geneid | 164781 |
---|---|
ensemblid | ENSG00000123977.10 |
hgncid | 26383 |
symbol | DAW1 |
name | dynein assembly factor with WD repeats 1 |
refseq_nuc | NM_178821.3 |
refseq_prot | NP_849143.1 |
ensembl_nuc | ENST00000309931.3 |
ensembl_prot | ENSP00000311899.2 |
mane_status | MANE Select |
chr | chr2 |
start | 227871631 |
end | 227924344 |
strand | + |
ver | v1.2 |
region | chr2:227871631-227924344 |
region5000 | chr2:227866631-227929344 |
regionname0 | DAW1_chr2_227871631_227924344 |
regionname5000 | DAW1_chr2_227866631_227929344 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 415 | 284 | 54 | 48 | 144 | 8 | 28 | 111 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0002 | 0/0 | 415 | 36 | 15 | 12 | 0 | 4 | 5 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0003 | 0/0 | 415 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0004 | 0/0 | 415 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0005 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0006 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0007 | 0/0 | 415 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0008 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0009 | 0/0 | 415 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0010 | 0/0 | 415 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1248 | 251 | 43 | 44 | 130 | 7 | 25 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0002 | 0/0 | 1248 | 36 | 15 | 12 | 0 | 4 | 5 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0003 | 0/0 | 1248 | 31 | 10 | 4 | 14 | 1 | 2 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0004 | 0/0 | 1248 | 12 | 12 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0005 | 0/0 | 1248 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0006 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0007 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0008 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0009 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0010 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0011 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0012 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
c0013 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 436 | 315 | 83 | 56 | 132 | 11 | 31 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
t0002 | 0/0 | 436 | 21 | 1 | 4 | 14 | 1 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
t0003 | 0/0 | 436 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
t0004 | 0/0 | 436 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
t0005 | 0/0 | 436 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1248 | 251 | 43 | 44 | 130 | 7 | 25 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0001c0003 | 0/0 | 1248 | 31 | 10 | 4 | 14 | 1 | 2 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0001c0012 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0001c0013 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0002c0002 | 0/0 | 1248 | 36 | 15 | 12 | 0 | 4 | 5 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0003c0004 | 0/0 | 1248 | 12 | 12 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0004c0005 | 0/0 | 1248 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0005c0011 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0006c0010 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0007c0009 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0008c0008 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0009c0007 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0010c0006 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1683 | 250 | 43 | 44 | 130 | 7 | 24 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0001c0001t0005 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0001c0003t0001 | 0/0 | 1683 | 10 | 9 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0001c0003t0002 | 0/0 | 1683 | 21 | 1 | 4 | 14 | 1 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0001c0012t0001 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0001c0013t0001 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0002c0002t0001 | 0/0 | 1683 | 35 | 15 | 12 | 0 | 4 | 4 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0002c0002t0004 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0003c0004t0001 | 0/0 | 1683 | 12 | 12 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0004c0005t0003 | 0/0 | 1683 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0005c0011t0001 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0006c0010t0001 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0007c0009t0001 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0008c0008t0001 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0009c0007t0001 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
a0010c0006t0001 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | copy fasta | chr2 | 227866631 | 227929344 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0012t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0001c0013t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0002c0002t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0003c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0004c0005t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0004c0005t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0005c0011t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0006c0010t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0007c0009t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0008c0008t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0009c0007t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
a0010c0006t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0027 | EUR | GBR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0029 | EUR | FIN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00438 | hp1 | a0004 | c0005 | t0003 | g0322 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00438 | hp2 | a0001 | c0003 | t0002 | g0156 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00642 | hp1 | a0001 | c0003 | t0002 | g0165 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG00738 | hp2 | a0001 | c0003 | t0002 | g0167 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01243 | hp2 | a0001 | c0003 | t0002 | g0168 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0148 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0291 | EUR | IBS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0020 | EUR | IBS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0157 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0316 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02055 | hp2 | a0003 | c0004 | t0001 | g0313 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02132 | hp1 | a0001 | c0003 | t0002 | g0182 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02258 | hp1 | a0006 | c0010 | t0001 | g0149 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02280 | hp2 | a0003 | c0004 | t0001 | g0312 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02293 | hp1 | a0001 | c0003 | t0002 | g0164 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02572 | hp1 | a0003 | c0004 | t0001 | g0318 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02602 | hp1 | a0007 | c0009 | t0001 | g0117 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0147 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02630 | hp1 | a0003 | c0004 | t0001 | g0311 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0297 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02723 | hp2 | a0008 | c0008 | t0001 | g0323 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02735 | hp2 | a0001 | c0003 | t0002 | g0181 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0303 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0163 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0314 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0307 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0298 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0306 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02970 | hp1 | a0001 | c0012 | t0001 | g0070 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02970 | hp2 | a0003 | c0004 | t0001 | g0319 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02976 | hp1 | a0005 | c0011 | t0001 | g0299 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02976 | hp2 | a0003 | c0004 | t0001 | g0308 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03130 | hp2 | a0003 | c0004 | t0001 | g0309 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03195 | hp1 | a0003 | c0004 | t0001 | g0310 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0300 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03453 | hp2 | a0003 | c0004 | t0001 | g0315 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03486 | hp2 | a0003 | c0004 | t0001 | g0317 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03540 | hp2 | a0003 | c0004 | t0001 | g0320 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0146 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0031 | SAS | BEB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG04184 | hp2 | a0001 | c0013 | t0001 | g0249 | SAS | BEB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0152 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG04204 | hp1 | a0002 | c0002 | t0004 | g0150 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0301 | AFR | YRI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18940 | hp1 | a0001 | c0003 | t0002 | g0177 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18943 | hp2 | a0001 | c0003 | t0002 | g0154 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0170 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18946 | hp1 | a0001 | c0003 | t0002 | g0173 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18956 | hp1 | a0001 | c0003 | t0002 | g0175 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18968 | hp1 | a0009 | c0007 | t0001 | g0288 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18973 | hp2 | a0001 | c0003 | t0002 | g0174 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18979 | hp2 | a0004 | c0005 | t0003 | g0321 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18993 | hp1 | a0001 | c0003 | t0002 | g0172 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18998 | hp1 | a0001 | c0003 | t0002 | g0153 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19054 | hp2 | a0001 | c0003 | t0002 | g0155 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19068 | hp1 | a0001 | c0003 | t0002 | g0178 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19074 | hp2 | a0010 | c0006 | t0001 | g0287 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19082 | hp1 | a0001 | c0003 | t0002 | g0171 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19086 | hp1 | a0001 | c0003 | t0002 | g0169 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA20129 | hp1 | a0003 | c0004 | t0001 | g0305 | AFR | ASW | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0302 | AFR | ASW | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | TSI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA20805 | hp2 | a0001 | c0003 | t0002 | g0166 | EUR | TSI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | GIH | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | USA | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | USA | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | LWK | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0262 | REF | REF | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0063 | REF | REF | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:227871709
|
T | C | 1 | a0010 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.20T>C | p.Leu7Pro | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/13 | 79/1683 | 20/1248 | 7/415 | chr2 | 227871709 | ||
chr2:227885390
|
C | T | 1 | a0003 | 12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
missense_variant | MODERATE | c.80C>T | p.Thr27Ile | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/13 | 139/1683 | 80/1248 | 27/415 | chr2 | 227885390 | ||
chr2:227893796
|
T | G | 2 | a0009a0010 | 2 | NA18968.hp1 NA19074.hp2 |
missense_variant&splice_region_variant | MODERATE | c.319T>G | p.Phe107Val | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/13 | 378/1683 | 319/1248 | 107/415 | chr2 | 227893796 | ||
chr2:227893821
|
C | T | 1 | a0005 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.344C>T | p.Thr115Met | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/13 | 403/1683 | 344/1248 | 115/415 | chr2 | 227893821 | ||
chr2:227893838
|
A | T | 2 | a0002a0006 | 37 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
missense_variant | MODERATE | c.361A>T | p.Thr121Ser | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/13 | 420/1683 | 361/1248 | 121/415 | chr2 | 227893838 | ||
chr2:227893839
|
C | T | 1 | a0004 | 2 | HG00438.hp1 NA18979.hp2 |
missense_variant | MODERATE | c.362C>T | p.Thr121Ile | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/13 | 421/1683 | 362/1248 | 121/415 | chr2 | 227893839 | ||
chr2:227898271
|
C | T | 1 | a0006 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.530C>T | p.Thr177Ile | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/13 | 589/1683 | 530/1248 | 177/415 | chr2 | 227898271 | ||
chr2:227906255
|
G | A | 1 | a0008 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.775G>A | p.Gly259Ser | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/13 | 834/1683 | 775/1248 | 259/415 | chr2 | 227906255 | ||
chr2:227923964
|
G | A | 1 | a0007 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1244G>A | p.Arg415His | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 13/13 | 1303/1683 | 1244/1248 | 415/415 | chr2 | 227923964 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:227871710
|
G | T | 1 | a0001c0013 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.21G>T | p.Leu7Leu | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/13 | 80/1683 | 21/1248 | 7/415 | chr2 | 227871710 | ||
chr2:227889877
|
A | G | 1 | a0001c0012 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.135A>G | p.Val45Val | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/13 | 194/1683 | 135/1248 | 45/415 | chr2 | 227889877 | ||
chr2:227893864
|
G | C | 2 | a0001c0003a0005c0011 | 32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
synonymous_variant | LOW | c.387G>C | p.Thr129Thr | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/13 | 446/1683 | 387/1248 | 129/415 | chr2 | 227893864 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:227871666
|
G | C | 1 | a0004c0005t0003 | 2 | HG00438.hp1 NA18979.hp2 |
5_prime_UTR_variant | MODIFIER | c.-24G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/13 | 24 | chr2 | 227871666 | |||||
chr2:227924006
|
T | C | 1 | a0001c0003t0002 | 21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*38T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 13/13 | 38 | chr2 | 227924006 | |||||
chr2:227924085
|
A | G | 1 | a0001c0001t0005 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*117A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 13/13 | 117 | chr2 | 227924085 | |||||
chr2:227924254
|
A | G | 1 | a0002c0002t0004 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 13/13 | 286 | chr2 | 227924254 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:227871778
|
C | G | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | NA18979.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.40+49C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227871778 | ||||||
chr2:227871811
|
A | G | 141 | a0001c0001t0001g0012a0001c0001t0001g0186a0001c0001t0001g0187others(138): Show | 142 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.40+82A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227871811 | ||||||
chr2:227871849
|
A | C | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40+120A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227871849 | ||||||
chr2:227871892
|
C | T | 141 | a0001c0001t0001g0012a0001c0001t0001g0186a0001c0001t0001g0187others(138): Show | 142 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.40+163C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227871892 | ||||||
chr2:227871999
|
A | C | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+270A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227871999 | ||||||
chr2:227872097
|
G | C | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40+368G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872097 | ||||||
chr2:227872110
|
T | C | 17 | a0001c0001t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(14): Show | 17 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.40+381T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872110 | ||||||
chr2:227872137
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40+408C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872137 | ||||||
chr2:227872275
|
C | CA | 28 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(25): Show | 28 | HG00423.hp2 HG01106.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.40+563dupA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227872275 | |||||
chr2:227872290
|
AAAG | A | 10 | a0001c0003t0001g0306a0001c0003t0001g0307a0003c0004t0001g0305others(7): Show | 10 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.40+564_40+566delGA others(1): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227872290 | |||||
chr2:227872292
|
AG | A | 112 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0199others(109): Show | 113 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.40+564delG | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872292 | ||||||
chr2:227872293
|
G | A | 13 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(10): Show | 13 | HG00323.hp1 HG01123.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.40+564G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872293 | ||||||
chr2:227872297
|
A | G | 138 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0187others(135): Show | 139 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.40+568A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872297 | ||||||
chr2:227872400
|
G | T | 1 | a0001c0001t0001g0185 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.40+671G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872400 | ||||||
chr2:227872531
|
T | C | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+802T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872531 | ||||||
chr2:227872584
|
C | T | 1 | a0001c0003t0001g0316 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.40+855C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872584 | ||||||
chr2:227872586
|
A | G | 1 | a0002c0002t0001g0184 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.40+857A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872586 | ||||||
chr2:227872649
|
T | C | 1 | a0001c0001t0001g0004 | 2 | NA18939.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.40+920T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872649 | ||||||
chr2:227872693
|
C | T | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+964C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872693 | ||||||
chr2:227872713
|
C | T | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40+984C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872713 | ||||||
chr2:227872726
|
C | G | 1 | a0001c0001t0001g0304 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.40+997C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872726 | ||||||
chr2:227872794
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.40+1065G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872794 | ||||||
chr2:227872977
|
A | G | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+1248A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872977 | ||||||
chr2:227872979
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.40+1250G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872979 | ||||||
chr2:227873200
|
C | T | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+1471C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873200 | ||||||
chr2:227873250
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.40+1521A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873250 | ||||||
chr2:227873276
|
T | C | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+1547T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873276 | ||||||
chr2:227873338
|
T | C | 117 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(114): Show | 118 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.40+1609T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873338 | ||||||
chr2:227873427
|
G | A | 1 | a0001c0001t0005g0031 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.40+1698G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873427 | ||||||
chr2:227873456
|
A | G | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40+1727A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873456 | ||||||
chr2:227873549
|
G | A | 1 | a0001c0003t0001g0316 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.40+1820G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873549 | ||||||
chr2:227873552
|
C | A | 116 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(113): Show | 117 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.40+1823C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873552 | ||||||
chr2:227873585
|
C | T | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+1856C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873585 | ||||||
chr2:227873598
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40+1869G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873598 | ||||||
chr2:227873618
|
T | C | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+1889T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873618 | ||||||
chr2:227873672
|
A | T | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+1943A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873672 | ||||||
chr2:227873861
|
A | G | 2 | a0003c0004t0001g0319a0003c0004t0001g0320 | 2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.40+2132A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873861 | ||||||
chr2:227873889
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.40+2160C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873889 | ||||||
chr2:227873967
|
C | T | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+2238C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873967 | ||||||
chr2:227874007
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40+2278G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874007 | ||||||
chr2:227874016
|
G | T | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+2287G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874016 | ||||||
