geneid | 6670 |
---|---|
ensemblid | ENSG00000172845.18 |
hgncid | 11208 |
symbol | SP3 |
name | Sp3 transcription factor |
refseq_nuc | NM_003111.5 |
refseq_prot | NP_003102.1 |
ensembl_nuc | ENST00000310015.12 |
ensembl_prot | ENSP00000310301.6 |
mane_status | MANE Select |
chr | chr2 |
start | 173900775 |
end | 173965373 |
strand | - |
ver | v1.2 |
region | chr2:173900775-173965373 |
region5000 | chr2:173895775-173970373 |
regionname0 | SP3_chr2_173900775_173965373 |
regionname5000 | SP3_chr2_173895775_173970373 |
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 | 781 | 294 | 92 | 69 | 82 | 13 | 36 | 60 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002 | 0/0 | 781 | 58 | 0 | 5 | 48 | 1 | 4 | 40 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0003 | 0/0 | 781 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
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 | 2346 | 280 | 81 | 69 | 80 | 12 | 36 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
c0002 | 0/0 | 2346 | 58 | 0 | 5 | 48 | 1 | 4 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
c0003 | 0/0 | 2346 | 4 | 0 | 0 | 4 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
c0004 | 0/0 | 2346 | 4 | 4 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
c0005 | 0/0 | 2346 | 3 | 3 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
c0006 | 0/0 | 2346 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
c0007 | 0/0 | 2346 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
c0008 | 0/0 | 2346 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
c0009 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 9364 | 63 | 7 | 6 | 37 | 4 | 9 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0002 | 0/0 | 9368 | 39 | 0 | 5 | 32 | 1 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0003 | 0/0 | 9368 | 17 | 17 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0004 | 0/0 | 9365 | 17 | 1 | 0 | 16 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0005 | 0/0 | 9362 | 17 | 0 | 4 | 7 | 0 | 6 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0006 | 0/0 | 9368 | 15 | 2 | 5 | 6 | 1 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0007 | 0/0 | 9368 | 13 | 10 | 1 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0008 | 0/0 | 9364 | 13 | 5 | 3 | 2 | 1 | 2 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0009 | 0/0 | 9365 | 9 | 3 | 5 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0010 | 0/0 | 9367 | 7 | 7 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0011 | 0/0 | 9361 | 7 | 4 | 3 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0012 | 0/0 | 9366 | 7 | 0 | 2 | 2 | 0 | 3 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0013 | 0/0 | 9369 | 6 | 0 | 0 | 5 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0014 | 0/1 | 9368 | 6 | 1 | 1 | 0 | 2 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0015 | 0/0 | 9368 | 6 | 0 | 5 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0016 | 0/0 | 9371 | 6 | 0 | 5 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0017 | 0/0 | 9364 | 5 | 1 | 4 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0018 | 0/0 | 9366 | 3 | 3 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0019 | 0/0 | 9368 | 3 | 0 | 0 | 3 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0020 | 0/0 | 9368 | 3 | 0 | 0 | 2 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0021 | 0/0 | 9369 | 3 | 0 | 1 | 0 | 0 | 2 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0022 | 0/0 | 9360 | 3 | 3 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0023 | 0/0 | 9371 | 2 | 0 | 2 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0024 | 0/0 | 9369 | 2 | 0 | 1 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0025 | 0/0 | 9369 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0026 | 0/0 | 9364 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0027 | 0/0 | 9365 | 2 | 1 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0028 | 0/0 | 9364 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0029 | 0/0 | 9366 | 2 | 0 | 0 | 0 | 0 | 2 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0030 | 0/0 | 9364 | 2 | 0 | 0 | 0 | 2 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0031 | 0/0 | 9364 | 2 | 0 | 2 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0032 | 0/0 | 9361 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0033 | 0/0 | 9366 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0034 | 0/0 | 9362 | 2 | 1 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0035 | 0/0 | 9368 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0036 | 0/0 | 9365 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0037 | 0/0 | 9366 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0038 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0039 | 0/0 | 9368 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0040 | 0/0 | 9369 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0041 | 0/0 | 9370 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0042 | 0/0 | 9364 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0043 | 0/0 | 9369 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0044 | 0/0 | 9369 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0045 | 0/0 | 9367 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0046 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0047 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0048 | 0/0 | 9364 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0049 | 0/0 | 9368 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0050 | 0/0 | 9371 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0051 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0052 | 0/0 | 9369 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0053 | 0/0 | 9361 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0054 | 0/0 | 9362 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0055 | 0/0 | 9364 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0056 | 0/0 | 9364 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0057 | 0/0 | 9365 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0058 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0059 | 0/0 | 9369 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0060 | 0/0 | 9365 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0061 | 1/0 | 9369 | 1 | 0 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0062 | 0/0 | 9364 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0063 | 0/0 | 9364 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0064 | 0/0 | 9368 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0065 | 0/0 | 9364 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0066 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0067 | 0/0 | 9364 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0068 | 0/0 | 9367 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0069 | 0/0 | 9364 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0070 | 0/0 | 9368 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0071 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0072 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0073 | 0/0 | 9364 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0074 | 0/0 | 9367 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0075 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0076 | 0/0 | 9367 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0077 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0078 | 0/0 | 9362 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0079 | 0/0 | 9361 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0080 | 0/0 | 9363 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0081 | 0/0 | 9362 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0082 | 0/0 | 9363 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0083 | 0/0 | 9362 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0084 | 0/0 | 9362 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0085 | 0/0 | 9368 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0086 | 0/0 | 9360 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0087 | 0/0 | 9361 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0088 | 0/0 | 9361 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0089 | 0/0 | 9360 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0090 | 0/0 | 9367 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0091 | 0/0 | 9364 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0092 | 0/0 | 9371 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0093 | 0/0 | 9370 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0094 | 0/0 | 9364 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0095 | 0/0 | 9364 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0096 | 0/0 | 9362 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0097 | 0/0 | 9367 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
t0098 | 0/0 | 9367 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
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 | 3 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
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 | 2346 | 280 | 81 | 69 | 80 | 12 | 36 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0004 | 0/0 | 2346 | 4 | 4 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0005 | 0/0 | 2346 | 3 | 3 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0006 | 0/0 | 2346 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0007 | 0/0 | 2346 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0008 | 0/0 | 2346 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0009 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002 | 0/0 | 2346 | 58 | 0 | 5 | 48 | 1 | 4 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0003c0003 | 0/0 | 2346 | 4 | 0 | 0 | 4 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11709 | 63 | 7 | 6 | 37 | 4 | 9 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0003 | 0/0 | 11713 | 15 | 15 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0004 | 0/0 | 11710 | 13 | 1 | 0 | 12 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0005 | 0/0 | 11707 | 17 | 0 | 4 | 7 | 0 | 6 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0006 | 0/0 | 11713 | 13 | 2 | 5 | 4 | 1 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0007 | 0/0 | 11713 | 9 | 6 | 1 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0008 | 0/0 | 11709 | 11 | 3 | 3 | 2 | 1 | 2 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0009 | 0/0 | 11710 | 9 | 3 | 5 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0010 | 0/0 | 11712 | 7 | 7 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0011 | 0/0 | 11706 | 7 | 4 | 3 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0012 | 0/0 | 11711 | 7 | 0 | 2 | 2 | 0 | 3 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0014 | 0/1 | 11713 | 5 | 1 | 1 | 0 | 1 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0015 | 0/0 | 11713 | 6 | 0 | 5 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0016 | 0/0 | 11716 | 6 | 0 | 5 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0017 | 0/0 | 11709 | 5 | 1 | 4 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0018 | 0/0 | 11711 | 3 | 3 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0021 | 0/0 | 11714 | 3 | 0 | 1 | 0 | 0 | 2 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0022 | 0/0 | 11705 | 3 | 3 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0023 | 0/0 | 11716 | 2 | 0 | 2 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0024 | 0/0 | 11714 | 2 | 0 | 1 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0025 | 0/0 | 11714 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0026 | 0/0 | 11709 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0027 | 0/0 | 11710 | 2 | 1 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0028 | 0/0 | 11709 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0029 | 0/0 | 11711 | 2 | 0 | 0 | 0 | 0 | 2 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0030 | 0/0 | 11709 | 2 | 0 | 0 | 0 | 2 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0031 | 0/0 | 11709 | 2 | 0 | 2 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0032 | 0/0 | 11706 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0033 | 0/0 | 11711 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0034 | 0/0 | 11707 | 2 | 1 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0035 | 0/0 | 11713 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0036 | 0/0 | 11710 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0037 | 0/0 | 11711 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0038 | 0/0 | 11713 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0039 | 0/0 | 11713 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0040 | 0/0 | 11714 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0046 | 0/0 | 11713 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0047 | 0/0 | 11713 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0048 | 0/0 | 11709 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0049 | 0/0 | 11713 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0050 | 0/0 | 11716 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0051 | 0/0 | 11714 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0053 | 0/0 | 11706 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0054 | 0/0 | 11707 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0055 | 0/0 | 11709 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0056 | 0/0 | 11709 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0057 | 0/0 | 11710 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0059 | 0/0 | 11714 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0060 | 0/0 | 11710 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0061 | 1/0 | 11714 | 1 | 0 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0062 | 0/0 | 11709 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0063 | 0/0 | 11709 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0064 | 0/0 | 11713 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0065 | 0/0 | 11709 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0066 | 0/0 | 11713 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0067 | 0/0 | 11709 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0068 | 0/0 | 11712 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0069 | 0/0 | 11709 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0070 | 0/0 | 11713 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0071 | 0/0 | 11713 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0072 | 0/0 | 11713 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0073 | 0/0 | 11709 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0075 | 0/0 | 11713 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0076 | 0/0 | 11712 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0077 | 0/0 | 11714 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0078 | 0/0 | 11707 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0079 | 0/0 | 11706 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0080 | 0/0 | 11708 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0081 | 0/0 | 11707 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0082 | 0/0 | 11708 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0083 | 0/0 | 11707 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0084 | 0/0 | 11707 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0085 | 0/0 | 11713 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0086 | 0/0 | 11705 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0087 | 0/0 | 11706 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0088 | 0/0 | 11706 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0089 | 0/0 | 11705 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0090 | 0/0 | 11712 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0091 | 0/0 | 11709 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0092 | 0/0 | 11716 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0093 | 0/0 | 11715 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0094 | 0/0 | 11709 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0095 | 0/0 | 11709 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0001t0096 | 0/0 | 11707 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0004t0007 | 0/0 | 11713 | 4 | 4 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0005t0074 | 0/0 | 11712 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0005t0097 | 0/0 | 11712 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0005t0098 | 0/0 | 11712 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0006t0006 | 0/0 | 11713 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0007t0008 | 0/0 | 11709 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0008t0003 | 0/0 | 11713 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0001c0009t0014 | 0/0 | 11713 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0002 | 0/0 | 11713 | 39 | 0 | 5 | 32 | 1 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0013 | 0/0 | 11714 | 6 | 0 | 0 | 5 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0019 | 0/0 | 11713 | 3 | 0 | 0 | 3 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0020 | 0/0 | 11713 | 3 | 0 | 0 | 2 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0041 | 0/0 | 11715 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0042 | 0/0 | 11709 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0043 | 0/0 | 11714 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0044 | 0/0 | 11714 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0045 | 0/0 | 11712 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0052 | 0/0 | 11714 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0002c0002t0058 | 0/0 | 11713 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
a0003c0003t0004 | 0/0 | 11710 | 4 | 0 | 0 | 4 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | copy fasta | chr2 | 173895775 | 173970373 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0007g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0008g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0008g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0008g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0009g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0009g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0009g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0010g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0010g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0010g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0011g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0011g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0011g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0012g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0012g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0012g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0012g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0012g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0012g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0012g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0014g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0014g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0014g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0014g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0014g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0015g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0015g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0015g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0015g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0015g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0015g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0016g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0016g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0016g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0016g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0016g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0016g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0017g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0017g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0017g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0017g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0018g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0018g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0018g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0021g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0021g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0021g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0022g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0022g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0022g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0023g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0023g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0024g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0024g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0025g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0026g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0026g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0027g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0027g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0028g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0028g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0029g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0029g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0030g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0030g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0031g