0001c0007t0003g0266a0002c0002t0001g0132a0003c0004t0001g0107 | 3 | HG00609.hp1 HG02886.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.541-397_541-395dup others(3): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429185 | |||||
chr2:26429185
|
G | T | 9 | a0000c0021t0003g0327a0001c0007t0001g0270a0001c0007t0001g0348others(6): Show | 9 | HG02135.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.541-443G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429185 | ||||||
chr2:26429185
|
GATT | G | 52 | a0001c0007t0001g0144a0001c0007t0003g0269a0001c0016t0003g0278others(49): Show | 58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.541-397_541-395del others(3): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429185 | |||||
chr2:26429185
|
GATTATT | G | 34 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0010others(31): Show | 37 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.541-400_541-395del others(6): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429185 | |||||
chr2:26429185
|
GATTATTA others(2): Show |
G | 5 | a0002c0002t0001g0101a0002c0002t0001g0117a0002c0002t0001g0126others(2): Show | 5 | HG00673.hp2 NA18984.hp2 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-403_541-395del others(9): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429185 | |||||
chr2:26429185
|
GATTATTA others(5): Show |
G | 1 | a0002c0002t0001g0164 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.541-406_541-395del others(12): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429185 | |||||
chr2:26429185
|
GATTATTA others(11): Show |
G | 2 | a0002c0002t0001g0118a0002c0002t0001g0121 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.541-412_541-395del others(18): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 26429185 | |||||
chr2:26429188
|
T | G | 1 | a0009c0010t0001g0281 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.541-440T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429188 | ||||||
chr2:26429191
|
T | G | 5 | a0003c0004t0001g0328a0003c0004t0001g0329a0009c0010t0001g0013others(2): Show | 6 | HG00642.hp1 HG00738.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-437T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429191 | ||||||
chr2:26429194
|
T | G | 5 | a0003c0004t0001g0328a0003c0004t0001g0329a0009c0010t0001g0013others(2): Show | 6 | HG00642.hp1 HG00738.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-434T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429194 | ||||||
chr2:26429197
|
T | G | 5 | a0003c0004t0003g0264a0003c0004t0003g0265a0009c0010t0001g0013others(2): Show | 6 | HG00738.hp1 HG02145.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-431T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429197 | ||||||
chr2:26429200
|
T | G | 4 | a0003c0004t0003g0264a0003c0004t0003g0265a0009c0010t0001g0013others(1): Show | 5 | HG00738.hp1 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-428T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429200 | ||||||
chr2:26429298
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.541-330C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429298 | ||||||
chr2:26429317
|
G | A | 1 | a0004c0003t0001g0200 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.541-311G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429317 | ||||||
chr2:26429318
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.541-310C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429318 | ||||||
chr2:26429361
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.541-267G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429361 | ||||||
chr2:26429407
|
G | C | 1 | a0002c0002t0001g0148 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.541-221G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429407 | ||||||
chr2:26429425
|
C | T | 2 | a0004c0003t0001g0232a0004c0003t0001g0233 | 2 | HG02132.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.541-203C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429425 | ||||||
chr2:26429532
|
A | G | 19 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(16): Show | 19 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.541-96A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 4/16 | chr2 | 26429532 | ||||||
chr2:26429803
|
A | G | 256 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.678+38A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26429803 | ||||||
chr2:26429807
|
C | G | 1 | a0001c0001t0002g0305 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.678+42C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26429807 | ||||||
chr2:26429811
|
T | C | 1 | a0001c0001t0002g0305 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.678+46T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26429811 | ||||||
chr2:26429812
|
G | T | 1 | a0001c0001t0002g0305 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.678+47G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26429812 | ||||||
chr2:26429871
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.678+106C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26429871 | ||||||
chr2:26429925
|
A | G | 1 | a0019c0027t0001g0344 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.678+160A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26429925 | ||||||
chr2:26430030
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.678+265A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430030 | ||||||
chr2:26430125
|
G | A | 1 | a0003c0005t0003g0362 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.678+360G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430125 | ||||||
chr2:26430142
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.678+377G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430142 | ||||||
chr2:26430441
|
C | T | 19 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(16): Show | 19 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.679-345C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430441 | ||||||
chr2:26430477
|
G | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0332 | 3 | HG01069.hp2 HG01071.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.679-309G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430477 | ||||||
chr2:26430484
|
C | T | 2 | a0004c0003t0001g0045a0004c0003t0001g0049 | 2 | HG03831.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.679-302C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430484 | ||||||
chr2:26430509
|
G | A | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.679-277G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430509 | ||||||
chr2:26430519
|
A | G | 2 | a0011c0015t0001g0016a0011c0015t0001g0357 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.679-267A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430519 | ||||||
chr2:26430589
|
G | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.679-197G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430589 | ||||||
chr2:26430637
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.679-149C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430637 | ||||||
chr2:26430680
|
A | G | 3 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0025t0001g0356 | 3 | HG02809.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.679-106A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 5/16 | chr2 | 26430680 | ||||||
chr2:26430947
|
C | T | 1 | a0003c0004t0002g0296 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.765+75C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26430947 | ||||||
chr2:26430958
|
C | CT | 187 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.765+106dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 26430958 | |||||
chr2:26430958
|
C | CTT | 33 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0330others(30): Show | 33 | HG00408.hp1 HG00609.hp2 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.765+105_765+106dup others(2): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 26430958 | |||||
chr2:26430958
|
CT | C | 8 | a0002c0002t0001g0084a0002c0002t0001g0094a0002c0002t0001g0122others(5): Show | 8 | HG01934.hp1 HG02559.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.765+106delT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 26430958 | |||||
chr2:26430958
|
CTTTTTTT others(4): Show |
C | 1 | a0019c0027t0001g0344 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.765+96_765+106delT others(10): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 26430958 | |||||
chr2:26431016
|
T | C | 1 | a0019c0027t0001g0344 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.765+144T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26431016 | ||||||
chr2:26431065
|
A | G | 8 | a0002c0002t0001g0096a0002c0002t0001g0146a0002c0002t0001g0151others(5): Show | 8 | HG00558.hp1 HG00621.hp2 NA18993.hp2 others(5): Show |
intron_variant | MODIFIER | c.765+193A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26431065 | ||||||
chr2:26431115
|
C | T | 5 | a0003c0005t0003g0261a0003c0005t0003g0358a0003c0005t0003g0359others(2): Show | 5 | HG01496.hp1 HG02572.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.765+243C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26431115 | ||||||
chr2:26431144
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.765+272C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26431144 | ||||||
chr2:26431145
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0332a0003c0005t0003g0331 | 4 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+273G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26431145 | ||||||
chr2:26431176
|
G | C | 2 | a0003c0004t0001g0029a0003c0004t0003g0025 | 2 | HG01934.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.765+304G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26431176 | ||||||
chr2:26431190
|
A | G | 256 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.765+318A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26431190 | ||||||
chr2:26431376
|
C | G | 13 | a0001c0001t0001g0347a0001c0007t0001g0270a0001c0007t0001g0348others(10): Show | 13 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.765+504C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26431376 | ||||||