chr2:227874073
|
ATAATTTT others(14): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40+2346_40+2366del others(21): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874073 | |||||
chr2:227874156
|
T | C | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+2427T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874156 | ||||||
chr2:227874206
|
C | T | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+2477C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874206 | ||||||
chr2:227874244
|
A | G | 13 | a0001c0003t0001g0316a0001c0003t0002g0314a0003c0004t0001g0308others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.40+2515A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874244 | ||||||
chr2:227874284
|
A | G | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+2555A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874284 | ||||||
chr2:227874330
|
T | G | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40+2601T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874330 | ||||||
chr2:227874419
|
G | T | 202 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0030others(199): Show | 206 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.40+2690G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874419 | ||||||
chr2:227874438
|
G | A | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+2709G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874438 | ||||||
chr2:227874457
|
A | G | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+2728A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874457 | ||||||
chr2:227874652
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.40+2923C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874652 | ||||||
chr2:227874742
|
A | C | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(320): Show | 338 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.40+3013A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874742 | ||||||
chr2:227874742
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.40+3013A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874742 | ||||||
chr2:227874758
|
C | T | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40+3029C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874758 | ||||||
chr2:227874833
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | NA18939.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.40+3104C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874833 | ||||||
chr2:227874845
|
C | T | 6 | a0001c0001t0001g0197a0001c0001t0001g0289a0001c0001t0001g0290others(3): Show | 6 | HG00323.hp1 HG00735.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+3116C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874845 | ||||||
chr2:227874890
|
G | C | 3 | a0001c0003t0001g0297a0001c0003t0001g0306a0001c0003t0001g0307 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40+3161G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874890 | ||||||
chr2:227874963
|
A | AAAAC | 88 | a0001c0001t0001g0013a0001c0001t0001g0059a0001c0001t0001g0062others(85): Show | 88 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.40+3256_40+3259dup others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874963 | |||||
chr2:227874963
|
A | AAAACAAA others(1): Show |
37 | a0001c0001t0001g0196a0001c0001t0001g0267a0001c0001t0001g0268others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.40+3252_40+3259dup others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874963 | |||||
chr2:227874963
|
A | AAAACAAA others(5): Show |
35 | a0001c0001t0001g0030a0001c0001t0001g0176a0001c0001t0001g0179others(32): Show | 37 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.40+3248_40+3259dup others(12): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874963 | |||||
chr2:227874963
|
A | AAAACAAA others(9): Show |
14 | a0001c0003t0001g0152a0001c0003t0002g0153a0001c0003t0002g0154others(11): Show | 15 | HG00438.hp2 HG00642.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.40+3244_40+3259dup others(16): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874963 | |||||
chr2:227874987
|
CAGAA | C | 9 | a0001c0001t0001g0187a0001c0003t0001g0297a0001c0003t0001g0298others(6): Show | 9 | HG02717.hp1 HG02723.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+3260_40+3263del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874987 | |||||
chr2:227874989
|
G | A | 132 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(129): Show | 133 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40+3260G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874989 | ||||||
chr2:227874991
|
A | C | 131 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(128): Show | 132 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.40+3262A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874991 | ||||||
chr2:227875067
|
G | A | 35 | a0001c0003t0001g0297a0002c0002t0001g0003a0002c0002t0001g0011others(32): Show | 38 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.40+3338G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875067 | ||||||
chr2:227875069
|
A | G | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+3340A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875069 | ||||||
chr2:227875078
|
G | A | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+3349G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875078 | ||||||
chr2:227875266
|
T | C | 23 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0003t0001g0152others(20): Show | 23 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.40+3537T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875266 | ||||||
chr2:227875395
|
T | C | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+3666T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875395 | ||||||
chr2:227875411
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40+3682C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875411 | ||||||
chr2:227875762
|
A | G | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+4033A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875762 | ||||||
chr2:227876020
|
CT | C | 26 | a0001c0001t0001g0012a0001c0001t0001g0066a0001c0001t0001g0197others(23): Show | 27 | HG00323.hp1 HG00735.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.40+4304delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227876020 | |||||
chr2:227876020
|
CTT | C | 118 | a0001c0001t0001g0013a0001c0001t0001g0059a0001c0001t0001g0062others(115): Show | 118 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.40+4303_40+4304del others(2): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227876020 | |||||
chr2:227876025
|
TTTTTTTT others(50): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.40+4299_40+4355del others(57): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227876025 | |||||
chr2:227876030
|
T | G | 20 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0200others(17): Show | 20 | HG01361.hp1 HG01981.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.40+4301T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876030 | ||||||
chr2:227876065
|
T | C | 11 | a0003c0004t0001g0308a0003c0004t0001g0309a0003c0004t0001g0310others(8): Show | 11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.40+4336T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876065 | ||||||
chr2:227876181
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.40+4452A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876181 | ||||||
chr2:227876186
|
A | T | 119 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(116): Show | 120 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.40+4457A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876186 | ||||||
chr2:227876211
|
G | A | 152 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(149): Show | 154 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.40+4482G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876211 | ||||||
chr2:227876253
|
C | A | 1 | a0003c0004t0001g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.40+4524C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876253 | ||||||
chr2:227876295
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.40+4566C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876295 | ||||||
chr2:227876342
|
C | T | 1 | a0002c0002t0001g0151 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.40+4613C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876342 | ||||||
chr2:227876534
|
T | A | 119 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(116): Show | 120 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.40+4805T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876534 | ||||||
chr2:227876565
|
A | T | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.40+4836A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876565 | ||||||
chr2:227876581
|
G | C | 14 | a0001c0003t0001g0316a0001c0003t0002g0314a0003c0004t0001g0305others(11): Show | 14 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.40+4852G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876581 | ||||||
chr2:227876621
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.40+4892C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876621 | ||||||
chr2:227876642
|
C | T | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.40+4913C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876642 | ||||||
chr2:227876718
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+4989T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876718 | ||||||
chr2:227876725
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+4996G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876725 | ||||||
chr2:227876754
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0143a0001c0001t0001g0144 | 4 | HG02451.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+5025C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876754 | ||||||
chr2:227876860
|
G | T | 1 | a0002c0002t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.40+5131G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876860 | ||||||
chr2:227877210
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.40+5481G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877210 | ||||||
chr2:227877277
|
C | T | 1 | a0002c0002t0004g0150 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.40+5548C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877277 | ||||||
chr2:227877376
|
C | T | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+5647C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877376 | ||||||
chr2:227877505
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.40+5776T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877505 | ||||||
chr2:227877506
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.40+5777A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877506 | ||||||
chr2:227877579
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.40+5850G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877579 | ||||||
chr2:227877677
|
G | A | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.40+5948G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877677 | ||||||
chr2:227877769
|
C | G | 1 | a0001c0003t0002g0181 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.40+6040C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877769 | ||||||
chr2:227877798
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.40+6069G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877798 | ||||||
chr2:227877809
|
C | T | 2 | a0001c0001t0001g0062a0008c0008t0001g0323 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.40+6080C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877809 | ||||||
chr2:227877827
|
G | C | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40+6098G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877827 | ||||||
chr2:227877854
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.40+6125A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877854 | ||||||
chr2:227877929
|
C | T | 257 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(254): Show | 265 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.40+6200C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877929 | ||||||
chr2:227878073
|
T | C | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | NA18979.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.40+6344T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878073 | ||||||
chr2:227878153
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40+6424A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878153 | ||||||
chr2:227878554
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.41-6797T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878554 | ||||||
chr2:227878632
|
G | T | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-6719G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878632 | ||||||
chr2:227878656
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(44): Show | 52 | HG00099.hp2 HG00621.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.41-6695C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878656 | ||||||
chr2:227878679
|
G | T | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-6672G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878679 | ||||||
chr2:227878760
|
AT | A | 257 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(254): Show | 265 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.41-6584delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227878760 | |||||
chr2:227878809
|
ATTTT | A | 142 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(139): Show | 143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.41-6528_41-6525del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227878809 | |||||
chr2:227878827
|
G | T | 1 | a0001c0001t0001g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.41-6524G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878827 | ||||||
chr2:227878917
|
A | G | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.41-6434A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878917 | ||||||
chr2:227878945
|
T | C | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-6406T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878945 | ||||||
chr2:227879030
|
C | T | 1 | a0001c0003t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.41-6321C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879030 | ||||||
chr2:227879051
|
A | G | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-6300A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879051 | ||||||
chr2:227879202
|
A | G | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-6149A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879202 | ||||||
chr2:227879207
|
G | A | 1 | a0002c0002t0001g0157 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.41-6144G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879207 | ||||||
chr2:227879344
|
T | C | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-6007T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879344 | ||||||
chr2:227879428
|
T | G | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-5923T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879428 | ||||||
chr2:227879609
|
C | T | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-5742C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879609 | ||||||
chr2:227879871
|
T | G | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-5480T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879871 | ||||||
chr2:227880020
|
G | A | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.41-5331G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880020 | ||||||
chr2:227880046
|
G | A | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-5305G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880046 | ||||||
chr2:227880275
|
C | A | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-5076C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880275 | ||||||
chr2:227880293
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(263): Show | 275 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.41-5058G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880293 | ||||||
chr2:227880342
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.41-5009T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880342 | ||||||
chr2:227880360
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.41-4991G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880360 | ||||||
chr2:227880367
|
A | G | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-4984A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880367 | ||||||
chr2:227880381
|
CT | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0056a0001c0001t0001g0060others(8): Show | 12 | HG01358.hp2 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.41-4954delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227880381 | |||||
chr2:227880381
|
CTT | C | 125 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(122): Show | 126 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.41-4955_41-4954del others(2): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227880381 | |||||
chr2:227880381
|
CTTT | C | 11 | a0003c0004t0001g0308a0003c0004t0001g0309a0003c0004t0001g0310others(8): Show | 11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.41-4956_41-4954del others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227880381 | |||||
chr2:227880470
|
C | G | 23 | a0001c0003t0001g0297a0001c0003t0001g0298a0001c0003t0001g0300others(20): Show | 23 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.41-4881C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880470 | ||||||
chr2:227880671
|
A | G | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-4680A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880671 | ||||||
chr2:227880698
|
C | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA18942.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.41-4653C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880698 | ||||||
chr2:227880730
|
C | T | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-4621C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880730 | ||||||
chr2:227880927
|
A | G | 1 | a0002c0002t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.41-4424A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880927 | ||||||
chr2:227881024
|
G | A | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-4327G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881024 | ||||||
chr2:227881165
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.41-4186G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881165 | ||||||
chr2:227881193
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0142 | 4 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-4158A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881193 | ||||||
chr2:227881357
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | NA19074.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.41-3994A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881357 | ||||||
chr2:227881403
|
G | A | 23 | a0001c0003t0001g0297a0001c0003t0001g0298a0001c0003t0001g0300others(20): Show | 23 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.41-3948G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881403 | ||||||
chr2:227881418
|
G | A | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.41-3933G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881418 | ||||||
chr2:227881439
|
A | G | 1 | a0002c0002t0001g0162 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41-3912A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881439 | ||||||
chr2:227881628
|
C | T | 1 | a0001c0003t0002g0181 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.41-3723C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881628 | ||||||
chr2:227881698
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41-3653G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881698 | ||||||
chr2:227881743
|
C | CT | 65 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(62): Show | 68 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.41-3581dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227881743 | |||||
chr2:227881743
|
CT | C | 24 | a0001c0001t0001g0037a0001c0001t0001g0111a0001c0001t0001g0176others(21): Show | 24 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-3581delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227881743 | |||||
chr2:227881743
|
CTTT | C | 12 | a0001c0001t0001g0186a0001c0001t0001g0194a0001c0001t0001g0198others(9): Show | 12 | HG02717.hp1 HG02809.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.41-3583_41-3581del others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227881743 | |||||
chr2:227881743
|
CTTTT | C | 109 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(106): Show | 110 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.41-3584_41-3581del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227881743 | |||||
chr2:227881743
|
CTTTTT | C | 19 | a0001c0001t0001g0062a0001c0001t0001g0226a0001c0001t0001g0227others(16): Show | 19 | HG01099.hp2 HG01496.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-3585_41-3581del others(5): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227881743 | |||||
chr2:227881751
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.41-3600T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881751 | ||||||
chr2:227881813
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.41-3538T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881813 | ||||||
chr2:227881816
|
A | G | 117 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(114): Show | 118 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.41-3535A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881816 | ||||||
chr2:227881833
|
A | G | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-3518A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881833 | ||||||
chr2:227881924
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.41-3427G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881924 | ||||||
chr2:227881967
|
A | G | 257 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(254): Show | 265 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.41-3384A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881967 | ||||||
chr2:227882160
|
T | G | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-3191T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882160 | ||||||
chr2:227882336
|
G | A | 144 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(141): Show | 145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41-3015G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882336 | ||||||
chr2:227882383
|