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0032g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0032g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0033g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0033g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0034g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0034g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0035g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0036g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0037g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0038g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0039g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0040g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0046g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0047g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0048g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0049g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0050g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0051g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0053g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0054g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0055g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0056g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0057g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0059g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0060g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0061g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0062g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0063g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0064g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0065g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0066g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0067g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0068g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0069g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0070g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0071g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0072g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0073g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0075g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0076g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0077g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0078g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0079g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0080g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0081g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0082g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0083g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0084g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0085g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0086g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0087g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0088g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0089g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0090g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0091g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0092g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0093g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0094g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0095g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0001t0096g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0004t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0004t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0004t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0004t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0005t0074g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0005t0097g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0005t0098g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0006t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0006t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0007t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0007t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0008t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0008t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0001c0009t0014g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0013g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0013g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0013g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0013g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0013g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0013g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0019g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0019g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0019g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0020g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0020g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0020g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0041g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0042g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0043g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0044g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0045g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0052g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0002c0002t0058g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0003c0003t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0003c0003t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0003c0003t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
a0003c0003t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0286 | EUR | GBR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00099 | hp2 | a0001 | c0001 | t0008 | g0005 | EUR | GBR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00140 | hp1 | a0001 | c0001 | t0016 | g0232 | EUR | GBR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00140 | hp2 | a0001 | c0001 | t0014 | g0245 | EUR | GBR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00323 | hp1 | a0001 | c0001 | t0050 | g0230 | EUR | FIN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00408 | hp2 | a0002 | c0002 | t0058 | g0335 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00438 | hp2 | a0001 | c0001 | t0090 | g0296 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00597 | hp1 | a0001 | c0001 | t0062 | g0074 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00597 | hp2 | a0001 | c0001 | t0057 | g0093 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00609 | hp1 | a0001 | c0001 | t0091 | g0337 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00621 | hp1 | a0001 | c0001 | t0012 | g0295 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00639 | hp1 | a0001 | c0001 | t0073 | g0080 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00639 | hp2 | a0001 | c0001 | t0016 | g0229 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0065 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00642 | hp2 | a0001 | c0001 | t0014 | g0067 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00735 | hp1 | a0001 | c0001 | t0034 | g0021 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00735 | hp2 | a0001 | c0001 | t0036 | g0324 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00738 | hp1 | a0001 | c0001 | t0016 | g0227 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00741 | hp1 | a0001 | c0001 | t0088 | g0051 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG00741 | hp2 | a0001 | c0001 | t0015 | g0311 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01070 | hp1 | a0001 | c0001 | t0093 | g0224 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0112 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01071 | hp1 | a0001 | c0001 | t0092 | g0223 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0124 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01074 | hp2 | a0001 | c0001 | t0016 | g0225 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01081 | hp1 | a0001 | c0001 | t0016 | g0228 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01099 | hp1 | a0001 | c0001 | t0056 | g0175 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0110 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01106 | hp1 | a0001 | c0001 | t0082 | g0054 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01167 | hp1 | a0001 | c0001 | t0023 | g0226 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0123 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01168 | hp1 | a0001 | c0001 | t0008 | g0183 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01168 | hp2 | a0001 | c0001 | t0011 | g0055 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01169 | hp1 | a0001 | c0001 | t0011 | g0056 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01169 | hp2 | a0001 | c0001 | t0023 | g0231 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01175 | hp1 | a0001 | c0001 | t0084 | g0041 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01175 | hp2 | a0001 | c0001 | t0080 | g0032 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01243 | hp1 | a0001 | c0001 | t0040 | g0222 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0327 | AMR | PUR | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01255 | hp1 | a0001 | c0001 | t0031 | g0008 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01255 | hp2 | a0001 | c0001 | t0021 | g0274 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0113 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01257 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0037 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01258 | hp2 | a0001 | c0001 | t0009 | g0001 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01261 | hp1 | a0001 | c0001 | t0012 | g0298 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01261 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01346 | hp1 | a0001 | c0001 | t0015 | g0307 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01346 | hp2 | a0001 | c0001 | t0012 | g0297 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01361 | hp1 | a0001 | c0001 | t0095 | g0079 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0217 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01433 | hp1 | a0001 | c0001 | t0078 | g0039 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01433 | hp2 | a0001 | c0001 | t0009 | g0082 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01496 | hp1 | a0001 | c0001 | t0015 | g0320 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01496 | hp2 | a0001 | c0001 | t0067 | g0199 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0107 | EUR | IBS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01515 | hp2 | a0001 | c0001 | t0030 | g0184 | EUR | IBS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01517 | hp1 | a0001 | c0009 | t0014 | g0243 | EUR | IBS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01517 | hp2 | a0001 | c0001 | t0030 | g0173 | EUR | IBS | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01884 | hp1 | a0001 | c0001 | t0010 | g0100 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01884 | hp2 | a0001 | c0004 | t0007 | g0319 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01891 | hp1 | a0001 | c0008 | t0003 | g0235 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01928 | hp1 | a0001 | c0001 | t0037 | g0083 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01934 | hp1 | a0001 | c0001 | t0064 | g0309 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01934 | hp2 | a0001 | c0001 | t0069 | g0178 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01943 | hp1 | a0001 | c0001 | t0017 | g0006 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01952 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01952 | hp2 | a0001 | c0001 | t0017 | g0006 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01975 | hp1 | a0001 | c0001 | t0017 | g0172 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01975 | hp2 | a0001 | c0001 | t0016 | g0291 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01978 | hp1 | a0001 | c0001 | t0031 | g0008 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01978 | hp2 | a0001 | c0001 | t0024 | g0219 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01981 | hp1 | a0001 | c0001 | t0094 | g0180 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0241 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01993 | hp1 | a0001 | c0001 | t0039 | g0308 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02056 | hp1 | a0002 | c0002 | t0013 | g0211 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02056 | hp2 | a0001 | c0001 | t0028 | g0062 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02074 | hp1 | a0002 | c0002 | t0013 | g0264 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02074 | hp2 | a0001 | c0001 | t0028 | g0128 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02080 | hp1 | a0001 | c0001 | t0066 | g0114 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0265 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02145 | hp2 | a0001 | c0001 | t0083 | g0040 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02165 | hp2 | a0001 | c0001 | t0060 | g0125 | EAS | CDX | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02257 | hp2 | a0001 | c0005 | t0074 | g0191 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02258 | hp1 | a0001 | c0001 | t0071 | g0102 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02258 | hp2 | a0001 | c0001 | t0046 | g0287 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02273 | hp2 | a0001 | c0001 | t0015 | g0310 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0133 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02280 | hp2 | a0001 | c0001 | t0032 | g0014 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02293 | hp1 | a0001 | c0001 | t0017 | g0181 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02293 | hp2 | a0001 | c0001 | t0015 | g0068 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02300 | hp2 | a0001 | c0001 | t0009 | g0084 | AMR | PEL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02451 | hp2 | a0001 | c0001 | t0087 | g0044 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02523 | hp1 | a0002 | c0002 | t0044 | g0239 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02523 | hp2 | a0001 | c0001 | t0063 | g0104 | EAS | KHV | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0098 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0092 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02602 | hp1 | a0001 | c0001 | t0081 | g0018 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02615 | hp1 | a0001 | c0001 | t0076 | g0097 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02615 | hp2 | a0001 | c0001 | t0010 | g0096 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02630 | hp1 | a0001 | c0007 | t0008 | g0136 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0135 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02647 | hp2 | a0001 | c0001 | t0051 | g0275 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0118 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0038 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02717 | hp1 | a0001 | c0001 | t0053 | g0045 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02717 | hp2 | a0001 | c0001 | t0018 | g0323 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02738 | hp1 | a0001 | c0001 | t0024 | g0207 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02738 | hp2 | a0002 | c0002 | t0013 | g0218 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02809 | hp1 | a0001 | c0004 | t0007 | g0317 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02818 | hp1 | a0001 | c0001 | t0010 | g0312 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02818 | hp2 | a0001 | c0001 | t0034 | g0022 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02895 | hp1 | a0001 | c0001 | t0086 | g0058 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02895 | hp2 | a0001 | c0005 | t0098 | g0340 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02896 | hp1 | a0001 | c0001 | t0032 | g0050 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0122 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02897 | hp1 | a0001 | c0005 | t0097 | g0341 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0120 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02922 | hp2 | a0001 | c0001 | t0025 | g0012 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0043 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0033 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03041 | hp2 | a0001 | c0001 | t0022 | g0049 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03098 | hp1 | a0001 | c0001 | t0038 | g0290 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0085 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03130 | hp1 | a0001 | c0007 | t0008 | g0105 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03139 | hp1 | a0001 | c0001 | t0022 | g0046 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03139 | hp2 | a0001 | c0001 | t0025 | g0012 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03195 | hp2 | a0001 | c0001 | t0089 | g0048 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03209 | hp1 | a0001 | c0001 | t0096 | g0301 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03209 | hp2 | a0001 | c0001 | t0077 | g0190 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0134 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03239 | hp2 | a0001 | c0001 | t0070 | g0089 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03486 | hp2 | a0001 | c0001 | t0022 | g0047 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03490 | hp2 | a0002 | c0002 | t0020 | g0269 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03491 | hp1 | a0001 | c0001 | t0012 | g0299 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03491 | hp2 | a0001 | c0001 | t0014 | g0246 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03492 | hp2 | a0001 | c0001 | t0012 | g0300 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0015 | AFR | ESN | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03540 | hp1 | a0001 | c0001 | t0009 | g0087 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03540 | hp2 | a0001 | c0001 | t0075 | g0288 | AFR | GWD | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03579 | hp1 | a0001 | c0001 | t0010 | g0328 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03654 | hp1 | a0001 | c0001 | t0065 | g0143 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0017 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03688 | hp1 | a0001 | c0001 | t0048 | g0202 | SAS | STU | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03704 | hp2 | a0001 | c0001 | t0008 | g0095 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03710 | hp1 | a0001 | c0001 | t0015 | g0306 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0035 | SAS | PJL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03831 | hp1 | a0001 | c0001 | t0009 | g0081 | SAS | BEB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03831 | hp2 | a0001 | c0001 | t0029 | g0131 | SAS | BEB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | BEB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03834 | hp2 | a0001 | c0001 | t0049 | g0203 | SAS | BEB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG04115 | hp1 | a0001 | c0001 | t0029 | g0063 | SAS | STU | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0260 | SAS | STU | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG04184 | hp1 | a0001 | c0001 | t0021 | g0059 | SAS | BEB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG04184 | hp2 | a0001 | c0001 | t0079 | g0019 | SAS | BEB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG04199 | hp1 | a0001 | c0001 | t0021 | g0221 | SAS | STU | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG04199 | hp2 | a0001 | c0001 | t0035 | g0088 | SAS | STU | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0016 | SAS | STU | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG04228 | hp2 | a0001 | c0001 | t0012 | g0293 | SAS | STU | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | YRI | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18522 | hp2 | a0001 | c0001 | t0055 | g0091 | AFR | YRI | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0192 | EAS | CHB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18906 | hp1 | a0001 | c0001 | t0014 | g0325 | AFR | YRI | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18906 | hp2 | a0001 | c0004 | t0007 | g0318 | AFR | YRI | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18939 | hp2 | a0002 | c0002 | t0019 | g0237 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18950 | hp1 | a0001 | c0001 | t0033 | g0066 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18953 | hp1 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18956 | hp2 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18959 | hp2 | a0001 | c0001 | t0027 | g0160 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18965 | hp2 | a0003 | c0003 | t0004 | g0315 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18971 | hp1 | a0002 | c0002 | t0042 | g0204 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18972 | hp1 | a0002 | c0002 | t0019 | g0253 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18974 | hp2 | a0001 | c0001 | t0012 | g0292 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18977 | hp1 | a0002 | c0002 | t0020 | g0266 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18978 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18979 | hp2 | a0002 | c0002 | t0043 | g0209 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18982 | hp1 | a0002 | c0002 | t0020 | g0252 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18985 | hp1 | a0001 | c0001 | t0008 | g0161 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18985 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18994 | hp1 | a0003 | c0003 | t0004 | g0069 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18995 | hp2 | a0002 | c0002 | t0041 | g0336 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19002 | hp1 | a0001 | c0001 | t0007 | g0119 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19006 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19006 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | LWK | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19030 | hp2 | a0001 | c0001 | t0047 | g0072 | AFR | LWK | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19043 | hp1 | a0001 | c0001 | t0011 | g0053 | AFR | LWK | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | LWK | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19056 | hp1 | a0001 | c0001 | t0072 | g0116 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19058 | hp2 | a0001 | c0001 | t0059 | g0075 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19060 | hp1 | a0002 | c0002 | t0019 | g0073 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19060 | hp2 | a0003 | c0003 | t0004 | g0314 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19065 | hp1 | a0003 | c0003 | t0004 | g0313 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19067 | hp1 | a0002 | c0002 | t0045 | g0254 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19068 | hp1 | a0001 | c0001 | t0033 | g0294 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19068 | hp2 | a0001 | c0006 | t0006 | g0109 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19077 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19078 | hp1 | a0002 | c0002 | t0013 | g0206 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19081 | hp1 | a0001 | c0006 | t0006 | g0108 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19082 | hp2 | a0002 | c0002 | t0013 | g0213 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19086 | hp2 | a0002 | c0002 | t0013 | g0267 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19240 | hp1 | a0001 | c0001 | t0018 | g0321 | AFR | YRI | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA19240 | hp2 | a0001 | c0001 | t0026 | g0339 | AFR | YRI | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA20129 | hp1 | a0001 | c0001 | t0009 | g0086 | AFR | ASW | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0101 | AFR | ASW | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA20805 | hp2 | a0001 | c0001 | t0054 | g0034 | EUR | TSI | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA20905 | hp1 | a0001 | c0001 | t0008 | g0094 | SAS | GIH | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA20905 | hp2 | a0002 | c0002 | t0052 | g0268 | SAS | GIH | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01123 | hp1 | a0001 | c0001 | t0011 | g0052 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG01123 | hp2 | a0001 | c0001 | t0008 | g0166 | AMR | CLM | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02109 | hp1 | a0001 | c0004 | t0007 | g0316 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02109 | hp2 | a0001 | c0008 | t0003 | g0236 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02486 | hp1 | a0001 | c0001 | t0026 | g0338 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02486 | hp2 | a0001 | c0001 | t0027 | g0140 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02559 | hp1 | a0001 | c0001 | t0018 | g0322 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | ACB | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0139 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0057 | AFR | MSL | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG06807 | hp1 | a0001 | c0001 | t0085 | g0042 | AFR | USA | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
HG06807 | hp2 | a0001 | c0001 | t0017 | g0164 | AFR | USA | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA21309 | hp1 | a0001 | c0001 | t0010 | g0099 | AFR | LWK | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
NA21309 | hp2 | a0001 | c0001 | t0068 | g0289 | AFR | LWK | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0014 | g0071 | REF | REF | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0061 | g0281 | REF | REF | SP3_chr2_173895775_173970373 | SP3 | chr2 | 173895775 | 173970373 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:173956022
|
T | C | 1 | a0002 | 58 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(55): Show |
missense_variant | MODERATE | c.490A>G | p.Thr164Ala | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/7 | 692/11714 | 490/2346 | 164/781 | chr2 | 173956022 | ||
chr2:173964503
|
T | C | 1 | a0003 | 4 | NA18965.hp2 NA18994.hp1 NA19060.hp2 others(1): Show |
missense_variant | MODERATE | c.58A>G | p.Ser20Gly | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 2/7 | 260/11714 | 58/2346 | 20/781 | chr2 | 173964503 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:173910145
|
T | G | 1 | a0001c0007 | 2 | HG02630.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.2142A>C | p.Thr714Thr | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 2344/11714 | 2142/2346 | 714/781 | chr2 | 173910145 | ||
chr2:173954946
|
T | C | 1 | a0001c0007 | 2 | HG02630.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.1566A>G | p.Gln522Gln | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/7 | 1768/11714 | 1566/2346 | 522/781 | chr2 | 173954946 | ||
chr2:173954985
|
A | C | 1 | a0001c0009 | 1 | HG01517.hp1 | synonymous_variant | LOW | c.1527T>G | p.Thr509Thr | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/7 | 1729/11714 | 1527/2346 | 509/781 | chr2 | 173954985 | ||
chr2:173955312
|
A | C | 1 | a0001c0005 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.1200T>G | p.Leu400Leu | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/7 | 1402/11714 | 1200/2346 | 400/781 | chr2 | 173955312 | ||
chr2:173955438
|
T | A | 1 | a0001c0008 | 2 | HG01891.hp1 HG02109.hp2 |
synonymous_variant | LOW | c.1074A>T | p.Thr358Thr | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/7 | 1276/11714 | 1074/2346 | 358/781 | chr2 | 173955438 | ||
chr2:173955894
|
G | T | 1 | a0001c0006 | 2 | NA19068.hp2 NA19081.hp1 |
synonymous_variant | LOW | c.618C>A | p.Ile206Ile | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/7 | 820/11714 | 618/2346 | 206/781 | chr2 | 173955894 | ||
chr2:173964516
|
G | A | 1 | a0001c0004 | 4 | HG01884.hp2 HG02109.hp1 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.45C>T | p.Ala15Ala | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 2/7 | 247/11714 | 45/2346 | 15/781 | chr2 | 173964516 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:173900922
|
G | A | 5 | a0001c0001t0011a0001c0001t0082a0001c0001t0084others(2): Show | 11 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9019C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 9019 | chr2 | 173900922 | |||||
chr2:173901065
|
A | G | 12 | a0001c0001t0011a0001c0001t0022a0001c0001t0032others(9): Show | 21 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*8876T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8876 | chr2 | 173901065 | |||||
chr2:173901193
|
AAGAT | A | 46 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(43): Show | 170 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*8744_*8747delATCT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8744 | chr2 | 173901193 | |||||
chr2:173901230
|
C | G | 4 | a0001c0001t0009a0001c0001t0035a0001c0001t0036others(1): Show | 12 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*8711G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8711 | chr2 | 173901230 | |||||
chr2:173901259
|
TTTC | T | 19 | a0001c0001t0005a0001c0001t0011a0001c0001t0022others(16): Show | 45 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*8679_*8681delGAA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8679 | chr2 | 173901259 | |||||
chr2:173901470
|
A | G | 1 | a0001c0005t0097 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8471T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8471 | chr2 | 173901470 | |||||
chr2:173901645
|
C | T | 1 | a0001c0001t0062 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8296G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8296 | chr2 | 173901645 | |||||
chr2:173901695
|
C | CT | 8 | a0001c0001t0029a0001c0001t0035a0001c0001t0075others(5): Show | 9 | HG00438.hp2 HG01070.hp1 HG01106.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8245dupA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8245 | chr2 | 173901695 | |||||
chr2:173901695
|
C | CTT | 4 | a0001c0001t0016a0001c0001t0023a0001c0001t0050others(1): Show | 10 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*8244_*8245dupAA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8245 | chr2 | 173901695 | |||||
chr2:173901695
|
CT | C | 52 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(49): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*8245delA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8245 | chr2 | 173901695 | |||||
chr2:173901695
|
CTT | C | 7 | a0001c0001t0009a0001c0001t0022a0001c0001t0036others(4): Show | 17 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*8244_*8245delAA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8244 | chr2 | 173901695 | |||||
chr2:173901931
|
G | A | 1 | a0001c0001t0069 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8010C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 8010 | chr2 | 173901931 | |||||
chr2:173902065
|
C | G | 4 | a0001c0001t0009a0001c0001t0035a0001c0001t0036others(1): Show | 12 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7876G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 7876 | chr2 | 173902065 | |||||
chr2:173902368
|
T | C | 1 | a0001c0001t0050 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7573A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 7573 | chr2 | 173902368 | |||||
chr2:173902480
|
A | G | 4 | a0001c0001t0009a0001c0001t0035a0001c0001t0036others(1): Show | 12 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7461T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 7461 | chr2 | 173902480 | |||||
chr2:173902735
|
G | A | 4 | a0001c0001t0009a0001c0001t0035a0001c0001t0036others(1): Show | 12 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7206C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 7206 | chr2 | 173902735 | |||||
chr2:173902906
|
G | A | 4 | a0001c0001t0009a0001c0001t0035a0001c0001t0036others(1): Show | 12 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7035C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 7035 | chr2 | 173902906 | |||||
chr2:173902907
|