chr2:26431611
|
C | CT | 7 | a0003c0005t0003g0261a0003c0005t0003g0358a0003c0005t0003g0359others(4): Show | 8 | HG01243.hp2 HG01496.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.766-263dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 26431611 | |||||
chr2:26431698
|
G | A | 1 | a0001c0007t0001g0270 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.766-186G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26431698 | ||||||
chr2:26431823
|
G | A | 3 | a0003c0004t0003g0312a0003c0004t0003g0313a0003c0004t0003g0321 | 3 | HG02622.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766-61G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 6/16 | chr2 | 26431823 | ||||||
chr2:26432098
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.888+92T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26432098 | ||||||
chr2:26432287
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0003g0352 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.888+281C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26432287 | ||||||
chr2:26432438
|
A | G | 256 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.888+432A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26432438 | ||||||
chr2:26432439
|
T | A | 1 | a0003c0004t0001g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.888+433T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26432439 | ||||||
chr2:26432440
|
A | G | 1 | a0003c0004t0001g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.888+434A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26432440 | ||||||
chr2:26432461
|
T | G | 2 | a0001c0001t0001g0335a0001c0001t0001g0345 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.888+455T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26432461 | ||||||
chr2:26432493
|
TGTGAGAA others(1): Show |
T | 12 | a0001c0007t0001g0270a0001c0007t0001g0348a0001c0007t0001g0349others(9): Show | 12 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.888+489_888+496del others(8): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26432493 | |||||
chr2:26432605
|
A | AAAAG | 254 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.888+604_888+607dup others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26432605 | |||||
chr2:26432721
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.888+715C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26432721 | ||||||
chr2:26432877
|
C | T | 201 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.888+871C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26432877 | ||||||
chr2:26433042
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0065others(1): Show | 4 | HG01069.hp1 HG01123.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.888+1036G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433042 | ||||||
chr2:26433084
|
G | T | 31 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(28): Show | 33 | HG00558.hp2 HG02109.hp1 HG02280.hp2 others(30): Show |
intron_variant | MODIFIER | c.888+1078G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433084 | ||||||
chr2:26433114
|
A | T | 12 | a0001c0007t0001g0270a0001c0007t0001g0348a0001c0007t0001g0349others(9): Show | 12 | HG00741.hp2 HG02055.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.888+1108A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433114 | ||||||
chr2:26433168
|
A | C | 1 | a0002c0002t0001g0131 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.888+1162A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433168 | ||||||
chr2:26433226
|
G | A | 1 | a0001c0001t0004g0212 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.888+1220G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433226 | ||||||
chr2:26433274
|
C | T | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.888+1268C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433274 | ||||||
chr2:26433386
|
T | C | 1 | a0004c0003t0001g0201 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.888+1380T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433386 | ||||||
chr2:26433495
|
T | C | 1 | a0002c0002t0001g0162 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.888+1489T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433495 | ||||||
chr2:26433584
|
T | C | 1 | a0002c0002t0001g0139 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.888+1578T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433584 | ||||||
chr2:26433850
|
A | T | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.888+1844A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433850 | ||||||
chr2:26433862
|
C | A | 16 | a0003c0004t0001g0029a0003c0004t0003g0025a0008c0011t0001g0323others(13): Show | 17 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.888+1856C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433862 | ||||||
chr2:26433891
|
G | A | 1 | a0019c0027t0001g0344 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.888+1885G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433891 | ||||||
chr2:26433970
|
A | T | 1 | a0003c0005t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.888+1964A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26433970 | ||||||
chr2:26434003
|
T | C | 5 | a0003c0004t0001g0259a0003c0004t0001g0260a0003c0004t0001g0263others(2): Show | 5 | HG02809.hp1 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.888+1997T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26434003 | ||||||
chr2:26434111
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0059a0001c0007t0001g0270others(30): Show | 34 | HG00408.hp1 HG00609.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.888+2105T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26434111 | ||||||
chr2:26434141
|
G | A | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.888+2135G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26434141 | ||||||
chr2:26434179
|
A | C | 14 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(11): Show | 15 | HG00733.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.888+2173A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26434179 | ||||||
chr2:26434395
|
G | A | 1 | a0003c0004t0001g0314 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.888+2389G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26434395 | ||||||
chr2:26434582
|
C | T | 1 | a0006c0008t0001g0184 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.888+2576C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26434582 | ||||||
chr2:26434823
|
G | A | 1 | a0002c0002t0001g0151 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.888+2817G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26434823 | ||||||
chr2:26434890
|
C | CA | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.888+2899dupA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26434890 | |||||
chr2:26434890
|
C | CAA | 7 | a0001c0007t0001g0092a0001c0007t0001g0251a0004c0003t0001g0216others(4): Show | 7 | HG01192.hp1 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.888+2898_888+2899d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26434890 | |||||
chr2:26435224
|
G | T | 1 | a0004c0003t0001g0088 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.888+3218G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26435224 | ||||||
chr2:26435328
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.888+3322A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26435328 | ||||||
chr2:26435344
|
T | C | 2 | a0003c0004t0001g0029a0003c0004t0003g0025 | 2 | HG01934.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.888+3338T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26435344 | ||||||
chr2:26435368
|
C | T | 1 | a0001c0001t0003g0352 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.888+3362C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26435368 | ||||||
chr2:26435625
|
A | C | 209 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.888+3619A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26435625 | ||||||
chr2:26435751
|
C | CT | 10 | a0003c0004t0001g0029a0003c0004t0003g0025a0008c0011t0001g0323others(7): Show | 10 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.888+3758dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26435751 | |||||
chr2:26435841
|
T | C | 1 | a0002c0002t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.888+3835T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26435841 | ||||||
chr2:26435924
|
T | A | 6 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.888+3918T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26435924 | ||||||
chr2:26436127
|
C | CT | 11 | a0003c0004t0001g0029a0003c0004t0003g0025a0007c0009t0001g0174others(8): Show | 11 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.888+4133dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26436127 | |||||
chr2:26436377
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.889-4001C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26436377 | ||||||
chr2:26436436
|
C | T | 2 | a0011c0015t0001g0016a0011c0015t0001g0357 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.889-3942C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26436436 | ||||||
chr2:26436440
|
T | G | 1 | a0001c0001t0001g0308 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.889-3938T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26436440 | ||||||
chr2:26436481
|
T | A | 1 | a0001c0007t0001g0350 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.889-3897T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26436481 | ||||||
chr2:26436484
|
AT | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(5): Show | 8 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.889-3885delT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26436484 | |||||
chr2:26436494
|
G | A | 1 | a0020c0026t0001g0114 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.889-3884G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26436494 | ||||||
chr2:26436668
|
G | A | 1 | a0002c0002t0001g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.889-3710G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26436668 | ||||||
chr2:26436711
|