C | T | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-2968C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882383 | ||||||
chr2:227882450
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.41-2901T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882450 | ||||||
chr2:227882451
|
C | T | 1 | a0002c0002t0001g0162 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41-2900C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882451 | ||||||
chr2:227882927
|
T | C | 1 | a0002c0002t0001g0003 | 3 | HG01069.hp1 HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.41-2424T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882927 | ||||||
chr2:227883419
|
G | A | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.41-1932G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883419 | ||||||
chr2:227883463
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0142 | 4 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-1888T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883463 | ||||||
chr2:227883633
|
T | C | 162 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(159): Show | 163 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.41-1718T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883633 | ||||||
chr2:227883637
|
T | C | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.41-1714T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883637 | ||||||
chr2:227883675
|
A | C | 1 | a0001c0001t0001g0139 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.41-1676A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883675 | ||||||
chr2:227883707
|
G | A | 4 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0024others(1): Show | 4 | HG01884.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-1644G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883707 | ||||||
chr2:227883771
|
T | C | 1 | a0003c0004t0001g0313 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.41-1580T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883771 | ||||||
chr2:227883949
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.41-1402T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883949 | ||||||
chr2:227883972
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.41-1379G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883972 | ||||||
chr2:227884288
|
C | A | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-1063C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227884288 | ||||||
chr2:227884381
|
A | G | 1 | a0001c0001t0001g0007 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.41-970A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227884381 | ||||||
chr2:227884562
|
G | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 59 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.41-789G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227884562 | ||||||
chr2:227884862
|
G | T | 1 | a0001c0001t0001g0254 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.41-489G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227884862 | ||||||
chr2:227885019
|
C | A | 117 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(114): Show | 118 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.41-332C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885019 | ||||||
chr2:227885039
|
G | A | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(160): Show | 164 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.41-312G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885039 | ||||||
chr2:227885052
|
T | C | 119 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(116): Show | 120 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.41-299T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885052 | ||||||
chr2:227885080
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0179 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.41-271A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885080 | ||||||
chr2:227885120
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.41-231T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885120 | ||||||
chr2:227885131
|
A | G | 1 | a0002c0002t0001g0161 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.41-220A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885131 | ||||||
chr2:227885304
|
AG | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0144 | 3 | HG02451.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.41-45delG | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227885304 | |||||
chr2:227885523
|
G | T | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(160): Show | 164 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.113+100G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227885523 | ||||||
chr2:227885594
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.113+171T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227885594 | ||||||
chr2:227885651
|
T | TA | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(160): Show | 164 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.113+235dupA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227885651 | |||||
chr2:227885783
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.113+360C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227885783 | ||||||
chr2:227885947
|
C | T | 14 | a0001c0003t0002g0153a0001c0003t0002g0154a0001c0003t0002g0155others(11): Show | 14 | HG00438.hp2 HG02132.hp1 NA18940.hp1 others(11): Show |
intron_variant | MODIFIER | c.113+524C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227885947 | ||||||
chr2:227885975
|
C | CT | 22 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0062others(19): Show | 22 | HG01928.hp2 HG02027.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.113+568dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227885975 | |||||
chr2:227885975
|
C | CTT | 76 | a0001c0001t0001g0012a0001c0001t0001g0059a0001c0001t0001g0187others(73): Show | 77 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.113+567_113+568dup others(2): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227885975 | |||||
chr2:227885975
|
C | CTTT | 47 | a0001c0001t0001g0013a0001c0001t0001g0186a0001c0001t0001g0188others(44): Show | 47 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.113+566_113+568dup others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227885975 | |||||
chr2:227885975
|
CTTTTTTT | C | 21 | a0001c0003t0001g0152a0001c0003t0002g0153a0001c0003t0002g0154others(18): Show | 21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.113+562_113+568del others(7): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227885975 | |||||
chr2:227886010
|
T | C | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.113+587T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886010 | ||||||
chr2:227886036
|
T | C | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(160): Show | 164 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.113+613T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886036 | ||||||
chr2:227886043
|
C | T | 1 | a0001c0001t0001g0009 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.113+620C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886043 | ||||||
chr2:227886069
|
A | C | 37 | a0001c0001t0001g0030a0001c0001t0001g0176a0001c0001t0001g0179others(34): Show | 40 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.113+646A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886069 | ||||||
chr2:227886093
|
A | C | 34 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0014others(31): Show | 37 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.113+670A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886093 | ||||||
chr2:227886344
|
T | C | 257 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(254): Show | 265 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.113+921T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886344 | ||||||
chr2:227886462
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.113+1039C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886462 | ||||||
chr2:227886576
|
T | C | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(160): Show | 164 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.113+1153T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886576 | ||||||
chr2:227886636
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0067 | 3 | HG02257.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.113+1213T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886636 | ||||||
chr2:227886713
|
G | A | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(160): Show | 164 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.113+1290G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886713 | ||||||
chr2:227886750
|
C | T | 11 | a0003c0004t0001g0308a0003c0004t0001g0309a0003c0004t0001g0310others(8): Show | 11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.113+1327C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886750 | ||||||
chr2:227886788
|
TAAAC | T | 38 | a0001c0001t0001g0176a0001c0001t0001g0179a0002c0002t0001g0003others(35): Show | 41 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+1387_113+1390d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227886788 | |||||
chr2:227886916
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.113+1493A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886916 | ||||||
chr2:227886952
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0276 | 2 | HG01106.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.113+1529C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886952 | ||||||
chr2:227887090
|
C | G | 1 | a0003c0004t0001g0310 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113+1667C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887090 | ||||||
chr2:227887099
|
G | T | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0045others(47): Show | 52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.113+1676G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887099 | ||||||
chr2:227887157
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0143others(1): Show | 5 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+1734C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887157 | ||||||
chr2:227887158
|
G | A | 202 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0030others(199): Show | 206 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.113+1735G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887158 | ||||||
chr2:227887186
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.113+1763T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887186 | ||||||
chr2:227887321
|
T | C | 11 | a0003c0004t0001g0308a0003c0004t0001g0309a0003c0004t0001g0310others(8): Show | 11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.113+1898T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887321 | ||||||
chr2:227887411
|
C | T | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.113+1988C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887411 | ||||||
chr2:227887415
|
T | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(262): Show | 274 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.113+1992T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887415 | ||||||
chr2:227887433
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113+2010G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887433 | ||||||
chr2:227887443
|
A | G | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.113+2020A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887443 | ||||||
chr2:227887524
|
T | C | 117 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(114): Show | 118 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.113+2101T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887524 | ||||||
chr2:227887632
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 5 | HG00423.hp2 NA18962.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+2209G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887632 | ||||||
chr2:227887702
|
A | G | 11 | a0003c0004t0001g0308a0003c0004t0001g0309a0003c0004t0001g0310others(8): Show | 11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.114-2154A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887702 | ||||||
chr2:227887740
|
T | A | 3 | a0001c0003t0001g0297a0001c0003t0001g0306a0001c0003t0001g0307 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.114-2116T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887740 | ||||||
chr2:227887988
|
G | T | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(160): Show | 164 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.114-1868G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887988 | ||||||
chr2:227888089
|
T | C | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(160): Show | 164 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.114-1767T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888089 | ||||||
chr2:227888317
|
T | G | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(160): Show | 164 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.114-1539T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888317 | ||||||
chr2:227888408
|
C | A | 1 | a0001c0001t0001g0008 | 2 | NA18994.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.114-1448C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888408 | ||||||
chr2:227888440
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.114-1416C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888440 | ||||||
chr2:227888521
|
G | A | 1 | a0003c0004t0001g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.114-1335G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888521 | ||||||
chr2:227888558
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.114-1298G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888558 | ||||||
chr2:227888727
|
A | G | 1 | a0001c0003t0002g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.114-1129A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888727 | ||||||
chr2:227888736
|
G | A | 257 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(254): Show | 265 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.114-1120G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888736 | ||||||
chr2:227888751
|
T | C | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.114-1105T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888751 | ||||||
chr2:227888793
|
C | T | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.114-1063C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888793 | ||||||
chr2:227888794
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0277 | 3 | HG02165.hp1 NA18947.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.114-1062G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888794 | ||||||
chr2:227888894
|
C | A | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.114-962C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888894 | ||||||
chr2:227889055
|
T | C | 21 | a0001c0003t0001g0152a0001c0003t0002g0153a0001c0003t0002g0154others(18): Show | 21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.114-801T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889055 | ||||||
chr2:227889234
|
A | G | 1 | a0001c0003t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.114-622A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889234 | ||||||
chr2:227889236
|
A | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0296 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.114-620A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889236 | ||||||
chr2:227889256
|
G | A | 37 | a0001c0001t0001g0030a0001c0001t0001g0176a0001c0001t0001g0179others(34): Show | 40 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.114-600G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889256 | ||||||
chr2:227889272
|
G | A | 131 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(128): Show | 132 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.114-584G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889272 | ||||||
chr2:227889319
|
A | G | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(160): Show | 164 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.114-537A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889319 | ||||||
chr2:227889336
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.114-520C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889336 | ||||||
chr2:227889340
|
G | A | 117 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(114): Show | 118 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.114-516G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889340 | ||||||
chr2:227889433
|
G | A | 12 | a0003c0004t0001g0305a0003c0004t0001g0308a0003c0004t0001g0309others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-423G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889433 | ||||||
chr2:227889515
|
G | A | 1 | a0001c0001t0001g0262 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.114-341G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889515 | ||||||
chr2:227889549
|
G | A | 3 | a0001c0003t0001g0297a0001c0003t0001g0306a0001c0003t0001g0307 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.114-307G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889549 | ||||||
chr2:227889567
|
A | G | 21 | a0001c0003t0001g0152a0001c0003t0002g0153a0001c0003t0002g0154others(18): Show | 21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.114-289A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889567 | ||||||
chr2:227889584
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-272T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889584 | ||||||
chr2:227889591
|
T | A | 12 | a0003c0004t0001g0305a0003c0004t0001g0308a0003c0004t0001g0309others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-265T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889591 | ||||||
chr2:227889633
|
A | G | 46 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(43): Show | 46 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.114-223A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889633 | ||||||
chr2:227889688
|
G | T | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.114-168G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889688 | ||||||
chr2:227889699
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.114-157C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889699 | ||||||
chr2:227889846
|
T | A | 1 | a0001c0001t0001g0278 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.114-10T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889846 | ||||||
chr2:227890151
|
A | G | 34 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0014others(31): Show | 37 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.258+151A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890151 | ||||||
chr2:227890292
|
CT | C | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.258+299delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 227890292 | |||||
chr2:227890349
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | NA18957.hp1 NA18962.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.258+349C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890349 | ||||||
chr2:227890350
|
G | A | 32 | a0001c0003t0001g0152a0001c0003t0001g0297a0001c0003t0001g0298others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.258+350G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890350 | ||||||
chr2:227890383
|
T | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+383T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890383 | ||||||
chr2:227890402
|
G | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+402G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890402 | ||||||
chr2:227890404
|
A | G | 11 | a0003c0004t0001g0308a0003c0004t0001g0309a0003c0004t0001g0310others(8): Show | 11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.258+404A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890404 | ||||||
chr2:227890480
|
C | T | 2 | a0001c0003t0002g0174a0001c0003t0002g0175 | 2 | NA18956.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.258+480C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890480 | ||||||
chr2:227890557
|
C | G | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.258+557C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890557 | ||||||
chr2:227890578
|
T | G | 4 | a0001c0001t0001g0191a0001c0001t0001g0225a0001c0001t0001g0231others(1): Show | 4 | NA18961.hp2 NA19000.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+578T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890578 | ||||||
chr2:227890584
|
A | G | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.258+584A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890584 | ||||||
chr2:227890635
|
A | G | 47 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(44): Show | 47 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.259-620A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890635 | ||||||
chr2:227890639
|
G | A | 1 | a0001c0003t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.259-616G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890639 | ||||||
chr2:227890639
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.259-616G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890639 | ||||||
chr2:227890728
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.259-527G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890728 | ||||||
chr2:227890764
|
T | A | 34 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0014others(31): Show | 37 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.259-491T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890764 | ||||||
chr2:227890870
|
C | T | 32 | a0001c0003t0001g0152a0001c0003t0001g0297a0001c0003t0001g0298others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.259-385C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890870 | ||||||
chr2:227890871
|
A | G | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.259-384A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890871 | ||||||
chr2:227890872
|
T | G | 32 | a0001c0003t0001g0152a0001c0003t0001g0297a0001c0003t0001g0298others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.259-383T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890872 | ||||||
chr2:227891031
|
C | G | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.259-224C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227891031 | ||||||
chr2:227891428
|
T | C | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.317+115T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891428 | ||||||
chr2:227891573
|
G | A | 32 | a0001c0003t0001g0152a0001c0003t0001g0297a0001c0003t0001g0298others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.317+260G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891573 | ||||||