A | C | 2 | a0001c0001t0026a0001c0001t0055 | 3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7034T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 7034 | chr2 | 173902907 | |||||
chr2:173902935
|
T | C | 11 | a0001c0001t0015a0001c0001t0016a0001c0001t0021others(8): Show | 24 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7006A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 7006 | chr2 | 173902935 | |||||
chr2:173902937
|
G | A | 1 | a0001c0001t0063 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7004C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 7004 | chr2 | 173902937 | |||||
chr2:173902991
|
T | C | 1 | a0001c0001t0057 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6950A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 6950 | chr2 | 173902991 | |||||
chr2:173903349
|
T | G | 1 | a0001c0001t0078 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6592A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 6592 | chr2 | 173903349 | |||||
chr2:173903373
|
G | A | 96 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(93): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*6568C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 6568 | chr2 | 173903373 | |||||
chr2:173903441
|
T | C | 11 | a0001c0001t0015a0001c0001t0016a0001c0001t0021others(8): Show | 24 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6500A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 6500 | chr2 | 173903441 | |||||
chr2:173903510
|
T | C | 1 | a0001c0001t0072 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6431A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 6431 | chr2 | 173903510 | |||||
chr2:173903565
|
G | A | 2 | a0001c0001t0025a0001c0001t0046 | 3 | HG02258.hp2 HG02922.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6376C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 6376 | chr2 | 173903565 | |||||
chr2:173903762
|
T | C | 1 | a0001c0001t0065 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6179A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 6179 | chr2 | 173903762 | |||||
chr2:173903927
|
A | T | 1 | a0001c0001t0060 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6014T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 6014 | chr2 | 173903927 | |||||
chr2:173903936
|
C | A | 1 | a0001c0001t0076 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6005G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 6005 | chr2 | 173903936 | |||||
chr2:173904121
|
A | T | 8 | a0001c0001t0005a0001c0001t0030a0001c0001t0034others(5): Show | 26 | HG00639.hp1 HG00735.hp1 HG01081.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5820T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5820 | chr2 | 173904121 | |||||
chr2:173904249
|
T | C | 1 | a0001c0001t0036 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5692A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5692 | chr2 | 173904249 | |||||
chr2:173904273
|
C | T | 1 | a0001c0001t0077 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5668G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5668 | chr2 | 173904273 | |||||
chr2:173904341
|
G | A | 1 | a0001c0001t0066 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5600C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5600 | chr2 | 173904341 | |||||
chr2:173904388
|
G | C | 1 | a0001c0001t0067 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5553C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5553 | chr2 | 173904388 | |||||
chr2:173904431
|
GTC | G | 6 | a0001c0001t0010a0001c0001t0075a0001c0001t0076others(3): Show | 12 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5508_*5509delGA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5508 | chr2 | 173904431 | |||||
chr2:173904478
|
GA | G | 5 | a0001c0001t0012a0001c0001t0028a0001c0001t0033others(2): Show | 13 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5462delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5462 | chr2 | 173904478 | |||||
chr2:173904480
|
A | C | 1 | a0001c0001t0047 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5461T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5461 | chr2 | 173904480 | |||||
chr2:173904490
|
G | A | 3 | a0002c0002t0019a0002c0002t0043a0002c0002t0045 | 5 | NA18939.hp2 NA18972.hp1 NA18979.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5451C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5451 | chr2 | 173904490 | |||||
chr2:173904561
|
T | C | 1 | a0001c0001t0071 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5380A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5380 | chr2 | 173904561 | |||||
chr2:173904616
|
C | T | 51 | a0001c0001t0007a0001c0001t0008a0001c0001t0010others(48): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*5325G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5325 | chr2 | 173904616 | |||||
chr2:173904750
|
G | A | 1 | a0001c0001t0068 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5191C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5191 | chr2 | 173904750 | |||||
chr2:173904807
|
T | C | 1 | a0002c0002t0045 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5134A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5134 | chr2 | 173904807 | |||||
chr2:173904843
|
T | C | 3 | a0001c0001t0017a0001c0001t0037a0001c0001t0069 | 7 | HG01928.hp1 HG01934.hp2 HG01943.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5098A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 5098 | chr2 | 173904843 | |||||
chr2:173904945
|
G | A | 5 | a0001c0001t0009a0001c0001t0018a0001c0001t0035others(2): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4996C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4996 | chr2 | 173904945 | |||||
chr2:173904946
|
C | G | 11 | a0002c0002t0002a0002c0002t0013a0002c0002t0019others(8): Show | 58 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*4995G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4995 | chr2 | 173904946 | |||||
chr2:173905097
|
A | G | 1 | a0001c0001t0040 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4844T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4844 | chr2 | 173905097 | |||||
chr2:173905232
|
C | A | 1 | a0001c0001t0051 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4709G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4709 | chr2 | 173905232 | |||||
chr2:173905433
|
A | G | 1 | a0001c0001t0039 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4508T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4508 | chr2 | 173905433 | |||||
chr2:173905450
|
C | A | 4 | a0001c0001t0010a0001c0001t0075a0001c0001t0076others(1): Show | 10 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4491G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4491 | chr2 | 173905450 | |||||
chr2:173905561
|
G | A | 3 | a0001c0001t0012a0001c0001t0033a0001c0001t0090 | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4380C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4380 | chr2 | 173905561 | |||||
chr2:173905598
|
TGAC | T | 3 | a0001c0001t0012a0001c0001t0033a0001c0001t0090 | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4340_*4342delGTC | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4340 | chr2 | 173905598 | |||||
chr2:173905615
|
C | A | 30 | a0001c0001t0003a0001c0001t0014a0001c0001t0015others(27): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*4326G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4326 | chr2 | 173905615 | |||||
chr2:173905651
|
A | G | 1 | a0001c0001t0057 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4290T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4290 | chr2 | 173905651 | |||||
chr2:173905677
|
G | GA | 6 | a0001c0001t0009a0001c0001t0018a0001c0001t0035others(3): Show | 16 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4263dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4263 | chr2 | 173905677 | |||||
chr2:173905722
|
A | G | 8 | a0001c0001t0009a0001c0001t0012a0001c0001t0018others(5): Show | 25 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4219T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4219 | chr2 | 173905722 | |||||
chr2:173905777
|
T | A | 1 | a0001c0001t0033 | 2 | NA18950.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4164A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4164 | chr2 | 173905777 | |||||
chr2:173905791
|
G | A | 1 | a0001c0001t0089 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4150C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4150 | chr2 | 173905791 | |||||
chr2:173905926
|
G | A | 1 | a0001c0001t0070 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4015C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4015 | chr2 | 173905926 | |||||
chr2:173905935
|
G | A | 5 | a0001c0001t0009a0001c0001t0018a0001c0001t0035others(2): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4006C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 4006 | chr2 | 173905935 | |||||
chr2:173906035
|
T | C | 1 | a0001c0001t0071 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3906A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 3906 | chr2 | 173906035 | |||||
chr2:173906155
|
TCCC | T | 5 | a0001c0001t0009a0001c0001t0018a0001c0001t0035others(2): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3783_*3785delGGG | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 3783 | chr2 | 173906155 | |||||
chr2:173906366
|
T | A | 1 | a0001c0001t0072 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3575A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 3575 | chr2 | 173906366 | |||||
chr2:173906368
|
A | C | 1 | a0001c0001t0056 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3573T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 3573 | chr2 | 173906368 | |||||
chr2:173906768
|
A | G | 1 | a0001c0001t0055 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3173T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 3173 | chr2 | 173906768 | |||||
chr2:173906814
|
T | C | 7 | a0001c0001t0010a0001c0001t0075a0001c0001t0076others(4): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3127A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 3127 | chr2 | 173906814 | |||||
chr2:173907114
|
T | A | 1 | a0001c0001t0073 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2827A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 2827 | chr2 | 173907114 | |||||
chr2:173907183
|
C | A | 15 | a0001c0001t0009a0001c0001t0010a0001c0001t0012others(12): Show | 38 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2758G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 2758 | chr2 | 173907183 | |||||
chr2:173907379
|
G | A | 2 | a0001c0001t0030a0001c0001t0031 | 4 | HG01255.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2562C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 2562 | chr2 | 173907379 | |||||
chr2:173907430
|
A | G | 5 | a0001c0001t0009a0001c0001t0018a0001c0001t0035others(2): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2511T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 2511 | chr2 | 173907430 | |||||