GTTGTA | G | 6 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0004t0001g0360others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-3661_889-3657d others(7): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26436711 | |||||
chr2:26436729
|
A | G | 8 | a0002c0002t0001g0009a0002c0002t0001g0129a0002c0002t0001g0132others(5): Show | 9 | HG00408.hp2 HG00544.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-3649A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26436729 | ||||||
chr2:26436871
|
G | A | 97 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0007others(94): Show | 105 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.889-3507G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26436871 | ||||||
chr2:26437024
|
T | C | 2 | a0002c0002t0001g0100a0002c0002t0001g0146 | 2 | NA19012.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.889-3354T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437024 | ||||||
chr2:26437056
|
G | A | 1 | a0006c0008t0001g0184 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.889-3322G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437056 | ||||||
chr2:26437182
|
C | A | 1 | a0007c0009t0001g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.889-3196C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437182 | ||||||
chr2:26437214
|
G | C | 1 | a0016c0030t0001g0361 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.889-3164G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437214 | ||||||
chr2:26437276
|
C | A | 1 | a0002c0002t0001g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.889-3102C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437276 | ||||||
chr2:26437303
|
G | A | 1 | a0002c0002t0001g0166 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.889-3075G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437303 | ||||||
chr2:26437387
|
G | A | 66 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0334others(63): Show | 68 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.889-2991G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437387 | ||||||
chr2:26437439
|
C | T | 2 | a0001c0007t0003g0269a0003c0004t0001g0328 | 2 | HG00642.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.889-2939C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437439 | ||||||
chr2:26437723
|
C | T | 5 | a0003c0005t0003g0261a0003c0005t0003g0358a0003c0005t0003g0359others(2): Show | 5 | HG01496.hp1 HG02572.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-2655C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437723 | ||||||
chr2:26437803
|
G | A | 66 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0334others(63): Show | 68 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.889-2575G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437803 | ||||||
chr2:26437878
|
C | T | 34 | a0001c0007t0001g0092a0001c0007t0001g0251a0001c0007t0002g0293others(31): Show | 34 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.889-2500C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26437878 | ||||||
chr2:26438049
|
G | A | 1 | a0002c0002t0001g0127 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.889-2329G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26438049 | ||||||
chr2:26438070
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 55 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.889-2308C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26438070 | ||||||
chr2:26438074
|
A | C | 6 | a0008c0012t0001g0257a0008c0012t0001g0258a0008c0012t0001g0343others(3): Show | 7 | HG01243.hp2 HG02559.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-2304A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26438074 | ||||||
chr2:26438087
|
C | CA | 19 | a0001c0001t0001g0055a0001c0001t0001g0066a0001c0001t0001g0077others(16): Show | 19 | HG00642.hp2 HG01433.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.889-2267dupA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26438087 | |||||
chr2:26438087
|
C | CAA | 7 | a0001c0001t0001g0031a0002c0002t0001g0115a0002c0002t0001g0134others(4): Show | 8 | HG01123.hp1 HG01243.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.889-2268_889-2267d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26438087 | |||||
chr2:26438087
|
CA | C | 25 | a0001c0001t0001g0053a0001c0001t0001g0336a0001c0007t0001g0092others(22): Show | 25 | HG01109.hp2 HG02451.hp1 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.889-2267delA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26438087 | |||||
chr2:26438087
|
CAA | C | 9 | a0000c0021t0003g0327a0001c0001t0001g0017a0001c0001t0001g0047others(6): Show | 10 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.889-2268_889-2267d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26438087 | |||||
chr2:26438087
|
CAAA | C | 26 | a0001c0007t0002g0293a0001c0007t0002g0295a0003c0004t0001g0024others(23): Show | 26 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.889-2269_889-2267d others(5): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26438087 | |||||
chr2:26438201
|
T | C | 28 | a0001c0007t0001g0092a0001c0007t0001g0251a0001c0007t0002g0293others(25): Show | 28 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.889-2177T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26438201 | ||||||
chr2:26438236
|
A | T | 1 | a0002c0002t0001g0159 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.889-2142A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26438236 | ||||||
chr2:26438406
|
A | G | 3 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333 | 3 | HG01891.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.889-1972A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26438406 | ||||||
chr2:26438598
|
C | T | 6 | a0008c0012t0001g0257a0008c0012t0001g0258a0008c0012t0001g0343others(3): Show | 7 | HG01243.hp2 HG02559.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-1780C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26438598 | ||||||
chr2:26438606
|
C | G | 4 | a0008c0012t0001g0257a0008c0012t0001g0258a0008c0012t0001g0343others(1): Show | 4 | HG02886.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1772C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26438606 | ||||||
chr2:26438963
|
A | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0059a0006c0008t0001g0175others(24): Show | 29 | HG00408.hp1 HG00609.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.889-1415A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26438963 | ||||||
chr2:26439198
|
C | G | 3 | a0002c0002t0001g0010a0002c0002t0001g0138a0002c0002t0001g0140 | 4 | NA18964.hp2 NA18997.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-1180C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439198 | ||||||
chr2:26439207
|
G | A | 4 | a0000c0021t0003g0327a0001c0001t0001g0017a0001c0001t0001g0332others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-1171G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439207 | ||||||
chr2:26439213
|
C | T | 28 | a0001c0007t0001g0092a0001c0007t0001g0251a0001c0007t0002g0293others(25): Show | 28 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.889-1165C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439213 | ||||||
chr2:26439231
|
G | A | 21 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(18): Show | 22 | HG00408.hp1 HG00609.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.889-1147G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439231 | ||||||
chr2:26439270
|
C | A | 1 | a0002c0002t0006g0097 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.889-1108C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439270 | ||||||
chr2:26439532
|
G | A | 1 | a0010c0013t0001g0199 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.889-846G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439532 | ||||||
chr2:26439565
|
C | T | 4 | a0000c0021t0003g0327a0001c0001t0001g0017a0001c0001t0001g0332others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-813C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439565 | ||||||
chr2:26439708
|
T | G | 255 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.889-670T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439708 | ||||||
chr2:26439869
|
C | T | 1 | a0001c0001t0002g0297 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.889-509C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439869 | ||||||
chr2:26439922
|
A | AAAATATA others(25): Show |
1 | a0006c0008t0001g0176 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.889-455_889-454ins others(32): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AAAATATA others(27): Show |
1 | a0006c0008t0001g0177 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.889-455_889-454ins others(34): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AAAATATA others(29): Show |
1 | a0006c0008t0001g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.889-455_889-454ins others(36): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AAAATATA others(31): Show |
1 | a0006c0008t0001g0175 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.889-455_889-454ins others(38): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AAAATATA others(35): Show |
1 | a0006c0008t0001g0184 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.889-455_889-454ins others(42): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATAT | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0047others(2): Show | 5 | HG01074.hp2 HG01884.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-446_889-441dup others(6): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(3): Show |
2 | a0007c0009t0001g0182a0007c0009t0001g0183 | 2 | NA18612.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.889-450_889-441dup others(10): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(5): Show |
2 | a0008c0012t0001g0343a0008c0012t0008g0346 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.889-452_889-441dup others(12): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0315a0008c0012t0001g0257 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.889-454_889-441dup others(14): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(9): Show |