chr2:227891693
|
G | A | 34 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0014others(31): Show | 37 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.317+380G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891693 | ||||||
chr2:227891784
|
A | G | 1 | a0006c0010t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.317+471A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891784 | ||||||
chr2:227891790
|
A | G | 32 | a0001c0003t0001g0152a0001c0003t0001g0297a0001c0003t0001g0298others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.317+477A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891790 | ||||||
chr2:227891820
|
A | G | 5 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0023others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+507A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891820 | ||||||
chr2:227891841
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0067 | 3 | HG02257.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.317+528A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891841 | ||||||
chr2:227891897
|
G | T | 32 | a0001c0003t0001g0152a0001c0003t0001g0297a0001c0003t0001g0298others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.317+584G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891897 | ||||||
chr2:227891965
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.317+652G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891965 | ||||||
chr2:227892059
|
C | T | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.317+746C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892059 | ||||||
chr2:227892137
|
A | ATTTT | 47 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(44): Show | 47 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.317+833_317+836dup others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 227892137 | |||||
chr2:227892198
|
T | A | 1 | a0001c0001t0001g0038 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.317+885T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892198 | ||||||
chr2:227892404
|
G | T | 2 | a0001c0001t0001g0062a0008c0008t0001g0323 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.317+1091G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892404 | ||||||
chr2:227892446
|
T | C | 1 | a0003c0004t0001g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.317+1133T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892446 | ||||||
chr2:227892460
|
T | C | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.317+1147T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892460 | ||||||
chr2:227892517
|
C | G | 16 | a0001c0001t0001g0062a0003c0004t0001g0305a0003c0004t0001g0308others(13): Show | 16 | HG00438.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.317+1204C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892517 | ||||||
chr2:227892604
|
G | A | 165 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(162): Show | 166 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.318-1191G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892604 | ||||||
chr2:227892617
|
A | G | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-1178A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892617 | ||||||
chr2:227892618
|
G | A | 2 | a0003c0004t0001g0319a0003c0004t0001g0320 | 2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.318-1177G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892618 | ||||||
chr2:227892709
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.318-1086G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892709 | ||||||
chr2:227892774
|
T | C | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318-1021T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892774 | ||||||
chr2:227893004
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.318-791G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893004 | ||||||
chr2:227893094
|
C | CCCGT | 16 | a0001c0001t0001g0062a0003c0004t0001g0305a0003c0004t0001g0308others(13): Show | 16 | HG00438.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.318-699_318-698ins others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 227893094 | |||||
chr2:227893097
|
A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(263): Show | 275 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.318-698A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893097 | ||||||
chr2:227893140
|
C | T | 2 | a0001c0001t0001g0062a0008c0008t0001g0323 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.318-655C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893140 | ||||||
chr2:227893143
|
A | G | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-652A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893143 | ||||||
chr2:227893185
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0277 | 3 | HG02165.hp1 NA18947.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.318-610G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893185 | ||||||
chr2:227893186
|
C | A | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-609C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893186 | ||||||
chr2:227893187
|
T | C | 2 | a0001c0003t0001g0300a0005c0011t0001g0299 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.318-608T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893187 | ||||||
chr2:227893211
|
A | C | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318-584A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893211 | ||||||
chr2:227893357
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.318-438A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893357 | ||||||
chr2:227893367
|
T | A | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-428T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893367 | ||||||
chr2:227893391
|
C | T | 48 | a0001c0001t0001g0062a0001c0003t0001g0152a0001c0003t0001g0297others(45): Show | 48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-404C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893391 | ||||||
chr2:227893447
|
C | T | 16 | a0001c0001t0001g0062a0003c0004t0001g0305a0003c0004t0001g0308others(13): Show | 16 | HG00438.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.318-348C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893447 | ||||||
chr2:227893473
|
C | T | 1 | a0003c0004t0001g0312 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.318-322C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893473 | ||||||
chr2:227893533
|
G | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0045others(47): Show | 52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.318-262G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893533 | ||||||
chr2:227893651
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.318-144G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893651 | ||||||
chr2:227893662
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA18957.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.318-133A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893662 | ||||||
chr2:227893671
|
T | TAAAC | 46 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(43): Show | 51 | HG00099.hp2 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.318-102_318-99dupA others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 227893671 | |||||
chr2:227893683
|
C | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0012t0001g0070 | 3 | HG01109.hp1 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.318-112C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893683 | ||||||
chr2:227893740
|
C | A | 116 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(113): Show | 117 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.318-55C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893740 | ||||||
chr2:227893919
|
T | G | 1 | a0001c0001t0001g0279 | 1 | NA18988.hp2 | splice_donor_variant&intron_variant | HIGH | c.440+2T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227893919 | ||||||
chr2:227894002
|
G | A | 11 | a0003c0004t0001g0308a0003c0004t0001g0309a0003c0004t0001g0310others(8): Show | 11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.440+85G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894002 | ||||||
chr2:227894094
|
A | C | 1 | a0001c0001t0001g0261 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.440+177A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894094 | ||||||
chr2:227894128
|
G | T | 1 | a0001c0003t0001g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.440+211G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894128 | ||||||
chr2:227894167
|
C | T | 1 | a0001c0003t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.440+250C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894167 | ||||||
chr2:227894216
|
C | T | 1 | a0002c0002t0001g0025 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.440+299C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894216 | ||||||
chr2:227894285
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.440+368G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894285 | ||||||
chr2:227894314
|
G | T | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+397G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894314 | ||||||
chr2:227894461
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0266 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.440+544C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894461 | ||||||
chr2:227894500
|
G | T | 1 | a0001c0001t0001g0045 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.440+583G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894500 | ||||||
chr2:227894553
|
C | T | 32 | a0001c0003t0001g0152a0001c0003t0001g0297a0001c0003t0001g0298others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.440+636C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894553 | ||||||
chr2:227894700
|
T | A | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+783T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894700 | ||||||
chr2:227894712
|
C | A | 2 | a0002c0002t0001g0015a0002c0002t0001g0016 | 2 | HG01358.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.440+795C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894712 | ||||||
chr2:227894761
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.440+844T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894761 | ||||||
chr2:227894801
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.440+884G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894801 | ||||||
chr2:227894815
|
C | T | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.440+898C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894815 | ||||||
chr2:227894830
|
C | A | 32 | a0001c0003t0001g0152a0001c0003t0001g0297a0001c0003t0001g0298others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.440+913C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894830 | ||||||
chr2:227894838
|
T | C | 220 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(217): Show | 225 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.440+921T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894838 | ||||||
chr2:227894938
|
A | G | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.440+1021A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894938 | ||||||
chr2:227895018
|
G | A | 1 | a0001c0003t0002g0174 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.440+1101G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895018 | ||||||
chr2:227895137
|
G | A | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+1220G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895137 | ||||||
chr2:227895299
|
A | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(68): Show | 75 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.440+1382A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895299 | ||||||
chr2:227895350
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.440+1433G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895350 | ||||||
chr2:227895587
|
T | C | 1 | a0002c0002t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.440+1670T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895587 | ||||||
chr2:227895620
|
C | T | 33 | a0001c0001t0001g0198a0001c0003t0001g0152a0001c0003t0001g0297others(30): Show | 33 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.440+1703C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895620 | ||||||
chr2:227895695
|
A | T | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.440+1778A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895695 | ||||||
chr2:227895827
|
A | G | 118 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(115): Show | 119 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.440+1910A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895827 | ||||||
chr2:227895905
|
A | C | 1 | a0001c0001t0001g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440+1988A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895905 | ||||||
chr2:227895922
|
A | G | 1 | a0003c0004t0001g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.440+2005A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895922 | ||||||
chr2:227896027
|
G | T | 1 | a0002c0002t0001g0157 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.440+2110G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896027 | ||||||
chr2:227896198
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.441-1984A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896198 | ||||||
chr2:227896320
|
T | C | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.441-1862T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896320 | ||||||
chr2:227896487
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG00673.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.441-1695C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896487 | ||||||
chr2:227896559
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.441-1623A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896559 | ||||||
chr2:227896577
|
C | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0197a0001c0001t0001g0203others(21): Show | 25 | HG00323.hp1 HG00735.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.441-1605C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896577 | ||||||
chr2:227896593
|
A | AGT | 24 | a0001c0001t0001g0179a0001c0001t0001g0186a0001c0001t0001g0256others(21): Show | 24 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.441-1552_441-1551d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
A | AGTGT | 17 | a0001c0001t0001g0030a0001c0001t0001g0073a0001c0001t0001g0202others(14): Show | 18 | HG01074.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.441-1554_441-1551d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
A | AGTGTGT | 11 | a0001c0003t0002g0169a0001c0003t0002g0175a0001c0003t0002g0181others(8): Show | 13 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.441-1556_441-1551d others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
A | AGTGTGTG others(1): Show |
16 | a0001c0003t0002g0153a0001c0003t0002g0154a0001c0003t0002g0155others(13): Show | 16 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.441-1558_441-1551d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
A | AGTGTGTG others(3): Show |
2 | a0001c0003t0002g0178a0002c0002t0001g0148 | 2 | HG01433.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.441-1560_441-1551d others(12): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
A | AGTGTGTG others(7): Show |
1 | a0001c0003t0002g0173 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.441-1564_441-1551d others(16): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
AGT | A | 120 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0012others(117): Show | 123 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.441-1552_441-1551d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
AGTGT | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(45): Show | 53 | HG00099.hp2 HG00673.hp1 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.441-1554_441-1551d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
AGTGTGT | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 60 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.441-1556_441-1551d others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
AGTGTGTG others(1): Show |
A | 10 | a0001c0001t0001g0065a0001c0001t0001g0078a0001c0001t0001g0079others(7): Show | 10 | HG02165.hp2 HG02809.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.441-1558_441-1551d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
AGTGTGTG others(5): Show |
A | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.441-1562_441-1551d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.441-1564_441-1551d others(16): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896593
|
AGTGTGTG others(11): Show |
A | 1 | a0002c0002t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.441-1568_441-1551d others(20): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | |||||
chr2:227896665
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0179 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.441-1517C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896665 | ||||||
chr2:227896709
|
C | T | 1 | a0001c0003t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.441-1473C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896709 | ||||||
chr2:227896742
|
A | C | 1 | a0001c0001t0001g0274 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.441-1440A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896742 | ||||||
chr2:227896766
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.441-1416T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896766 | ||||||
chr2:227896947
|
A | G | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.441-1235A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896947 | ||||||
chr2:227897040
|
C | T | 1 | a0003c0004t0001g0317 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.441-1142C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897040 | ||||||
chr2:227897054
|
C | G | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.441-1128C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897054 | ||||||
chr2:227897093
|
G | GA | 9 | a0001c0001t0001g0064a0001c0001t0001g0083a0001c0001t0001g0084others(6): Show | 9 | HG01975.hp1 HG02027.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.441-1071dupA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227897093 | |||||
chr2:227897093
|
GA | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(88): Show | 95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.441-1071delA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227897093 | |||||
chr2:227897100
|
A | G | 10 | a0003c0004t0001g0308a0003c0004t0001g0309a0003c0004t0001g0310others(7): Show | 10 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.441-1082A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897100 | ||||||
chr2:227897298
|
A | G | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-884A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897298 | ||||||
chr2:227897358
|
C | T | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-824C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897358 | ||||||
chr2:227897401
|
G | T | 22 | a0001c0003t0001g0316a0001c0003t0002g0153a0001c0003t0002g0154others(19): Show | 22 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.441-781G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897401 | ||||||
chr2:227897484
|
T | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0119 | 2 | NA18984.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.441-698T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897484 | ||||||
chr2:227897612
|
C | G | 1 | a0001c0001t0001g0109 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.441-570C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897612 | ||||||
chr2:227897614
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 91 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.441-568C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897614 | ||||||
chr2:227897748
|
T | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 91 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.441-434T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897748 | ||||||
chr2:227897891
|
A | G | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-291A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897891 | ||||||
chr2:227897951
|
CCAAA | C | 32 | a0001c0003t0001g0297a0001c0003t0001g0298a0001c0003t0001g0300others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.441-226_441-223del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227897951 | |||||
chr2:227898017
|
C | G | 1 | a0002c0002t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.441-165C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227898017 | ||||||
chr2:227898470
|
G | A | 117 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(114): Show | 118 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.540+189G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898470 | ||||||
chr2:227898603
|
A | G | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.540+322A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898603 | ||||||
chr2:227898628
|
A | T | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.540+347A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898628 | ||||||
chr2:227898827
|
G | T | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.540+546G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898827 | ||||||
chr2:227898850
|
T | G | 31 | a0001c0003t0001g0297a0001c0003t0001g0298a0001c0003t0001g0300others(28): Show | 31 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.540+569T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898850 | ||||||
chr2:227898953
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.540+672A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898953 | ||||||
chr2:227899119
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.540+838A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899119 | ||||||
chr2:227899178
|
A | G | 117 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(114): Show | 118 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.540+897A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899178 | ||||||
chr2:227899187
|
C | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(217): Show | 225 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.540+906C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899187 | ||||||
chr2:227899188
|
T | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(217): Show | 225 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.540+907T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899188 | ||||||