chr2:173907582
|
T | C | 13 | a0001c0001t0011a0001c0001t0022a0001c0001t0032others(10): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2359A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 2359 | chr2 | 173907582 | |||||
chr2:173907718
|
T | C | 3 | a0001c0001t0012a0001c0001t0033a0001c0001t0090 | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2223A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 2223 | chr2 | 173907718 | |||||
chr2:173907771
|
A | G | 1 | a0001c0001t0023 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2170T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 2170 | chr2 | 173907771 | |||||
chr2:173907932
|
G | A | 20 | a0001c0001t0005a0001c0001t0011a0001c0001t0022others(17): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2009C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 2009 | chr2 | 173907932 | |||||
chr2:173908113
|
C | CA | 8 | a0001c0001t0009a0001c0001t0012a0001c0001t0018others(5): Show | 25 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1827dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 1827 | chr2 | 173908113 | |||||
chr2:173908154
|
C | T | 1 | a0001c0001t0054 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1787G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 1787 | chr2 | 173908154 | |||||
chr2:173908182
|
A | C | 5 | a0001c0001t0009a0001c0001t0018a0001c0001t0035others(2): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1759T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 1759 | chr2 | 173908182 | |||||
chr2:173908200
|
C | T | 32 | a0001c0001t0003a0001c0001t0014a0001c0001t0015others(29): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1741G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 1741 | chr2 | 173908200 | |||||
chr2:173908234
|
G | A | 1 | a0001c0001t0091 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1707C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 1707 | chr2 | 173908234 | |||||
chr2:173908393
|
T | C | 2 | a0001c0001t0092a0001c0001t0093 | 2 | HG01070.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1548A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 1548 | chr2 | 173908393 | |||||
chr2:173908473
|
C | A | 1 | a0001c0001t0094 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1468G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 1468 | chr2 | 173908473 | |||||
chr2:173908910
|
CA | C | 5 | a0001c0001t0009a0001c0001t0018a0001c0001t0035others(2): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1030delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 1030 | chr2 | 173908910 | |||||
chr2:173909076
|
G | A | 1 | a0001c0001t0095 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 865 | chr2 | 173909076 | |||||
chr2:173909442
|
T | C | 1 | a0001c0001t0096 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*499A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 499 | chr2 | 173909442 | |||||
chr2:173909638
|
G | A | 1 | a0001c0001t0034 | 2 | HG00735.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*303C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 7/7 | 303 | chr2 | 173909638 | |||||
chr2:173965219
|
G | A | 2 | a0001c0005t0097a0001c0005t0098 | 2 | HG02895.hp2 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-48C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/7 | 48 | chr2 | 173965219 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:173910358
|
G | A | 1 | a0001c0001t0007g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2030-101C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173910358 | ||||||
chr2:173910369
|
G | C | 1 | a0001c0001t0016g0232 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2030-112C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173910369 | ||||||
chr2:173910389
|
C | A | 1 | a0001c0001t0071g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2030-132G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173910389 | ||||||
chr2:173910834
|
T | C | 233 | a0001c0001t0001g0146a0001c0001t0003g0220a0001c0001t0003g0233others(230): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.2030-577A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173910834 | ||||||
chr2:173910925
|
T | G | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.2030-668A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173910925 | ||||||
chr2:173910956
|
CCAA | C | 4 | a0001c0001t0015g0068a0001c0001t0015g0307a0001c0001t0015g0310others(1): Show | 4 | HG01346.hp1 HG01993.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.2030-702_2030-700d others(5): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173910956 | ||||||
chr2:173910959
|
A | G | 20 | a0001c0001t0015g0306a0001c0001t0015g0311a0001c0001t0015g0320others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.2030-702T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173910959 | ||||||
chr2:173910979
|
A | G | 1 | a0001c0001t0016g0228 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2030-722T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173910979 | ||||||
chr2:173911070
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2030-813A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911070 | ||||||
chr2:173911100
|
A | T | 1 | a0001c0001t0006g0110 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2030-843T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911100 | ||||||
chr2:173911224
|
T | G | 22 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.2030-967A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911224 | ||||||
chr2:173911264
|
AAC | A | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.2030-1009_2030-100 others(6): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911264 | ||||||
chr2:173911363
|
C | T | 19 | a0001c0001t0006g0110a0001c0001t0006g0111a0001c0001t0006g0112others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.2030-1106G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911363 | ||||||
chr2:173911368
|
C | T | 2 | a0001c0001t0007g0120a0001c0001t0007g0122 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2030-1111G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911368 | ||||||
chr2:173911398
|
C | T | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG02886.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2030-1141G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911398 | ||||||
chr2:173911435
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2030-1178G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911435 | ||||||
chr2:173911447
|
T | G | 1 | a0001c0001t0001g0329 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2030-1190A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911447 | ||||||
chr2:173911536
|
A | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2030-1279T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911536 | ||||||
chr2:173911684
|
A | G | 1 | a0001c0001t0006g0118 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2029+1386T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911684 | ||||||
chr2:173911758
|
T | C | 1 | a0002c0002t0002g0241 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2029+1312A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911758 | ||||||
chr2:173911813
|
C | CT | 14 | a0001c0001t0001g0153a0001c0001t0001g0157a0001c0001t0007g0327others(11): Show | 15 | HG01243.hp2 HG01515.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.2029+1256dupA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911813 | ||||||
chr2:173911813
|
C | CTTT | 38 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(35): Show | 38 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.2029+1254_2029+125 others(7): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911813 | ||||||
chr2:173911813
|
C | CTTTT | 6 | a0001c0001t0005g0028a0001c0001t0005g0038a0001c0001t0011g0043others(3): Show | 6 | HG01081.hp2 HG01106.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.2029+1253_2029+125 others(8): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911813 | ||||||
chr2:173911813
|
CT | C | 38 | a0001c0001t0001g0152a0001c0001t0003g0220a0001c0001t0003g0279others(35): Show | 38 | HG00621.hp1 HG01884.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.2029+1256delA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911813 | ||||||
chr2:173911813
|
CTT | C | 104 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0003g0233others(101): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.2029+1255_2029+125 others(6): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911813 | ||||||
chr2:173911813
|
CTTT | C | 19 | a0001c0001t0004g0138a0001c0001t0009g0001a0001c0001t0009g0081others(16): Show | 22 | HG00323.hp1 HG00735.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2029+1254_2029+125 others(7): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911813 | ||||||
chr2:173911874
|
A | G | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2029+1196T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911874 | ||||||
chr2:173911882
|
G | C | 2 | a0001c0001t0010g0096a0001c0001t0075g0288 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2029+1188C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911882 | ||||||
chr2:173911905
|
G | A | 11 | a0001c0001t0001g0146a0001c0001t0012g0292a0001c0001t0012g0293others(8): Show | 11 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.2029+1165C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911905 | ||||||
chr2:173911974
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2029+1096G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173911974 | ||||||
chr2:173912064
|
C | G | 20 | a0001c0001t0006g0107a0001c0001t0006g0110a0001c0001t0006g0111others(17): Show | 20 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.2029+1006G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173912064 | ||||||
chr2:173912320
|
T | C | 1 | a0001c0001t0004g0167 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2029+750A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173912320 | ||||||
chr2:173912397
|
C | G | 1 | a0001c0001t0001g0185 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2029+673G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173912397 | ||||||
chr2:173912417
|
G | T | 231 | a0001c0001t0001g0146a0001c0001t0003g0220a0001c0001t0003g0233others(228): Show | 238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.2029+653C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173912417 | ||||||
chr2:173912578
|
T | C | 1 | a0001c0001t0009g0084 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2029+492A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173912578 | ||||||
chr2:173912719
|
A | G | 1 | a0001c0001t0014g0325 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2029+351T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173912719 | ||||||
chr2:173912734