1 | a0008c0012t0001g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.889-441_889-440ins others(16): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(11): Show |
1 | a0004c0003t0001g0322 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.889-441_889-440ins others(18): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(15): Show |
2 | a0001c0001t0001g0079a0001c0001t0004g0192 | 2 | HG03098.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.889-441_889-440ins others(22): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(17): Show |
1 | a0004c0003t0001g0194 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.889-441_889-440ins others(24): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(19): Show |
6 | a0001c0001t0001g0204a0001c0001t0001g0208a0001c0001t0003g0209others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(26): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(21): Show |
13 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0091others(10): Show | 13 | HG00741.hp2 HG01081.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(28): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(23): Show |
17 | a0000c0021t0003g0327a0001c0001t0001g0043a0001c0001t0001g0089others(14): Show | 17 | HG00639.hp1 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(30): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(25): Show |
11 | a0001c0001t0001g0027a0001c0001t0001g0224a0001c0001t0001g0253others(8): Show | 11 | HG00280.hp1 HG01123.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(32): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(27): Show |
26 | a0001c0001t0001g0026a0001c0001t0001g0044a0001c0001t0001g0048others(23): Show | 26 | HG00438.hp2 HG00639.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(34): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(29): Show |
8 | a0001c0001t0004g0250a0003c0005t0001g0299a0004c0003t0001g0200others(5): Show | 8 | HG00099.hp1 HG02004.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(36): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(31): Show |
6 | a0001c0001t0004g0090a0001c0001t0007g0050a0004c0003t0001g0058others(3): Show | 6 | HG04184.hp1 NA18945.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(38): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(33): Show |
3 | a0003c0005t0001g0298a0004c0003t0001g0255a0010c0013t0001g0199 | 3 | HG00642.hp2 NA18979.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(40): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(35): Show |
4 | a0003c0005t0001g0307a0004c0003t0001g0228a0004c0003t0001g0233others(1): Show | 4 | HG00558.hp2 HG02132.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(42): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(37): Show |
3 | a0001c0001t0001g0017a0003c0005t0001g0274a0004c0003t0001g0229 | 4 | HG01069.hp2 HG01071.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(44): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(39): Show |
3 | a0003c0005t0001g0022a0004c0003t0001g0231a0005c0006t0001g0235 | 3 | HG03209.hp2 NA18612.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(46): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
A | AATATATA others(41): Show |
1 | a0001c0001t0001g0332 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.889-441_889-440ins others(48): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439922
|
AAT | A | 2 | a0011c0015t0001g0016a0011c0015t0001g0357 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.889-442_889-441del others(2): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439922 | |||||
chr2:26439934
|
T | TATATATA others(19): Show |
2 | a0001c0001t0001g0335a0001c0001t0001g0345 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(26): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439934 | |||||
chr2:26439934
|
T | TATATATA others(21): Show |
1 | a0001c0001t0001g0338 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.889-441_889-440ins others(28): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439934 | |||||
chr2:26439934
|
T | TATATATA others(25): Show |
1 | a0001c0001t0001g0341 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.889-441_889-440ins others(32): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439934 | |||||
chr2:26439934
|
T | TATATATA others(29): Show |
1 | a0001c0001t0001g0340 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.889-441_889-440ins others(36): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439934 | |||||
chr2:26439934
|
T | TATATATA others(31): Show |
2 | a0001c0001t0001g0336a0001c0001t0001g0339 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(38): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439934 | |||||
chr2:26439934
|
T | TATATATA others(33): Show |
1 | a0001c0001t0001g0334 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.889-441_889-440ins others(40): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439934 | |||||
chr2:26439936
|
T | TATATATA others(5): Show |
1 | a0001c0007t0002g0293 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.889-441_889-440ins others(12): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(11): Show |
1 | a0001c0007t0003g0351 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.889-441_889-440ins others(18): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(22): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(19): Show |
2 | a0001c0007t0001g0092a0001c0007t0001g0251 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(26): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(17): Show |
1 | a0004c0003t0001g0193 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.889-441_889-440ins others(24): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(19): Show |
10 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0268others(7): Show | 12 | NA18952.hp2 NA18963.hp2 NA18968.hp2 others(9): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(26): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(25): Show |
1 | a0003c0004t0002g0296 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.889-441_889-440ins others(32): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(21): Show |
9 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0002g0285others(6): Show | 9 | HG03239.hp2 HG03654.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(28): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(25): Show |
2 | a0003c0004t0001g0024a0021c0024t0002g0294 | 2 | NA18906.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(32): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(23): Show |
2 | a0001c0001t0001g0055a0001c0001t0002g0290 | 2 | HG03831.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(30): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(25): Show |
2 | a0003c0004t0001g0263a0003c0005t0003g0362 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(32): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(27): Show |
10 | a0001c0007t0002g0295a0003c0004t0001g0172a0003c0004t0001g0316others(7): Show | 10 | HG02027.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(34): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(25): Show |
26 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0030others(23): Show | 27 | HG00280.hp2 HG00408.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(32): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(27): Show |
5 | a0001c0001t0001g0062a0003c0004t0001g0259a0003c0004t0001g0262others(2): Show | 5 | HG02004.hp2 HG02559.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(34): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(29): Show |
2 | a0001c0001t0001g0003a0019c0027t0001g0344 | 3 | HG00741.hp1 HG01074.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(36): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(27): Show |
16 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0035others(13): Show | 17 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(34): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(29): Show |
3 | a0003c0005t0001g0020a0003c0005t0003g0358a0003c0005t0003g0359 | 3 | HG01496.hp1 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.889-441_889-440ins others(36): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(31): Show |
2 | a0003c0004t0001g0314a0003c0004t0001g0319 | 2 | HG01346.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.889-441_889-440ins others(38): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(29): Show |
9 | a0001c0001t0001g0036a0001c0001t0001g0211a0001c0001t0003g0074others(6): Show | 9 | HG00099.hp2 HG00544.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(36): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(31): Show |
2 | a0003c0004t0001g0029a0003c0005t0001g0019 | 2 | HG01934.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(38): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(31): Show |
5 | a0001c0001t0001g0056a0001c0001t0001g0069a0001c0001t0001g0071others(2): Show | 5 | HG01258.hp1 NA18941.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(38): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(33): Show |
4 | a0001c0001t0001g0031a0001c0001t0001g0057a0001c0001t0001g0066others(1): Show | 4 | HG01123.hp1 HG01975.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-441_889-440ins others(40): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(35): Show |
2 | a0003c0004t0001g0260a0003c0005t0003g0261 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.889-441_889-440ins others(42): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(35): Show |
1 | a0007c0009t0001g0186 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.889-441_889-440ins others(42): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439936
|
T | TATATATA others(41): Show |
2 | a0003c0004t0002g0283a0003c0004t0002g0284 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.889-441_889-440ins others(48): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439936 | |||||
chr2:26439938
|
C | T | 16 | a0001c0001t0004g0090a0003c0004t0001g0328a0003c0004t0001g0329others(13): Show | 17 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.889-440C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439938 | ||||||