chr2:227899214
|
A | C | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.540+933A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899214 | ||||||
chr2:227899238
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.540+957C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899238 | ||||||
chr2:227899503
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(250): Show | 261 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.540+1222T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899503 | ||||||
chr2:227899648
|
A | G | 1 | a0001c0003t0002g0178 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.540+1367A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899648 | ||||||
chr2:227899792
|
C | A | 22 | a0001c0001t0001g0012a0001c0001t0001g0197a0001c0001t0001g0205others(19): Show | 23 | HG00323.hp1 HG00735.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.540+1511C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899792 | ||||||
chr2:227899957
|
T | C | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.540+1676T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899957 | ||||||
chr2:227900122
|
A | G | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+1841A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900122 | ||||||
chr2:227900253
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0256 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.540+1972G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900253 | ||||||
chr2:227900349
|
A | G | 6 | a0001c0001t0001g0197a0001c0001t0001g0289a0001c0001t0001g0290others(3): Show | 6 | HG00323.hp1 HG00735.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+2068A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900349 | ||||||
chr2:227900456
|
C | T | 3 | a0001c0001t0001g0247a0001c0001t0001g0252a0001c0001t0001g0284 | 3 | HG02735.hp1 HG02738.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.540+2175C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900456 | ||||||
chr2:227900531
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+2250G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900531 | ||||||
chr2:227900558
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG01099.hp1 HG01109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.540+2277C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900558 | ||||||
chr2:227900674
|
G | A | 7 | a0001c0001t0001g0038a0001c0003t0001g0298a0001c0003t0001g0300others(4): Show | 7 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-2328G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900674 | ||||||
chr2:227900875
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.541-2127G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900875 | ||||||
chr2:227901016
|
A | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 325 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.541-1986A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901016 | ||||||
chr2:227901037
|
C | T | 1 | a0001c0003t0002g0156 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.541-1965C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901037 | ||||||
chr2:227901040
|
T | G | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.541-1962T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901040 | ||||||
chr2:227901138
|
C | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 263 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.541-1864C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901138 | ||||||
chr2:227901178
|
A | G | 1 | a0001c0003t0001g0303 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.541-1824A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901178 | ||||||
chr2:227901179
|
G | T | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.541-1823G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901179 | ||||||
chr2:227901328
|
AC | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0068others(4): Show | 8 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-1673delC | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901328 | ||||||
chr2:227901411
|
G | T | 1 | a0002c0002t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.541-1591G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901411 | ||||||
chr2:227901491
|
A | G | 123 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(120): Show | 124 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.541-1511A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901491 | ||||||
chr2:227901493
|
T | G | 129 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(126): Show | 130 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.541-1509T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901493 | ||||||
chr2:227901721
|
C | A | 26 | a0001c0001t0001g0062a0001c0001t0001g0198a0001c0003t0001g0297others(23): Show | 26 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.541-1281C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901721 | ||||||
chr2:227901809
|
T | C | 1 | a0001c0003t0002g0173 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.541-1193T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901809 | ||||||
chr2:227901861
|
G | A | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.541-1141G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901861 | ||||||
chr2:227901917
|
G | A | 2 | a0001c0001t0001g0198a0001c0003t0001g0297 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.541-1085G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901917 | ||||||
chr2:227901938
|
C | T | 20 | a0001c0001t0001g0073a0001c0003t0001g0298a0001c0003t0001g0300others(17): Show | 20 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.541-1064C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901938 | ||||||
chr2:227902244
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.541-758G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902244 | ||||||
chr2:227902354
|
C | T | 1 | a0001c0003t0002g0155 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.541-648C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902354 | ||||||
chr2:227902357
|
G | T | 1 | a0001c0003t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.541-645G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902357 | ||||||
chr2:227902438
|
T | C | 2 | a0001c0001t0001g0073a0003c0004t0001g0305 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.541-564T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902438 | ||||||
chr2:227902470
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.541-532A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902470 | ||||||
chr2:227902479
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.541-523G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902479 | ||||||
chr2:227902674
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | NA18979.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.541-328G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902674 | ||||||
chr2:227902703
|
C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 59 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.541-299C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902703 | ||||||
chr2:227902710
|
T | G | 1 | a0001c0001t0001g0293 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.541-292T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902710 | ||||||
chr2:227902902
|
T | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(308): Show | 325 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.541-100T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902902 | ||||||
chr2:227902915
|
G | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 127 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.541-87G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902915 | ||||||
chr2:227902992
|
TG | T | 1 | a0001c0001t0001g0002 | 3 | HG02622.hp2 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.541-9delG | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902992 | ||||||
chr2:227903361
|
T | C | 1 | a0002c0002t0001g0027 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.648+252T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903361 | ||||||
chr2:227903441
|
T | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 129 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.648+332T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903441 | ||||||
chr2:227903476
|
C | T | 2 | a0001c0001t0001g0198a0001c0003t0001g0297 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+367C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903476 | ||||||
chr2:227903638
|
T | TCTCCCCT others(10): Show |
7 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(4): Show | 7 | HG02723.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.648+582_648+598dup others(17): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 227903638 | |||||
chr2:227903638
|
TCTCCCCT others(10): Show |
T | 43 | a0001c0001t0001g0030a0001c0001t0001g0073a0001c0001t0001g0202others(40): Show | 46 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.648+582_648+598del others(17): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 227903638 | |||||
chr2:227903768
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(121): Show | 131 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.648+659A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903768 | ||||||
chr2:227903808
|
G | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(121): Show | 131 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.648+699G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903808 | ||||||
chr2:227903835
|
C | T | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0045others(47): Show | 52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.648+726C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903835 | ||||||
chr2:227903836
|
C | A | 1 | a0002c0002t0001g0157 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.648+727C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903836 | ||||||
chr2:227903943
|
C | T | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.648+834C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903943 | ||||||
chr2:227903988
|
G | GT | 122 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 129 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.648+889dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 227903988 | |||||
chr2:227904188
|
A | G | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.649-741A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227904188 | ||||||
chr2:227904277
|
T | C | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.649-652T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227904277 | ||||||
chr2:227904528
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.649-401T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227904528 | ||||||
chr2:227904718
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.649-211T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227904718 | ||||||
chr2:227905215
|
C | T | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.755+180C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905215 | ||||||
chr2:227905510
|
A | G | 2 | a0001c0001t0001g0198a0001c0003t0001g0297 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.755+475A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905510 | ||||||
chr2:227905583
|
C | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 130 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.755+548C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905583 | ||||||
chr2:227905743
|
T | C | 1 | a0003c0004t0001g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.756-493T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905743 | ||||||
chr2:227905755
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.756-481T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905755 | ||||||
chr2:227905759
|
G | T | 10 | a0003c0004t0001g0308a0003c0004t0001g0309a0003c0004t0001g0310others(7): Show | 10 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.756-477G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905759 | ||||||
chr2:227905792
|
T | TTGCCC | 57 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 61 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.756-443_756-439dup others(5): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 227905792 | |||||
chr2:227905823
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 130 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.756-413C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905823 | ||||||
chr2:227905843
|
T | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 130 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.756-393T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905843 | ||||||
chr2:227905847
|
T | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(249): Show | 260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.756-389T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905847 | ||||||
chr2:227905848
|
G | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 129 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.756-388G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905848 | ||||||
chr2:227905869
|
T | C | 113 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(110): Show | 114 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.756-367T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905869 | ||||||
chr2:227905880
|
G | A | 113 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(110): Show | 114 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.756-356G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905880 | ||||||
chr2:227905882
|
T | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 263 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.756-354T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905882 | ||||||
chr2:227905894
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.756-342A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905894 | ||||||
chr2:227905904
|
A | G | 1 | a0003c0004t0001g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.756-332A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905904 | ||||||
chr2:227905915
|
T | C | 1 | a0003c0004t0001g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.756-321T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905915 | ||||||
chr2:227905918
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.756-318C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905918 | ||||||
chr2:227905956
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | NA18977.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.756-280G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905956 | ||||||
chr2:227906050
|
C | T | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.756-186C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227906050 | ||||||
chr2:227906231
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0231 | 2 | NA18961.hp2 NA19004.hp2 |
splice_region_variant&intron_variant | LOW | c.756-5T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227906231 | ||||||
chr2:227906413
|
A | T | 1 | a0001c0001t0001g0130 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.858+75A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906413 | ||||||
chr2:227906417
|
A | G | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.858+79A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906417 | ||||||
chr2:227906554
|
A | G | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.858+216A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906554 | ||||||
chr2:227906590
|
T | C | 1 | a0003c0004t0001g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.858+252T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906590 | ||||||
chr2:227906707
|
A | T | 38 | a0001c0001t0001g0030a0001c0001t0001g0202a0001c0001t0001g0229others(35): Show | 41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.858+369A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906707 | ||||||
chr2:227906847
|
C | G | 1 | a0001c0001t0001g0274 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.859-291C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906847 | ||||||
chr2:227907103
|
C | CT | 13 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(10): Show | 13 | HG00642.hp2 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.859-24dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 227907103 | |||||
chr2:227907115
|
G | T | 2 | a0001c0001t0001g0073a0003c0004t0001g0305 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.859-23G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227907115 | ||||||
chr2:227907119
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.859-19T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227907119 | ||||||
chr2:227907404
|
G | C | 1 | a0002c0002t0001g0003 | 3 | HG01069.hp1 HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.973+152G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227907404 | ||||||
chr2:227907452
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 142 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.973+200T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227907452 | ||||||
chr2:227908097
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.973+845T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908097 | ||||||
chr2:227908103
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.973+851G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908103 | ||||||
chr2:227908171
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.973+919G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908171 | ||||||
chr2:227908199
|
G | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(45): Show | 53 | HG00099.hp2 HG00621.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.973+947G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908199 | ||||||
chr2:227908245
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 142 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.973+993T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908245 | ||||||
chr2:227908363
|
C | G | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.973+1111C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908363 | ||||||
chr2:227908430
|
C | T | 10 | a0001c0001t0001g0197a0001c0001t0001g0259a0001c0001t0001g0260others(7): Show | 10 | HG00323.hp1 HG00735.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+1178C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908430 | ||||||
chr2:227908571
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 71 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.973+1319T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908571 | ||||||
chr2:227908581
|
A | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 71 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.973+1329A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908581 | ||||||
chr2:227908608
|
G | T | 9 | a0003c0004t0001g0308a0003c0004t0001g0310a0003c0004t0001g0311others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.973+1356G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908608 | ||||||
chr2:227908690
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.973+1438A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908690 | ||||||
chr2:227908716
|
A | G | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.973+1464A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908716 | ||||||
chr2:227908808
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.973+1556T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908808 | ||||||
chr2:227908821
|
T | C | 5 | a0001c0001t0001g0062a0001c0001t0001g0198a0001c0003t0001g0297others(2): Show | 5 | HG00438.hp1 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.973+1569T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908821 | ||||||
chr2:227908889
|
A | T | 1 | a0001c0001t0001g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.973+1637A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908889 | ||||||
chr2:227908912
|
C | T | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.973+1660C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908912 | ||||||
chr2:227909053
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 142 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.973+1801T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909053 | ||||||
chr2:227909232
|
T | TTATC | 118 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(115): Show | 124 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.973+2018_973+2021d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | |||||
chr2:227909232
|
T | TTATCTAT others(1): Show |
93 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(90): Show | 99 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.973+2014_973+2021d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | |||||
chr2:227909232
|
T | TTATCTAT others(5): Show |
53 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0047others(50): Show | 55 | HG00642.hp2 HG00673.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.973+2010_973+2021d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | |||||
chr2:227909232
|
T | TTATCTAT others(9): Show |
13 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0059others(10): Show | 13 | HG00099.hp1 HG00423.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.973+2006_973+2021d others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | |||||
chr2:227909232
|
TTATC | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0003t0001g0316others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.973+2018_973+2021d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | |||||
chr2:227909232
|
TTATCTAT others(1): Show |
T | 20 | a0001c0003t0002g0153a0001c0003t0002g0154a0001c0003t0002g0155others(17): Show | 20 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.973+2014_973+2021d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | |||||
chr2:227909258
|
A | ATCTGTCT others(9): Show |
1 | a0001c0003t0002g0314 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.973+2009_973+2010i others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909258 | |||||
chr2:227909262
|
A | G | 1 | a0001c0003t0002g0314 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.973+2010A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909262 | ||||||
chr2:227909266
|
A | G | 21 | a0001c0003t0002g0153a0001c0003t0002g0154a0001c0003t0002g0155others(18): Show | 21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.973+2014A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909266 | ||||||
chr2:227909270
|
A | ATCTG | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.973+2034_973+2037d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909270 | |||||
chr2:227909270
|
A | ATCTGTCT others(1): Show |
4 | a0001c0001t0001g0076a0001c0001t0001g0077a0002c0002t0001g0017others(1): Show | 4 | HG01515.hp1 HG01934.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.973+2030_973+2037d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909270 | |||||
chr2:227909270
|
A | ATCTGTCT others(9): Show |
1 | a0001c0003t0001g0316 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.973+2022_973+2037d others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909270 | |||||
chr2:227909270
|
A | G | 21 | a0001c0003t0002g0153a0001c0003t0002g0154a0001c0003t0002g0155others(18): Show | 21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.973+2018A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909270 | ||||||
chr2:227909270
|
ATCTG | A | 45 | a0001c0001t0001g0059a0001c0001t0001g0187a0001c0001t0001g0189others(42): Show | 45 | HG00423.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.973+2034_973+2037d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909270 | |||||
chr2:227909325
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0107 | 2 | NA18948.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.973+2073T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909325 | ||||||
chr2:227909414
|
A | T | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0078others(5): Show | 8 | HG02165.hp2 NA18941.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.973+2162A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909414 | ||||||
chr2:227909440
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.973+2188G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909440 | ||||||
chr2:227909449
|
T | TAC | 5 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0003t0001g0306others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.973+2207_973+2208d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909449 | |||||
chr2:227909461
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.973+2209T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909461 | ||||||
chr2:227909513
|
A | G | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.973+2261A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909513 | ||||||
chr2:227909533
|
T | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 142 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.973+2281T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909533 | ||||||
chr2:227909670
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.973+2418G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909670 | ||||||
chr2:227909727
|
G | A | 5 | a0001c0001t0001g0062a0001c0001t0001g0198a0001c0003t0001g0297others(2): Show | 5 | HG00438.hp1 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.973+2475G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909727 | ||||||
chr2:227909756
|
A | G | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.973+2504A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909756 | ||||||
chr2:227910086
|
T | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0142 | 4 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.973+2834T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910086 | ||||||
chr2:227910146
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(5): Show | 8 | HG01106.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.973+2894G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910146 | ||||||
chr2:227910165
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.973+2913A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910165 | ||||||
chr2:227910209
|
C | T | 1 | a0002c0002t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+2957C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910209 | ||||||
chr2:227910326
|
A | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.973+3074A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910326 | ||||||
chr2:227910334
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.973+3082G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910334 | ||||||
chr2:227910350
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.973+3098G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910350 | ||||||
chr2:227910427
|
A | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.973+3175A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910427 | ||||||
chr2:227910438
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.973+3186A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910438 | ||||||
chr2:227910465
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.973+3213C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910465 | ||||||
chr2:227910477
|
T | G | 22 | a0001c0003t0001g0316a0001c0003t0002g0153a0001c0003t0002g0154others(19): Show | 22 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.973+3225T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910477 | ||||||
chr2:227910495
|
A | AAC | 46 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0074others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.973+3272_973+3273d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910495
|
A | AACAC | 70 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0035others(67): Show | 71 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.973+3270_973+3273d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910495
|
A | AACACAC | 27 | a0001c0001t0001g0044a0001c0001t0001g0221a0001c0001t0001g0286others(24): Show | 27 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.973+3268_973+3273d others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910495
|
A | AACACACA others(1): Show |
33 | a0001c0001t0001g0046a0001c0001t0001g0198a0001c0001t0001g0202others(30): Show | 34 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.973+3266_973+3273d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910495
|
A | AACACACA others(3): Show |
7 | a0001c0001t0001g0002a0001c0001t0001g0142a0001c0001t0001g0188others(4): Show | 9 | HG01433.hp2 HG01884.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.973+3264_973+3273d others(12): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910495
|
A | AACACACA others(5): Show |
30 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0030others(27): Show | 32 | HG00621.hp2 HG00735.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.973+3262_973+3273d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910495
|
A | AACACACA others(7): Show |
11 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0056others(8): Show | 13 | HG00558.hp2 HG01069.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.973+3260_973+3273d others(16): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910495
|
A | AACACACA others(9): Show |
14 | a0001c0001t0001g0111a0001c0001t0001g0122a0001c0001t0001g0123others(11): Show | 14 | HG00735.hp1 HG01175.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.973+3258_973+3273d others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910495
|
A | AACACACA others(11): Show |
7 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0001g0289others(4): Show | 7 | HG00323.hp1 HG01257.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.973+3256_973+3273d others(20): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910495
|
A | AACACACA others(13): Show |
1 | a0001c0001t0001g0115 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.973+3254_973+3273d others(22): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910495
|
AAC | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0043others(4): Show | 10 | HG00673.hp1 NA18949.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.973+3272_973+3273d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | |||||
chr2:227910525
|
C | CACACACA others(10): Show |
1 | a0001c0001t0001g0132 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.973+3273_973+3274i others(19): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910525 | ||||||
chr2:227910529
|
T | C | 1 | a0002c0002t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+3277T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910529 | ||||||
chr2:227910661
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.973+3409C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910661 | ||||||
chr2:227910698
|
C | T | 2 | a0001c0001t0001g0073a0003c0004t0001g0305 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.973+3446C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910698 | ||||||
chr2:227910730
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.973+3478T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910730 | ||||||
chr2:227910802
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.973+3550A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910802 | ||||||
chr2:227911004
|
C | T | 67 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 71 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.973+3752C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911004 | ||||||
chr2:227911005
|
A | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(250): Show | 261 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.973+3753A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911005 | ||||||
chr2:227911084
|
C | A | 36 | a0001c0001t0001g0202a0001c0001t0001g0229a0001c0001t0001g0251others(33): Show | 39 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.973+3832C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911084 | ||||||
chr2:227911197
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.973+3945T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911197 | ||||||
chr2:227911225
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.973+3973T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911225 | ||||||
chr2:227911227
|
T | TGTGTATA others(43): Show |
2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.973+4014_973+4015i others(52): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911227 | |||||
chr2:227911231
|
TATATATA others(1): Show |
T | 3 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0067 | 4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.973+3997_973+4004d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911231 | |||||
chr2:227911239
|
C | CATATACA others(5): Show |
1 | a0002c0002t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+3992_973+3993i others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | |||||
chr2:227911239
|
C | CATATATA others(27): Show |
7 | a0001c0001t0001g0061a0001c0003t0001g0298a0001c0003t0001g0300others(4): Show | 7 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.973+3996_973+3997i others(36): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | |||||
chr2:227911239
|
C | CATATATA others(35): Show |
83 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0045others(80): Show | 88 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.973+4014_973+4015i others(44): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | |||||
chr2:227911239
|
C | CATATATA others(55): Show |
1 | a0001c0001t0001g0138 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.973+4014_973+4015i others(64): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | |||||
chr2:227911239
|
C | CATATATA others(57): Show |
7 | a0001c0001t0001g0197a0001c0001t0001g0289a0001c0001t0001g0290others(4): Show | 7 | HG00323.hp1 HG00735.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.973+4014_973+4015i others(66): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | |||||
chr2:227911239
|
C | CATATATA others(77): Show |
4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG00558.hp2 HG01496.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.973+4014_973+4015i others(86): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | |||||
chr2:227911239
|
C | CATATATA others(99): Show |
1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.973+4014_973+4015i others(108): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | |||||
chr2:227911239
|
C | CATATATA others(37): Show |
1 | a0003c0004t0001g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.973+4014_973+4015i others(46): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | |||||
chr2:227911247
|
C | CATATATA others(41): Show |
1 | a0001c0001t0001g0073 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.973+4014_973+4015i others(50): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911247 | |||||
chr2:227911249
|
T | TATATACA others(13): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0076 | 2 | HG02257.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.973+4014_973+4015i others(22): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911249 | |||||
chr2:227911249
|
TATATACA others(13): Show |
T | 1 | a0001c0001t0001g0086 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.973+4015_973+4034d others(22): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911249 | |||||
chr2:227911258
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0068others(4): Show | 8 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.973+4006G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911258 | ||||||
chr2:227911260
|
G | GTATATAT others(57): Show |
1 | a0002c0002t0001g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.973+4014_973+4015i others(66): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911260 | |||||
chr2:227911266
|
A | G | 102 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(99): Show | 103 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(100): Show |
intron_variant | MODIFIER | c.973+4014A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911266 | ||||||
chr2:227911267
|
C | CATATACA others(33): Show |
1 | a0001c0001t0001g0265 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.973+4016_973+4017i others(42): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911267 | |||||
chr2:227911267
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(305): Show | 322 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.973+4015C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911267 | ||||||
chr2:227911269
|
C | CATATACA others(55): Show |
1 | a0001c0001t0001g0123 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.973+4042_973+4043i others(64): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911269 | |||||
chr2:227911269
|
C | T | 1 | a0002c0002t0001g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.973+4017C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911269 | ||||||
chr2:227911295
|
T | TACACGTG others(15): Show |
1 | a0001c0001t0001g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.973+4053_973+4054i others(24): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911295 | |||||
chr2:227911299
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.973+4047C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911299 | ||||||
chr2:227911330
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.973+4078A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911330 | ||||||
chr2:227911352
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0068others(4): Show | 8 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.973+4100A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911352 | ||||||
chr2:227911367
|
C | T | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.973+4115C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911367 | ||||||
chr2:227911407
|
T | C | 3 | a0002c0002t0001g0014a0002c0002t0001g0019a0002c0002t0001g0020 | 3 | HG00642.hp2 HG01167.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.973+4155T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911407 | ||||||
chr2:227911669
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.973+4417T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911669 | ||||||
chr2:227911807
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.973+4555G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911807 | ||||||
chr2:227911933
|
A | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0107 | 2 | NA18948.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.973+4681A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911933 | ||||||
chr2:227911955
|
T | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.973+4703T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911955 | ||||||
chr2:227912029
|
GACA | G | 3 | a0001c0003t0002g0164a0001c0003t0002g0168a0001c0003t0002g0181 | 3 | HG01243.hp2 HG02293.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.973+4782_973+4784d others(5): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227912029 | |||||
chr2:227912207
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.973+4955T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912207 | ||||||
chr2:227912222
|
A | G | 114 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(111): Show | 115 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(112): Show |
intron_variant | MODIFIER | c.973+4970A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912222 | ||||||
chr2:227912280
|
T | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.973+5028T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912280 | ||||||
chr2:227912354
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.973+5102G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912354 | ||||||
chr2:227912512
|
A | G | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.973+5260A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912512 | ||||||
chr2:227912732
|
C | T | 253 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(250): Show | 261 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.973+5480C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912732 | ||||||
chr2:227912825
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.973+5573T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912825 | ||||||
chr2:227912845
|
C | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0093 | 2 | HG01496.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.973+5593C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912845 | ||||||
chr2:227912925
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.973+5673G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912925 | ||||||
chr2:227912940
|
C | T | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.973+5688C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912940 | ||||||
chr2:227912957
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.973+5705A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912957 | ||||||
chr2:227913069
|
G | A | 20 | a0001c0001t0001g0202a0001c0001t0001g0229a0001c0001t0001g0251others(17): Show | 23 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.974-5711G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913069 | ||||||
chr2:227913083
|
G | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0045others(57): Show | 62 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.974-5697G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913083 | ||||||
chr2:227913086
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.974-5694T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913086 | ||||||
chr2:227913155
|
T | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.974-5625T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913155 | ||||||
chr2:227913265
|
C | T | 38 | a0001c0001t0001g0030a0001c0001t0001g0202a0001c0001t0001g0229others(35): Show | 41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.974-5515C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913265 | ||||||
chr2:227913450
|
A | C | 2 | a0001c0001t0001g0073a0003c0004t0001g0305 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.974-5330A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913450 | ||||||
chr2:227913565
|
G | A | 1 | a0003c0004t0001g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.974-5215G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913565 | ||||||
chr2:227913736
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.974-5044A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913736 | ||||||
chr2:227913737
|
C | G | 22 | a0001c0003t0001g0316a0001c0003t0002g0153a0001c0003t0002g0154others(19): Show | 22 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.974-5043C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913737 | ||||||
chr2:227913823
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 71 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.974-4957T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913823 | ||||||
chr2:227913848
|
C | T | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.974-4932C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913848 | ||||||
chr2:227913849
|
C | T | 60 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0045others(57): Show | 62 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.974-4931C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913849 | ||||||
chr2:227913871
|
A | ATATC | 7 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0130others(4): Show | 7 | HG00438.hp1 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.974-4899_974-4896d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | |||||
chr2:227913871
|
A | ATATCTAT others(1): Show |
62 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(59): Show | 67 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.974-4903_974-4896d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | |||||
chr2:227913871
|
A | ATATCTAT others(5): Show |
31 | a0001c0001t0001g0202a0001c0001t0001g0229a0001c0001t0001g0251others(28): Show | 33 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.974-4907_974-4896d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | |||||
chr2:227913871
|
A | ATATCTAT others(9): Show |
6 | a0001c0003t0001g0297a0002c0002t0001g0017a0002c0002t0001g0158others(3): Show | 6 | HG01515.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-4896_974-4895i others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | |||||
chr2:227913871
|
A | ATATCTAT others(13): Show |
1 | a0001c0001t0001g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.974-4896_974-4895i others(22): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | |||||
chr2:227913871
|
A | ATATCTAT others(17): Show |
1 | a0002c0002t0001g0021 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.974-4896_974-4895i others(26): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | |||||
chr2:227913871
|
ATATC | A | 4 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(1): Show | 4 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.974-4899_974-4896d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | |||||
chr2:227913881
|
A | ATCTATCT others(21): Show |
1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.974-4896_974-4895i others(30): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | |||||