chr2:26439948
|
T | C | 15 | a0003c0004t0001g0029a0003c0004t0001g0259a0003c0004t0001g0260others(12): Show | 15 | HG01934.hp1 HG02071.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.889-430T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439948 | ||||||
chr2:26439948
|
TAC | T | 3 | a0002c0002t0001g0117a0002c0002t0001g0168a0017c0022t0001g0173 | 3 | HG00438.hp1 HG00673.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.889-416_889-415del others(2): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439948 | |||||
chr2:26439950
|
C | T | 15 | a0003c0004t0001g0029a0003c0004t0001g0259a0003c0004t0001g0260others(12): Show | 15 | HG01934.hp1 HG02071.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.889-428C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439950 | ||||||
chr2:26439962
|
CAT | C | 18 | a0006c0008t0001g0179a0006c0008t0001g0180a0006c0008t0001g0181others(15): Show | 19 | HG00408.hp1 HG00609.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.889-406_889-405del others(2): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26439962 | |||||
chr2:26439964
|
T | C | 7 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(4): Show | 7 | HG02071.hp1 HG02080.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-414T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439964 | ||||||
chr2:26439972
|
T | C | 5 | a0003c0004t0001g0259a0003c0004t0001g0260a0003c0004t0001g0263others(2): Show | 5 | HG02809.hp1 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.889-406T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26439972 | ||||||
chr2:26440094
|
T | G | 1 | a0002c0002t0001g0102 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.889-284T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26440094 | ||||||
chr2:26440277
|
A | G | 3 | a0009c0010t0001g0013a0009c0010t0001g0267a0009c0010t0001g0281 | 4 | HG00738.hp1 HG02145.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-101A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26440277 | ||||||
chr2:26440319
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.889-59T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26440319 | ||||||
chr2:26440319
|
T | TTG | 115 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0027others(112): Show | 116 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.889-33_889-32dupGT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26440319 | |||||
chr2:26440319
|
T | TTGTG | 40 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(37): Show | 44 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.889-35_889-32dupGT others(2): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26440319 | |||||
chr2:26440319
|
TTG | T | 68 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0268others(65): Show | 70 | HG00558.hp2 HG00733.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.889-33_889-32delGT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26440319 | |||||
chr2:26440343
|
G | A | 1 | a0016c0030t0001g0361 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.889-35G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26440343 | ||||||
chr2:26440345
|
G | A | 48 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0268others(45): Show | 51 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.889-33G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26440345 | ||||||
chr2:26440345
|
G | GTA | 10 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0007t0001g0270others(7): Show | 10 | HG02165.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.889-18_889-17dupTA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 26440345 | |||||
chr2:26440347
|
A | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(53): Show | 57 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.889-31A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 7/16 | chr2 | 26440347 | ||||||
chr2:26440601
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1028+84G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26440601 | ||||||
chr2:26440676
|
C | T | 1 | a0003c0004t0001g0107 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1028+159C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26440676 | ||||||
chr2:26440722
|
G | T | 6 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1028+205G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26440722 | ||||||
chr2:26440747
|
A | G | 2 | a0001c0007t0001g0092a0001c0007t0001g0251 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1028+230A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26440747 | ||||||
chr2:26440848
|
A | C | 6 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1028+331A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26440848 | ||||||
chr2:26440955
|
C | T | 1 | a0003c0004t0001g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1028+438C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26440955 | ||||||
chr2:26441459
|
C | T | 144 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1028+942C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26441459 | ||||||
chr2:26441544
|
A | G | 19 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(16): Show | 19 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.1028+1027A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26441544 | ||||||
chr2:26441719
|
AAGGTAGG | A | 22 | a0004c0029t0001g0109a0006c0008t0001g0175a0006c0008t0001g0176others(19): Show | 23 | HG00408.hp1 HG00609.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1028+1206_1028+121 others(11): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 26441719 | |||||
chr2:26441818
|
G | C | 1 | a0003c0004t0001g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1028+1301G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26441818 | ||||||
chr2:26441843
|
TC | T | 6 | a0003c0004t0001g0337a0003c0004t0001g0342a0003c0004t0001g0360others(3): Show | 6 | HG00741.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1028+1327delC | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26441843 | ||||||
chr2:26441953
|
G | T | 1 | a0002c0002t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1028+1436G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26441953 | ||||||
chr2:26441954
|
T | G | 1 | a0002c0002t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1028+1437T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26441954 | ||||||
chr2:26442259
|
C | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0303 | 3 | NA18952.hp2 NA18986.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1028+1742C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442259 | ||||||
chr2:26442283
|
C | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1028+1766C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442283 | ||||||
chr2:26442292
|
C | T | 1 | a0010c0013t0001g0199 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1028+1775C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442292 | ||||||
chr2:26442488
|
G | T | 1 | a0003c0005t0003g0331 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1029-1734G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442488 | ||||||
chr2:26442525
|
A | G | 1 | a0002c0002t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1029-1697A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442525 | ||||||
chr2:26442526
|
G | A | 1 | a0002c0002t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1029-1696G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442526 | ||||||
chr2:26442534
|
A | G | 1 | a0018c0023t0001g0198 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1029-1688A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442534 | ||||||
chr2:26442621
|
T | C | 1 | a0004c0003t0001g0194 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1029-1601T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442621 | ||||||
chr2:26442847
|
G | A | 1 | a0002c0002t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1029-1375G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442847 | ||||||
chr2:26442848
|
C | G | 1 | a0002c0002t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1029-1374C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442848 | ||||||
chr2:26442928
|
G | A | 25 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0268others(22): Show | 27 | HG00558.hp2 HG03041.hp2 NA18942.hp2 others(24): Show |
intron_variant | MODIFIER | c.1029-1294G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442928 | ||||||
chr2:26442956
|
T | C | 4 | a0000c0021t0003g0327a0001c0001t0001g0017a0001c0001t0001g0332others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029-1266T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442956 | ||||||
chr2:26442967
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1029-1255C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442967 | ||||||
chr2:26442985
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1029-1237T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26442985 | ||||||
chr2:26443195
|
T | C | 8 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-1027T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443195 | ||||||
chr2:26443266
|
A | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(2): Show | 5 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029-956A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443266 | ||||||
chr2:26443318
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1029-904A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443318 | ||||||
chr2:26443348
|
G | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0047others(2): Show | 5 | HG01074.hp2 HG01884.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029-874G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443348 | ||||||
chr2:26443380
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1029-842G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443380 | ||||||
chr2:26443529
|
A | G | 1 | a0019c0027t0001g0344 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1029-693A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443529 | ||||||
chr2:26443543
|