chr2:227913881
|
A | ATCTATCT others(5): Show |
1 | a0001c0001t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.974-4896_974-4895i others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | |||||
chr2:227913881
|
A | ATCTATCT others(5): Show |
1 | a0001c0001t0001g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.974-4896_974-4895i others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | |||||
chr2:227913881
|
A | ATCTG | 3 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0081 | 4 | HG02257.hp2 HG02965.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-4863_974-4860d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | |||||
chr2:227913881
|
A | G | 1 | a0001c0003t0001g0302 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.974-4899A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913881 | ||||||
chr2:227913881
|
ATCTG | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0038others(86): Show | 90 | HG00438.hp2 HG00558.hp1 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.974-4863_974-4860d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | |||||
chr2:227913881
|
ATCTGTCT others(1): Show |
A | 3 | a0001c0001t0001g0193a0001c0001t0001g0268a0003c0004t0001g0305 | 3 | NA18957.hp1 NA19084.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.974-4867_974-4860d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | |||||
chr2:227913885
|
G | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0062others(52): Show | 60 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.974-4895G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913885 | ||||||
chr2:227913889
|
G | A | 58 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0001g0229others(55): Show | 61 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.974-4891G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913889 | ||||||
chr2:227913893
|
G | A | 26 | a0001c0001t0001g0198a0001c0003t0001g0297a0001c0003t0002g0153others(23): Show | 26 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.974-4887G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913893 | ||||||
chr2:227913897
|
G | A | 1 | a0002c0002t0001g0157 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.974-4883G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913897 | ||||||
chr2:227913913
|
G | A | 7 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(4): Show | 7 | HG01891.hp1 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.974-4867G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913913 | ||||||
chr2:227913917
|
G | A | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(140): Show | 144 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.974-4863G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913917 | ||||||
chr2:227913921
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.974-4859A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913921 | ||||||
chr2:227913924
|
TA | T | 8 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(5): Show | 8 | HG01891.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.974-4855delA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913924 | ||||||
chr2:227913928
|
T | A | 8 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(5): Show | 8 | HG01891.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.974-4852T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913928 | ||||||
chr2:227913928
|
T | TA | 110 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 117 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.974-4852_974-4851i others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913928 | ||||||
chr2:227913931
|
A | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 117 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.974-4849A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913931 | ||||||
chr2:227913988
|
ATC | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.974-4770_974-4769d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913988 | |||||
chr2:227914045
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.974-4735G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914045 | ||||||
chr2:227914053
|
A | C | 2 | a0001c0001t0001g0198a0001c0003t0001g0297 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-4727A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914053 | ||||||
chr2:227914139
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.974-4641G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914139 | ||||||
chr2:227914153
|
A | G | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | NA18942.hp2 NA18984.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.974-4627A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914153 | ||||||
chr2:227914321
|
A | G | 39 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0202others(36): Show | 42 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.974-4459A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914321 | ||||||
chr2:227914394
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.974-4386C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914394 | ||||||
chr2:227914474
|
C | T | 12 | a0001c0001t0001g0060a0001c0001t0001g0202a0001c0001t0001g0229others(9): Show | 13 | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.974-4306C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914474 | ||||||
chr2:227914503
|
T | C | 23 | a0001c0003t0001g0316a0001c0003t0002g0153a0001c0003t0002g0154others(20): Show | 23 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.974-4277T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914503 | ||||||
chr2:227914852
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.974-3928A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914852 | ||||||
chr2:227914920
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 263 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.974-3860G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914920 | ||||||
chr2:227915090
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.974-3690G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915090 | ||||||
chr2:227915134
|
T | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0068others(4): Show | 8 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.974-3646T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915134 | ||||||
chr2:227915143
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0093 | 2 | HG01496.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.974-3637A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915143 | ||||||
chr2:227915195
|
G | T | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.974-3585G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915195 | ||||||
chr2:227915212
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.974-3568A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915212 | ||||||
chr2:227915229
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.974-3551T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915229 | ||||||
chr2:227915242
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0119 | 2 | NA18984.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.974-3538A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915242 | ||||||
chr2:227915243
|
T | C | 39 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0202others(36): Show | 42 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.974-3537T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915243 | ||||||
chr2:227915355
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 263 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.974-3425G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915355 | ||||||
chr2:227915356
|
T | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0045others(57): Show | 62 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.974-3424T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915356 | ||||||
chr2:227915603
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.974-3177C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915603 | ||||||
chr2:227915626
|
G | C | 5 | a0001c0001t0001g0062a0001c0001t0001g0198a0001c0003t0001g0297others(2): Show | 5 | HG00438.hp1 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-3154G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915626 | ||||||
chr2:227915694
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.974-3086A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915694 | ||||||
chr2:227915712
|
A | C | 1 | a0001c0003t0001g0306 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.974-3068A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915712 | ||||||
chr2:227915721
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0131a0001c0001t0001g0138 | 3 | HG01258.hp1 HG01261.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.974-3059C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915721 | ||||||
chr2:227915842
|
C | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0198a0001c0003t0001g0297 | 3 | HG02257.hp1 HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-2938C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915842 | ||||||
chr2:227915892
|
T | C | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | NA18942.hp2 NA18988.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.974-2888T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915892 | ||||||
chr2:227916168
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.974-2612A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916168 | ||||||
chr2:227916414
|
C | T | 1 | a0003c0004t0001g0320 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.974-2366C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916414 | ||||||
chr2:227916418
|
G | A | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.974-2362G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916418 | ||||||
chr2:227916475
|
C | A | 112 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(109): Show | 113 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.974-2305C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916475 | ||||||
chr2:227916560
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.974-2220C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916560 | ||||||
chr2:227916574
|
T | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 263 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.974-2206T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916574 | ||||||
chr2:227916584
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.974-2196G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916584 | ||||||
chr2:227916715
|
T | C | 39 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0202others(36): Show | 42 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.974-2065T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916715 | ||||||
chr2:227916756
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.974-2024A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916756 | ||||||
chr2:227917047
|
A | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 117 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.974-1733A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917047 | ||||||
chr2:227917087
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.974-1693G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917087 | ||||||
chr2:227917112
|
G | GTATC | 7 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0233others(4): Show | 7 | HG01081.hp2 HG01106.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-1638_974-1635d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | |||||
chr2:227917112
|
G | GTATCTAT others(1): Show |
4 | a0001c0001t0001g0196a0001c0001t0001g0210a0001c0001t0001g0252others(1): Show | 4 | HG01975.hp1 HG03017.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-1642_974-1635d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | |||||
chr2:227917112
|
G | GTATCTAT others(5): Show |
2 | a0001c0001t0001g0187a0001c0001t0001g0195 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.974-1646_974-1635d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | |||||
chr2:227917112
|
GTATC | G | 6 | a0001c0001t0001g0201a0001c0001t0001g0211a0001c0001t0001g0218others(3): Show | 6 | HG02056.hp1 HG03669.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-1638_974-1635d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | |||||
chr2:227917112
|
GTATCTAT others(1): Show |
G | 12 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0069others(9): Show | 13 | HG00621.hp1 HG01109.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.974-1642_974-1635d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | |||||
chr2:227917112
|
GTATCTAT others(5): Show |
G | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(51): Show | 58 | HG00673.hp1 HG01346.hp1 HG01496.hp1 others(55): Show |
intron_variant | MODIFIER | c.974-1646_974-1635d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | |||||
chr2:227917112
|
GTATCTAT others(9): Show |
G | 3 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0097 | 4 | HG01257.hp1 HG01258.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-1650_974-1635d others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | |||||
chr2:227917126
|
A | ATCTG | 7 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0060others(4): Show | 7 | HG00639.hp1 HG00738.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-1651_974-1650i others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917126 | |||||
chr2:227917130
|
A | G | 131 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 138 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.974-1650A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917130 | ||||||
chr2:227917130
|
ATCTATCT others(9): Show |
A | 3 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0001g0088 | 3 | HG00099.hp2 HG02165.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.974-1646_974-1631d others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917130 | |||||
chr2:227917134
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(121): Show | 131 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.974-1646A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917134 | ||||||
chr2:227917134
|
ATCTATCT others(5): Show |
A | 4 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0003t0001g0306others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.974-1642_974-1631d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917134 | |||||
chr2:227917137
|
T | C | 1 | a0002c0002t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.974-1643T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917137 | ||||||
chr2:227917138
|
A | ATCTG | 7 | a0001c0001t0001g0190a0001c0001t0001g0199a0001c0001t0001g0223others(4): Show | 7 | HG00558.hp1 HG01167.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.974-1639_974-1638i others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917138 | |||||
chr2:227917138
|
A | G | 6 | a0001c0001t0001g0191a0001c0001t0001g0219a0001c0001t0001g0231others(3): Show | 6 | HG00673.hp2 HG01361.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-1642A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917138 | ||||||
chr2:227917138
|
ATCTATCT others(1): Show |
A | 14 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0001g0033others(11): Show | 15 | HG01106.hp2 HG01884.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.974-1638_974-1631d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917138 | |||||
chr2:227917142
|
A | ATCTATCT others(5): Show |
3 | a0001c0001t0001g0234a0001c0001t0001g0244a0001c0001t0001g0257 | 3 | HG03579.hp2 NA19065.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.974-1635_974-1634i others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | |||||
chr2:227917142
|
A | ATCTATCT others(9): Show |
1 | a0001c0001t0001g0274 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.974-1635_974-1634i others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | |||||
chr2:227917142
|
A | ATCTATCT others(1): Show |
5 | a0001c0001t0001g0247a0001c0001t0001g0271a0001c0001t0001g0275others(2): Show | 5 | HG01978.hp1 HG02027.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-1635_974-1634i others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | |||||
chr2:227917142
|
A | ATCTATCT others(5): Show |
5 | a0001c0001t0001g0186a0001c0001t0001g0194a0001c0001t0001g0272others(2): Show | 5 | HG01928.hp1 NA18947.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.974-1635_974-1634i others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | |||||
chr2:227917142
|
A | ATCTG | 13 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0217others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.974-1602_974-1599d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | |||||
chr2:227917142
|
A | ATCTGTCT others(1): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0193a0001c0001t0001g0245others(2): Show | 5 | HG02135.hp2 HG03942.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.974-1606_974-1599d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | |||||
chr2:227917142
|
A | G | 48 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0060others(45): Show | 48 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.974-1638A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917142 | ||||||
chr2:227917142
|
ATCTG | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0046others(36): Show | 41 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.974-1602_974-1599d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | |||||
chr2:227917142
|
ATCTGTCT others(1): Show |
A | 4 | a0001c0001t0001g0143a0001c0001t0001g0261a0001c0001t0001g0265others(1): Show | 4 | HG01243.hp1 HG01978.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-1606_974-1599d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | |||||
chr2:227917142
|
ATCTGTCT others(5): Show |
A | 2 | a0002c0002t0001g0160a0002c0002t0001g0163 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.974-1610_974-1599d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | |||||
chr2:227917146
|
G | A | 82 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(79): Show | 85 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.974-1634G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917146 | ||||||
chr2:227917150
|
G | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0044others(18): Show | 24 | HG00423.hp2 HG00438.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.974-1630G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917150 | ||||||
chr2:227917154
|
G | A | 3 | a0001c0001t0001g0241a0004c0005t0003g0321a0004c0005t0003g0322 | 3 | HG00438.hp1 HG01074.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.974-1626G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917154 | ||||||
chr2:227917188
|
G | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(129): Show | 139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-1592G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917188 | ||||||
chr2:227917266
|
CT | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 138 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.974-1501delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917266 | |||||
chr2:227917266
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0109 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.974-1512_974-1501d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917266 | |||||
chr2:227917272
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.974-1508T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917272 | ||||||
chr2:227917299
|
C | T | 112 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(109): Show | 113 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.974-1481C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917299 | ||||||
chr2:227917330
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.974-1450A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917330 | ||||||
chr2:227917346
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.974-1434C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917346 | ||||||
chr2:227917347
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.974-1433A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917347 | ||||||
chr2:227917389
|
T | C | 2 | a0001c0001t0001g0198a0001c0003t0001g0297 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-1391T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917389 | ||||||
chr2:227917434
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.974-1346G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917434 | ||||||
chr2:227917459
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.974-1321A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917459 | ||||||
chr2:227917487
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.974-1293C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917487 | ||||||
chr2:227917503
|
T | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(321): Show | 339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.974-1277T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917503 | ||||||
chr2:227917528
|
G | A | 2 | a0001c0001t0001g0198a0001c0003t0001g0297 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-1252G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917528 | ||||||
chr2:227917561
|
A | AT | 38 | a0001c0001t0001g0060a0001c0001t0001g0202a0001c0001t0001g0229others(35): Show | 41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.974-1212dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917561 | |||||
chr2:227917584
|
T | G | 39 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0202others(36): Show | 42 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.974-1196T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917584 | ||||||
chr2:227917586
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.974-1194C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917586 | ||||||
chr2:227917587
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.974-1193C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917587 | ||||||
chr2:227917590
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.974-1190T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917590 | ||||||
chr2:227917591
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.974-1189C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917591 | ||||||
chr2:227917595
|
A | T | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.974-1185A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917595 | ||||||
chr2:227917817
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.974-963C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917817 | ||||||
chr2:227917971
|
A | T | 2 | a0001c0001t0001g0198a0001c0003t0001g0297 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-809A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917971 | ||||||
chr2:227918017
|
A | G | 1 | a0004c0005t0003g0322 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.974-763A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918017 | ||||||
chr2:227918038
|
G | GT | 3 | a0001c0001t0001g0286a0001c0001t0001g0294a0001c0001t0001g0295 | 3 | NA18939.hp2 NA18967.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.974-737dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918038 | |||||
chr2:227918050
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0142a0002c0002t0001g0180 | 5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.974-730C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918050 | ||||||
chr2:227918122
|
C | CTGCATCC others(13): Show |
1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.974-657_974-656ins others(20): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918122 | |||||
chr2:227918142
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.974-638G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918142 | ||||||
chr2:227918142
|
G | GTCCATCC others(1): Show |
21 | a0001c0001t0001g0112a0001c0001t0001g0131a0001c0001t0001g0197others(18): Show | 21 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.974-615_974-608dup others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918142 | |||||
chr2:227918142
|
G | GTCCATCC others(5): Show |
21 | a0001c0001t0001g0009a0001c0001t0001g0126a0001c0003t0001g0297others(18): Show | 22 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.974-619_974-608dup others(12): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918142 | |||||
chr2:227918142
|
G | GTCCATCC others(9): Show |
75 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0044others(72): Show | 81 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.974-623_974-608dup others(16): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918142 | |||||
chr2:227918142
|
G | GTCCATCC others(13): Show |
5 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0135others(2): Show | 5 | HG03491.hp1 HG04204.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-627_974-608dup others(20): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918142 | |||||
chr2:227918142
|
G | GTCCATCC others(17): Show |
1 | a0002c0002t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.974-631_974-608dup others(24): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918142 | |||||
chr2:227918146
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0195 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.974-634A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918146 | ||||||
chr2:227918148
|
C | CCATCCAT others(24): Show |
3 | a0001c0003t0002g0164a0001c0003t0002g0166a0001c0003t0002g0172 | 3 | HG02293.hp1 NA18993.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.974-608_974-607ins others(31): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918148 | |||||
chr2:227918148
|
C | CCATCCAT others(28): Show |
4 | a0001c0001t0001g0198a0004c0005t0003g0321a0004c0005t0003g0322others(1): Show | 4 | HG00438.hp1 HG02723.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.974-608_974-607ins others(35): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918148 | |||||
chr2:227918171
|
T | TCATC | 41 | a0001c0001t0001g0187a0001c0001t0001g0191a0001c0001t0001g0192others(38): Show | 41 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.974-561_974-558dup others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918171 | |||||
chr2:227918171
|
T | TCATCCAT others(1): Show |
24 | a0001c0001t0001g0059a0001c0001t0001g0196a0001c0001t0001g0199others(21): Show | 24 | HG00423.hp1 HG00673.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.974-565_974-558dup others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918171 | |||||
chr2:227918171
|
TCATC | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 75 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.974-561_974-558del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918171 | |||||
chr2:227918171
|
TCATCCAT others(1): Show |
T | 5 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 6 | HG01257.hp1 HG01258.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-565_974-558del others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918171 | |||||
chr2:227918175
|
C | CCATCATC others(19): Show |
1 | a0001c0003t0002g0314 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.974-601_974-600ins others(26): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918175 | |||||
chr2:227918175
|
C | CCATCCAT others(12): Show |
19 | a0001c0003t0001g0297a0001c0003t0001g0316a0001c0003t0002g0153others(16): Show | 19 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.974-603_974-585dup others(19): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918175 | |||||
chr2:227918179
|
C | CCATCCAT others(8): Show |
4 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0130others(1): Show | 4 | HG02055.hp1 HG02257.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-599_974-585dup others(15): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918179 | |||||
chr2:227918183
|
C | CCATCCAT others(4): Show |
45 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0045others(42): Show | 48 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.974-595_974-585dup others(11): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918183 | |||||
chr2:227918187
|
C | CCATCCAT | 18 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0112others(15): Show | 18 | HG00735.hp2 HG00738.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.974-591_974-585dup others(7): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918187 | |||||
chr2:227918191
|
C | CCAT | 38 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0060others(35): Show | 42 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.974-587_974-585dup others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918191 | |||||
chr2:227918260
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.974-520C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918260 | ||||||
chr2:227918269
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.974-511C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918269 | ||||||
chr2:227918418
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.974-362G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918418 | ||||||
chr2:227918420
|
G | T | 3 | a0002c0002t0001g0014a0002c0002t0001g0019a0002c0002t0001g0020 | 3 | HG00642.hp2 HG01167.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.974-360G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918420 | ||||||
chr2:227918473
|
T | C | 1 | a0001c0001t0001g0295 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.974-307T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918473 | ||||||
chr2:227918510
|
A | G | 2 | a0001c0001t0001g0198a0001c0003t0001g0297 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-270A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918510 | ||||||
chr2:227918547
|
A | G | 38 | a0001c0001t0001g0013a0001c0001t0001g0186a0001c0001t0001g0188others(35): Show | 38 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.974-233A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918547 | ||||||
chr2:227918648
|
A | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(260): Show | 272 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.974-132A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918648 | ||||||
chr2:227918694
|
G | T | 22 | a0001c0003t0001g0316a0001c0003t0002g0153a0001c0003t0002g0154others(19): Show | 22 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.974-86G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918694 | ||||||
chr2:227918731
|
G | C | 20 | a0001c0003t0002g0153a0001c0003t0002g0154a0001c0003t0002g0155others(17): Show | 20 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.974-49G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918731 | ||||||
chr2:227918763
|
C | A | 61 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0045others(58): Show | 63 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.974-17C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918763 | ||||||
chr2:227919206
|
AAAG | A | 119 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0030others(116): Show | 124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1050+353_1050+355d others(5): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227919206 | |||||
chr2:227919207
|
AAG | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0061others(8): Show | 13 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1050+353_1050+354d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227919207 | |||||
chr2:227919209
|
GA | G | 101 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(98): Show | 102 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(99): Show |
intron_variant | MODIFIER | c.1050+368delA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227919209 | |||||
chr2:227919209
|
GAA | G | 17 | a0001c0001t0001g0099a0001c0001t0001g0224a0001c0001t0001g0255others(14): Show | 17 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.1050+367_1050+368d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227919209 | |||||
chr2:227919210
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0061others(8): Show | 13 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1050+354A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919210 | ||||||
chr2:227919211
|
A | G | 119 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0030others(116): Show | 124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1050+355A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919211 | ||||||
chr2:227919212
|
A | G | 3 | a0002c0002t0001g0024a0002c0002t0001g0162a0002c0002t0001g0184 | 3 | HG01243.hp1 HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1050+356A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919212 | ||||||
chr2:227919220
|
A | G | 2 | a0004c0005t0003g0321a0004c0005t0003g0322 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1050+364A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919220 | ||||||
chr2:227919224
|
A | AGCATGCT others(38): Show |
1 | a0001c0001t0001g0193 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1050+369_1050+413d others(47): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227919224 | |||||
chr2:227919575
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0067 | 3 | HG02257.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1050+719T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919575 | ||||||
chr2:227919785
|
A | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(250): Show | 261 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.1050+929A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919785 | ||||||
chr2:227919889
|
C | T | 22 | a0001c0003t0001g0316a0001c0003t0002g0153a0001c0003t0002g0154others(19): Show | 22 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1050+1033C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919889 | ||||||
chr2:227919990
|
G | A | 2 | a0001c0003t0001g0316a0001c0003t0002g0314 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1050+1134G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919990 | ||||||
chr2:227920141
|
A | C | 3 | a0003c0004t0001g0308a0003c0004t0001g0310a0003c0004t0001g0315 | 3 | HG02976.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1051-1258A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920141 | ||||||
chr2:227920192
|
T | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0276 | 2 | HG01106.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1051-1207T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920192 | ||||||
chr2:227920260
|
G | A | 23 | a0001c0003t0001g0316a0001c0003t0002g0153a0001c0003t0002g0154others(20): Show | 23 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1051-1139G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920260 | ||||||
chr2:227920291
|
A | G | 5 | a0001c0003t0002g0153a0001c0003t0002g0154a0001c0003t0002g0155others(2): Show | 5 | HG00438.hp2 NA18943.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-1108A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920291 | ||||||
chr2:227920481
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1051-918T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920481 | ||||||
chr2:227920676
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1051-723A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920676 | ||||||
chr2:227920708
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1051-691G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920708 | ||||||
chr2:227920722
|
G | T | 1 | a0001c0001t0001g0230 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1051-677G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920722 | ||||||
chr2:227920775
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1051-624T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920775 | ||||||
chr2:227920892
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1051-507C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920892 | ||||||
chr2:227920899
|
G | T | 1 | a0003c0004t0001g0312 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1051-500G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920899 | ||||||
chr2:227920980
|
G | T | 1 | a0001c0003t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1051-419G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920980 | ||||||
chr2:227921014
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1051-385A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227921014 | ||||||
chr2:227921015
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1051-384G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227921015 | ||||||
chr2:227921042
|
G | A | 1 | a0001c0003t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1051-357G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227921042 | ||||||
chr2:227921069
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1051-330A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227921069 | ||||||
chr2:227921087
|
G | A | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1051-312G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227921087 | ||||||
chr2:227921305
|
C | CT | 14 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(11): Show | 14 | HG01928.hp2 HG01934.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1051-66dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | |||||
chr2:227921305
|
CT | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0001g0058others(11): Show | 14 | HG00735.hp1 HG00735.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1051-66delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | |||||
chr2:227921305
|
CTT | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 83 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1051-67_1051-66del others(2): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | |||||
chr2:227921305
|
CTTT | C | 121 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0059others(118): Show | 125 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1051-68_1051-66del others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | |||||
chr2:227921305
|
CTTTT | C | 12 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(9): Show | 12 | HG00438.hp1 HG00642.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1051-69_1051-66del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | |||||
chr2:227921305
|
CTTTTT | C | 9 | a0001c0001t0001g0236a0001c0001t0001g0239a0001c0003t0002g0164others(6): Show | 9 | HG00738.hp2 HG01243.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051-70_1051-66del others(5): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | |||||
chr2:227921305
|
CTTTTTT | C | 15 | a0001c0003t0001g0316a0001c0003t0002g0153a0001c0003t0002g0154others(12): Show | 15 | HG00438.hp2 HG01891.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.1051-71_1051-66del others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | |||||
chr2:227921305
|
CTTTTTTT others(4): Show |
C | 3 | a0003c0004t0001g0308a0003c0004t0001g0310a0003c0004t0001g0315 | 3 | HG02976.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1051-76_1051-66del others(11): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | |||||
chr2:227921305
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0071 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1051-78_1051-66del others(13): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | |||||
chr2:227921845
|
C | T | 2 | a0001c0001t0001g0073a0003c0004t0001g0305 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1213+284C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227921845 | ||||||
chr2:227921887
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1213+326C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227921887 | ||||||
chr2:227921954
|
C | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.1213+393C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227921954 | ||||||
chr2:227922146
|
C | T | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1213+585C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922146 | ||||||
chr2:227922196
|
A | G | 1 | a0008c0008t0001g0323 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1213+635A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922196 | ||||||
chr2:227922200
|
G | A | 2 | a0001c0001t0001g0073a0003c0004t0001g0305 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1213+639G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922200 | ||||||
chr2:227922501
|
C | T | 1 | a0003c0004t0001g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1213+940C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922501 | ||||||
chr2:227922553
|
T | G | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1213+992T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922553 | ||||||
chr2:227922641
|
C | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 72 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1213+1080C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922641 | ||||||
chr2:227922641
|
C | T | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1213+1080C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922641 | ||||||
chr2:227922723
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1213+1162A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922723 | ||||||
chr2:227922730
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(260): Show | 272 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.1213+1169G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922730 | ||||||
chr2:227922817
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1214-1117A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922817 | ||||||
chr2:227922875
|
A | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(129): Show | 139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1214-1059A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922875 | ||||||
chr2:227922939
|
A | C | 1 | a0001c0001t0001g0193 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1214-995A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922939 | ||||||
chr2:227922945
|
C | G | 38 | a0001c0001t0001g0030a0001c0001t0001g0202a0001c0001t0001g0229others(35): Show | 41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1214-989C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922945 | ||||||
chr2:227923050
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1214-884A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923050 | ||||||
chr2:227923245
|
C | T | 1 | a0001c0003t0002g0177 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1214-689C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923245 | ||||||
chr2:227923289
|
C | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1214-645C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923289 | ||||||
chr2:227923485
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1214-449A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923485 | ||||||
chr2:227923493
|
T | A | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1214-441T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923493 | ||||||
chr2:227923542
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1214-392C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923542 | ||||||
chr2:227923574
|
A | G | 36 | a0001c0001t0001g0202a0001c0001t0001g0229a0001c0001t0001g0251others(33): Show | 39 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1214-360A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923574 | ||||||
chr2:227923615
|
A | C | 1 | a0001c0003t0001g0316 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1214-319A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923615 | ||||||
chr2:227923665
|
C | T | 38 | a0001c0001t0001g0030a0001c0001t0001g0202a0001c0001t0001g0229others(35): Show | 41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1214-269C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923665 | ||||||
chr2:227923678
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1214-256C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923678 | ||||||
chr2:227923730
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1214-204A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923730 | ||||||
chr2:227923742
|
C | T | 4 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0024others(1): Show | 4 | HG01884.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1214-192C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923742 | ||||||
chr2:227923745
|
GA | G | 27 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0204others(24): Show | 27 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1214-176delA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 227923745 | |||||
chr2:227923768
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1214-166T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923768 | ||||||
chr2:227923776
|
C | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0107 | 2 | NA18948.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1214-158C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923776 | ||||||
chr2:227923896
|
T | A | 6 | a0001c0003t0001g0298a0001c0003t0001g0300a0001c0003t0001g0301others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214-38T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923896 | ||||||
chr2:227923896
|
T | C | 3 | a0001c0001t0001g0198a0001c0003t0001g0297a0008c0008t0001g0323 | 3 | HG02717.hp1 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1214-38T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923896 |