T | C | 1 | a0004c0003t0001g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1029-679T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443543 | ||||||
chr2:26443610
|
T | C | 39 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0002g0014others(36): Show | 41 | HG00558.hp2 HG00741.hp2 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.1029-612T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443610 | ||||||
chr2:26443694
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1029-528G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443694 | ||||||
chr2:26443738
|
G | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0007t0001g0270others(5): Show | 8 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-484G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443738 | ||||||
chr2:26443743
|
C | T | 32 | a0001c0007t0001g0092a0001c0007t0001g0251a0001c0007t0002g0293others(29): Show | 32 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1029-479C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443743 | ||||||
chr2:26443819
|
T | C | 363 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(360): Show | 380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.1029-403T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443819 | ||||||
chr2:26443975
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1029-247C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26443975 | ||||||
chr2:26444154
|
G | A | 1 | a0011c0015t0001g0357 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1029-68G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 8/16 | chr2 | 26444154 | ||||||
chr2:26444376
|
C | T | 1 | a0002c0002t0001g0102 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1163+20C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 9/16 | chr2 | 26444376 | ||||||
chr2:26444405
|
C | T | 4 | a0001c0001t0004g0090a0001c0001t0004g0192a0001c0001t0004g0212others(1): Show | 4 | HG00099.hp1 HG03491.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163+49C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 9/16 | chr2 | 26444405 | ||||||
chr2:26444541
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1164-175G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 9/16 | chr2 | 26444541 | ||||||
chr2:26444588
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1164-128G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 9/16 | chr2 | 26444588 | ||||||
chr2:26444626
|
C | T | 1 | a0004c0003t0001g0058 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1164-90C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 9/16 | chr2 | 26444626 | ||||||
chr2:26444644
|
C | T | 11 | a0003c0004t0001g0024a0003c0004t0001g0314a0003c0004t0001g0316others(8): Show | 11 | HG01346.hp2 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1164-72C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 9/16 | chr2 | 26444644 | ||||||
chr2:26445243
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1396+295G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26445243 | ||||||
chr2:26445299
|
G | T | 2 | a0011c0015t0001g0016a0011c0015t0001g0357 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1396+351G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26445299 | ||||||
chr2:26445649
|
G | GTTAT | 8 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0077others(5): Show | 8 | HG01168.hp1 HG02300.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1396+724_1396+727d others(6): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 26445649 | |||||
chr2:26445703
|
G | C | 21 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(18): Show | 22 | HG00408.hp1 HG00609.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1396+755G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26445703 | ||||||
chr2:26445745
|
G | A | 2 | a0011c0015t0001g0016a0011c0015t0001g0357 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1396+797G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26445745 | ||||||
chr2:26445783
|
C | G | 9 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0224others(6): Show | 9 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1396+835C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26445783 | ||||||
chr2:26445790
|
C | A | 1 | a0001c0007t0003g0269 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1396+842C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26445790 | ||||||
chr2:26445922
|
G | T | 94 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(91): Show | 100 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1396+974G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26445922 | ||||||
chr2:26446011
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1396+1063T>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446011 | ||||||
chr2:26446025
|
A | G | 366 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(363): Show | 383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.1396+1077A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446025 | ||||||
chr2:26446094
|
A | AT | 23 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(20): Show | 23 | HG00423.hp1 HG00609.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1396+1168dupT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 26446094 | |||||
chr2:26446094
|
AT | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1396+1168delT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 26446094 | |||||
chr2:26446118
|
A | G | 19 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(16): Show | 19 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.1396+1170A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446118 | ||||||
chr2:26446136
|
G | A | 1 | a0002c0002t0001g0167 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1396+1188G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446136 | ||||||
chr2:26446220
|
C | G | 6 | a0003c0004t0001g0029a0003c0004t0001g0259a0003c0004t0001g0260others(3): Show | 6 | HG01934.hp1 HG02559.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+1272C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446220 | ||||||
chr2:26446223
|
A | T | 1 | a0002c0002t0001g0165 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1396+1275A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446223 | ||||||
chr2:26446405
|
C | T | 6 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396+1457C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446405 | ||||||
chr2:26446408
|
C | T | 1 | a0019c0027t0001g0344 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1396+1460C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446408 | ||||||
chr2:26446409
|
G | A | 1 | a0001c0016t0003g0279 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1396+1461G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446409 | ||||||
chr2:26446535
|
C | T | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1396+1587C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446535 | ||||||
chr2:26446788
|
G | A | 32 | a0001c0007t0001g0092a0001c0007t0001g0251a0001c0007t0002g0293others(29): Show | 32 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1396+1840G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446788 | ||||||
chr2:26446830
|
C | T | 4 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0020others(1): Show | 4 | HG02723.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397-1861C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446830 | ||||||
chr2:26446912
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1397-1779C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26446912 | ||||||
chr2:26447014
|
C | T | 7 | a0003c0004t0001g0328a0003c0004t0001g0329a0003c0004t0003g0264others(4): Show | 8 | HG00642.hp1 HG00738.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1397-1677C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447014 | ||||||
chr2:26447106
|
A | T | 1 | a0019c0027t0001g0344 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1397-1585A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447106 | ||||||
chr2:26447115
|
A | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(46): Show | 53 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1397-1576A>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447115 | ||||||
chr2:26447124
|
AT | A | 2 | a0011c0015t0001g0016a0011c0015t0001g0357 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1397-1566delT | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447124 | ||||||
chr2:26447137
|
G | A | 221 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1397-1554G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447137 | ||||||
chr2:26447189
|
C | T | 4 | a0008c0012t0001g0257a0008c0012t0001g0258a0008c0012t0001g0343others(1): Show | 4 | HG02886.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397-1502C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447189 | ||||||
chr2:26447190
|
G | A | 2 | a0003c0004t0001g0029a0003c0004t0003g0025 | 2 | HG01934.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1397-1501G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447190 | ||||||
chr2:26447205
|
G | A | 21 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(18): Show | 22 | HG00408.hp1 HG00609.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1397-1486G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447205 | ||||||
chr2:26447270
|
G | A | 6 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397-1421G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447270 | ||||||
chr2:26447338
|
G | A | 9 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0224others(6): Show | 9 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1397-1353G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447338 | ||||||
chr2:26447399
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1397-1292C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447399 | ||||||
chr2:26447703
|
A | G | 4 | a0002c0002t0001g0130a0002c0002t0001g0131a0002c0002t0001g0135others(1): Show | 4 | HG00423.hp2 NA18971.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397-988A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447703 | ||||||
chr2:26447812
|
C | T | 1 | a0004c0003t0001g0231 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1397-879C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447812 | ||||||
chr2:26447950
|
C | T | 1 | a0003c0004t0001g0360 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1397-741C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26447950 | ||||||
chr2:26448012
|
T | C | 174 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1397-679T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26448012 | ||||||
chr2:26448089
|
G | A | 1 | a0002c0002t0001g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1397-602G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26448089 | ||||||
chr2:26448157
|
G | A | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1397-534G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26448157 | ||||||
chr2:26448167
|
G | A | 1 | a0007c0009t0001g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1397-524G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26448167 | ||||||
chr2:26448224
|
C | CA | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1397-449dupA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 26448224 | |||||
chr2:26448224
|
C | CAA | 6 | a0001c0001t0001g0052a0001c0001t0001g0204a0001c0007t0001g0144others(3): Show | 6 | HG02074.hp1 HG03209.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397-450_1397-449d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 26448224 | |||||
chr2:26448224
|
CA | C | 16 | a0002c0002t0001g0095a0002c0002t0001g0120a0002c0002t0001g0122others(13): Show | 16 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1397-449delA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 26448224 | |||||
chr2:26448282
|
G | T | 1 | a0006c0008t0001g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1397-409G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26448282 | ||||||
chr2:26448295
|
G | A | 31 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(28): Show | 32 | HG00408.hp1 HG00609.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1397-396G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26448295 | ||||||
chr2:26448357
|
A | G | 1 | a0002c0002t0001g0141 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1397-334A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26448357 | ||||||
chr2:26448459
|
C | T | 1 | a0007c0009t0001g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1397-232C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26448459 | ||||||
chr2:26448467
|
G | A | 8 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0007t0001g0270others(5): Show | 8 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1397-224G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26448467 | ||||||
chr2:26448676
|
A | G | 137 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1397-15A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 10/16 | chr2 | 26448676 | ||||||
chr2:26449146
|
T | G | 81 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0043others(78): Show | 81 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1509+343T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 11/16 | chr2 | 26449146 | ||||||
chr2:26449194
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1509+391C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 11/16 | chr2 | 26449194 | ||||||
chr2:26449249
|
C | A | 31 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(28): Show | 32 | HG00408.hp1 HG00609.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1509+446C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 11/16 | chr2 | 26449249 | ||||||
chr2:26449515
|
C | T | 4 | a0008c0012t0001g0257a0008c0012t0001g0258a0008c0012t0001g0343others(1): Show | 4 | HG02886.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510-481C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 11/16 | chr2 | 26449515 | ||||||
chr2:26449558
|
G | A | 9 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0224others(6): Show | 9 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1510-438G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 11/16 | chr2 | 26449558 | ||||||
chr2:26449730
|
G | A | 1 | a0007c0009t0001g0182 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1510-266G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 11/16 | chr2 | 26449730 | ||||||
chr2:26449826
|
G | A | 6 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1510-170G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 11/16 | chr2 | 26449826 | ||||||
chr2:26449883
|
G | A | 4 | a0002c0002t0001g0086a0002c0002t0001g0093a0002c0002t0001g0094others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-113G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 11/16 | chr2 | 26449883 | ||||||
chr2:26449971
|
G | C | 8 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1510-25G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 11/16 | chr2 | 26449971 | ||||||
chr2:26450389
|
T | C | 2 | a0003c0005t0001g0054a0016c0030t0001g0361 | 2 | HG02647.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1600-203T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 12/16 | chr2 | 26450389 | ||||||
chr2:26450542
|
C | G | 2 | a0001c0007t0003g0266a0001c0007t0003g0269 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1600-50C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 12/16 | chr2 | 26450542 | ||||||
chr2:26450556
|
G | A | 1 | a0002c0002t0001g0150 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1600-36G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 12/16 | chr2 | 26450556 | ||||||
chr2:26450870
|
C | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1689+189C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26450870 | ||||||
chr2:26450910
|
T | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0023others(69): Show | 76 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1689+229T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26450910 | ||||||
chr2:26451002
|
G | A | 20 | a0003c0004t0001g0024a0003c0004t0001g0172a0003c0004t0001g0259others(17): Show | 20 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.1689+321G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451002 | ||||||
chr2:26451052
|
A | G | 1 | a0002c0002t0001g0159 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1689+371A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451052 | ||||||
chr2:26451149
|
C | T | 19 | a0006c0008t0001g0175a0006c0008t0001g0176a0006c0008t0001g0177others(16): Show | 19 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.1689+468C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451149 | ||||||
chr2:26451294
|
G | A | 4 | a0001c0001t0001g0210a0010c0013t0001g0196a0010c0013t0001g0205others(1): Show | 4 | HG00639.hp1 HG01361.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+613G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451294 | ||||||
chr2:26451476
|
G | T | 1 | a0002c0002t0001g0166 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1689+795G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451476 | ||||||
chr2:26451508
|
T | C | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1689+827T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451508 | ||||||
chr2:26451591
|
AAGGTTGA others(20): Show |
A | 9 | a0001c0007t0003g0269a0008c0011t0001g0323a0008c0011t0001g0324others(6): Show | 9 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1689+937_1689+963d others(29): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 26451591 | |||||
chr2:26451706
|
A | G | 1 | a0003c0004t0001g0342 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1689+1025A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451706 | ||||||
chr2:26451735
|
T | C | 1 | a0006c0008t0001g0180 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1689+1054T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451735 | ||||||
chr2:26451760
|
G | C | 1 | a0002c0002t0001g0165 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1689+1079G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451760 | ||||||
chr2:26451774
|
A | G | 1 | a0004c0029t0001g0109 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1689+1093A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451774 | ||||||
chr2:26451836
|
G | A | 4 | a0008c0012t0001g0257a0008c0012t0001g0258a0008c0012t0001g0343others(1): Show | 4 | HG02886.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+1155G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451836 | ||||||
chr2:26451982
|
G | A | 8 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG01943.hp1 HG01975.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.1689+1301G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26451982 | ||||||
chr2:26452004
|
C | T | 1 | a0002c0002t0001g0165 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1690-1316C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452004 | ||||||
chr2:26452016
|
C | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-1304C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452016 | ||||||
chr2:26452092
|
G | A | 1 | a0004c0003t0001g0256 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1690-1228G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452092 | ||||||
chr2:26452093
|
C | CA | 7 | a0002c0002t0001g0101a0002c0002t0001g0125a0002c0002t0001g0151others(4): Show | 8 | HG01243.hp2 HG02559.hp2 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.1690-1214dupA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 26452093 | |||||
chr2:26452093
|
CA | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1690-1214delA | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 26452093 | |||||
chr2:26452093
|
CAA | C | 20 | a0004c0003t0001g0229a0006c0008t0001g0175a0006c0008t0001g0176others(17): Show | 20 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.1690-1215_1690-121 others(6): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 26452093 | |||||
chr2:26452108
|
C | T | 1 | a0007c0009t0001g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1690-1212C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452108 | ||||||
chr2:26452136
|
G | A | 1 | a0006c0008t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1690-1184G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452136 | ||||||
chr2:26452266
|
T | C | 1 | a0003c0004t0003g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1690-1054T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452266 | ||||||
chr2:26452281
|
A | G | 1 | a0004c0003t0001g0218 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1690-1039A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452281 | ||||||
chr2:26452288
|
C | T | 66 | a0000c0021t0003g0327a0001c0001t0001g0021a0001c0001t0001g0023others(63): Show | 68 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1690-1032C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452288 | ||||||
chr2:26452343
|
T | C | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-977T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452343 | ||||||
chr2:26452421
|
G | A | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-899G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452421 | ||||||
chr2:26452479
|
C | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-841C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452479 | ||||||
chr2:26452490
|
C | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-830C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452490 | ||||||
chr2:26452599
|
G | C | 2 | a0011c0015t0001g0016a0011c0015t0001g0357 | 3 | HG01243.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1690-721G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452599 | ||||||
chr2:26452610
|
G | A | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-710G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452610 | ||||||
chr2:26452637
|
A | G | 9 | a0007c0009t0001g0128a0007c0009t0001g0174a0007c0009t0001g0182others(6): Show | 9 | HG00609.hp2 HG02135.hp1 HG04199.hp1 others(6): Show |
intron_variant | MODIFIER | c.1690-683A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452637 | ||||||
chr2:26452686
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1690-634C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452686 | ||||||
chr2:26452747
|
G | A | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-573G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452747 | ||||||
chr2:26452750
|
C | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-570C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452750 | ||||||
chr2:26452751
|
C | G | 1 | a0011c0015t0001g0016 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1690-569C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452751 | ||||||
chr2:26452792
|
T | C | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-528T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452792 | ||||||
chr2:26452811
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1690-509T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452811 | ||||||
chr2:26452929
|
C | A | 9 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0224others(6): Show | 9 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1690-391C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452929 | ||||||
chr2:26452999
|
A | C | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1690-321A>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26452999 | ||||||
chr2:26453071
|
G | A | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-249G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26453071 | ||||||
chr2:26453086
|
A | G | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-234A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 13/16 | chr2 | 26453086 | ||||||
chr2:26453758
|
C | T | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1919+209C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26453758 | ||||||
chr2:26453763
|
C | G | 1 | a0005c0006t0001g0238 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1919+214C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26453763 | ||||||
chr2:26453864
|
A | G | 8 | a0008c0011t0001g0323a0008c0011t0001g0324a0008c0011t0001g0333others(5): Show | 8 | HG00733.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1919+315A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26453864 | ||||||
chr2:26453886
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1919+337C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26453886 | ||||||
chr2:26454134
|
G | A | 1 | a0020c0026t0001g0114 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1920-513G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26454134 | ||||||
chr2:26454172
|
G | A | 6 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1920-475G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26454172 | ||||||
chr2:26454346
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1920-301G>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26454346 | ||||||
chr2:26454376
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1920-271G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26454376 | ||||||
chr2:26454427
|
T | G | 8 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0224others(5): Show | 8 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1920-220T>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26454427 | ||||||
chr2:26454435
|
G | T | 253 | a0000c0021t0003g0327a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1920-212G>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26454435 | ||||||
chr2:26454458
|
C | T | 1 | a0008c0011t0005g0310 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1920-189C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26454458 | ||||||
chr2:26454459
|
G | A | 13 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0071others(10): Show | 13 | HG00741.hp2 HG01258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1920-188G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26454459 | ||||||
chr2:26454467
|
C | T | 74 | a0000c0021t0003g0327a0001c0001t0001g0021a0001c0001t0001g0023others(71): Show | 76 | HG00099.hp1 HG00558.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1920-180C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 14/16 | chr2 | 26454467 | ||||||
chr2:26454816
|
A | G | 1 | a0003c0004t0001g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2063+26A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 15/16 | chr2 | 26454816 | ||||||
chr2:26454861
|
G | A | 22 | a0003c0004t0001g0024a0003c0004t0001g0029a0003c0004t0001g0107others(19): Show | 22 | HG00609.hp1 HG01346.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.2063+71G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 15/16 | chr2 | 26454861 | ||||||
chr2:26454942
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 161 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.2063+152A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 15/16 | chr2 | 26454942 | ||||||
chr2:26455266
|
G | A | 9 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(6): Show | 10 | HG00738.hp1 HG00741.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2166+33G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455266 | ||||||
chr2:26455301
|
G | A | 110 | a0001c0007t0001g0144a0001c0007t0002g0293a0002c0002t0001g0001others(107): Show | 118 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.2166+68G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455301 | ||||||
chr2:26455325
|
C | A | 14 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0041others(11): Show | 14 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2166+92C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455325 | ||||||
chr2:26455429
|
A | G | 8 | a0001c0001t0001g0332a0001c0016t0003g0280a0003c0004t0001g0262others(5): Show | 8 | HG01106.hp1 HG01496.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2166+196A>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455429 | ||||||
chr2:26455602
|
G | A | 1 | a0001c0007t0002g0295 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2166+369G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455602 | ||||||
chr2:26455628
|
C | A | 227 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0021others(224): Show | 239 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.2166+395C>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455628 | ||||||
chr2:26455648
|
C | G | 5 | a0001c0016t0003g0278a0001c0016t0003g0279a0001c0016t0003g0280others(2): Show | 5 | HG02486.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2166+415C>G | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455648 | ||||||
chr2:26455663
|
G | A | 1 | a0002c0002t0001g0142 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2166+430G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455663 | ||||||
chr2:26455705
|
T | C | 2 | a0002c0002t0001g0145a0002c0002t0001g0149 | 2 | HG03834.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.2166+472T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455705 | ||||||
chr2:26455922
|
G | A | 123 | a0000c0021t0003g0327a0001c0001t0001g0021a0001c0001t0001g0023others(120): Show | 129 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.2167-539G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455922 | ||||||
chr2:26455940
|
CGT | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(330): Show | 350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.2167-517_2167-516d others(4): Show |
DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 26455940 | |||||
chr2:26455943
|
G | A | 1 | a0005c0006t0001g0238 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2167-518G>A | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26455943 | ||||||
chr2:26456109
|
C | T | 27 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0338others(24): Show | 27 | HG00099.hp1 HG00733.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2167-352C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26456109 | ||||||
chr2:26456141
|
T | C | 1 | a0002c0002t0001g0146 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2167-320T>C | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26456141 | ||||||
chr2:26456396
|
C | T | 1 | a0001c0001t0007g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2167-65C>T | DRC1 | ENSG00000157856.12 | transcript | ENST00000288710.7 | protein_coding | 16/16 | chr2 | 26456396 |