|
GA | G | 46 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(43): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.2029+335delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173912734 | ||||||
chr2:173912907
|
G | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2029+163C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173912907 | ||||||
chr2:173912919
|
T | C | 2 | a0001c0001t0007g0119a0001c0001t0059g0075 | 2 | NA19002.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2029+151A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173912919 | ||||||
chr2:173912971
|
ATC | A | 177 | a0001c0001t0001g0146a0001c0001t0003g0220a0001c0001t0003g0233others(174): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.2029+97_2029+98del others(2): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 6/6 | chr2 | 173912971 | ||||||
chr2:173913311
|
C | A | 1 | a0002c0002t0002g0212 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1833-45G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173913311 | ||||||
chr2:173913317
|
G | T | 1 | a0001c0001t0011g0052 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1833-51C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173913317 | ||||||
chr2:173913355
|
T | G | 1 | a0002c0002t0019g0073 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1833-89A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173913355 | ||||||
chr2:173913567
|
ATTC | A | 19 | a0001c0001t0006g0110a0001c0001t0006g0111a0001c0001t0006g0112others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1833-304_1833-302d others(5): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173913567 | ||||||
chr2:173913640
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1833-374C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173913640 | ||||||
chr2:173913699
|
G | A | 1 | a0001c0001t0068g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1833-433C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173913699 | ||||||
chr2:173913777
|
T | C | 1 | a0001c0001t0063g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1833-511A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173913777 | ||||||
chr2:173913800
|
T | C | 1 | a0002c0002t0002g0263 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1833-534A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173913800 | ||||||
chr2:173913812
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1833-546C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173913812 | ||||||
chr2:173913868
|
G | T | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1833-602C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173913868 | ||||||
chr2:173914034
|
G | C | 2 | a0001c0001t0011g0057a0001c0001t0086g0058 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1833-768C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173914034 | ||||||
chr2:173914040
|
G | A | 1 | a0002c0002t0002g0215 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1833-774C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173914040 | ||||||
chr2:173914059
|
G | C | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1833-793C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173914059 | ||||||
chr2:173914112
|
A | G | 1 | a0001c0001t0011g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1833-846T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173914112 | ||||||
chr2:173914171
|
TA | T | 223 | a0001c0001t0001g0146a0001c0001t0003g0220a0001c0001t0003g0233others(220): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1833-906delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173914171 | ||||||
chr2:173914262
|
C | T | 2 | a0001c0001t0006g0115a0001c0001t0006g0192 | 2 | NA18747.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1833-996G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173914262 | ||||||
chr2:173914584
|
G | A | 1 | a0001c0001t0010g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1833-1318C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173914584 | ||||||
chr2:173914723
|
C | T | 11 | a0001c0001t0001g0146a0001c0001t0012g0292a0001c0001t0012g0293others(8): Show | 11 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1833-1457G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173914723 | ||||||
chr2:173914813
|
C | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1833-1547G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173914813 | ||||||
chr2:173915082
|
T | A | 1 | a0001c0001t0065g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1833-1816A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173915082 | ||||||
chr2:173915104
|
G | A | 1 | a0001c0001t0005g0037 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1833-1838C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173915104 | ||||||
chr2:173915147
|
A | G | 1 | a0001c0001t0027g0160 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1833-1881T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173915147 | ||||||
chr2:173915148
|
G | A | 1 | a0001c0001t0027g0160 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1833-1882C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173915148 | ||||||
chr2:173915373
|
A | G | 1 | a0001c0001t0017g0172 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1833-2107T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173915373 | ||||||
chr2:173915478
|
T | C | 1 | a0001c0001t0032g0050 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1833-2212A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173915478 | ||||||
chr2:173915560
|
G | T | 1 | a0001c0001t0001g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1833-2294C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173915560 | ||||||
chr2:173915742
|
T | C | 3 | a0001c0001t0004g0138a0003c0003t0004g0069a0003c0003t0004g0315 | 3 | NA18965.hp2 NA18994.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1833-2476A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173915742 | ||||||
chr2:173916010
|
T | A | 1 | a0001c0001t0067g0199 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1832+2583A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916010 | ||||||
chr2:173916106
|
A | G | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1832+2487T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916106 | ||||||
chr2:173916290
|
A | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1832+2303T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916290 | ||||||
chr2:173916348
|
A | G | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1832+2245T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916348 | ||||||
chr2:173916425
|
C | T | 230 | a0001c0001t0001g0146a0001c0001t0003g0220a0001c0001t0003g0233others(227): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1832+2168G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916425 | ||||||
chr2:173916461
|
A | G | 1 | a0001c0001t0095g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1832+2132T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916461 | ||||||
chr2:173916496
|
G | C | 2 | a0001c0001t0006g0103a0001c0001t0006g0121 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1832+2097C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916496 | ||||||
chr2:173916557
|
C | T | 1 | a0002c0002t0002g0260 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1832+2036G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916557 | ||||||
chr2:173916565
|
T | C | 230 | a0001c0001t0001g0146a0001c0001t0003g0220a0001c0001t0003g0233others(227): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1832+2028A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916565 | ||||||
chr2:173916735
|
G | A | 5 | a0001c0001t0011g0052a0001c0001t0011g0055a0001c0001t0011g0056others(2): Show | 5 | HG00741.hp1 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1832+1858C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916735 | ||||||
chr2:173916861
|
C | T | 230 | a0001c0001t0001g0146a0001c0001t0003g0220a0001c0001t0003g0233others(227): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1832+1732G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916861 | ||||||
chr2:173916871
|
T | C | 2 | a0001c0001t0008g0094a0001c0001t0008g0095 | 2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1832+1722A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173916871 | ||||||
chr2:173917031
|
A | T | 230 | a0001c0001t0001g0146a0001c0001t0003g0220a0001c0001t0003g0233others(227): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1832+1562T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173917031 | ||||||
chr2:173917248
|
A | T | 32 | a0001c0001t0006g0103a0001c0001t0006g0110a0001c0001t0006g0111others(29): Show | 32 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1832+1345T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173917248 | ||||||
chr2:173917320
|
TTAAAC | T | 140 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(137): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1832+1268_1832+127 others(9): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173917320 | ||||||
chr2:173917371
|
A | C | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1832+1222T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173917371 | ||||||
chr2:173917392
|
G | A | 1 | a0001c0001t0027g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1832+1201C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173917392 | ||||||
chr2:173918001
|
T | A | 35 | a0001c0001t0001g0186a0001c0001t0003g0278a0001c0001t0006g0107others(32): Show | 35 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1832+592A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918001 | ||||||
chr2:173918001
|
T | TA | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1832+591dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918001 | ||||||
chr2:173918002
|
A | T | 1 | a0002c0002t0002g0258 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1832+591T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918002 | ||||||
chr2:173918124
|
T | TA | 5 | a0002c0002t0002g0070a0002c0002t0002g0210a0002c0002t0002g0250others(2): Show | 5 | NA18959.hp1 NA18973.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1832+468dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918124 | ||||||
chr2:173918146
|
A | G | 7 | a0001c0001t0005g0020a0001c0001t0005g0023a0001c0001t0005g0026others(4): Show | 7 | NA18947.hp1 NA18977.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1832+447T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918146 | ||||||
chr2:173918382
|
A | T | 1 | a0001c0001t0001g0149 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1832+211T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918382 | ||||||
chr2:173918397
|
T | C | 22 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1832+196A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918397 | ||||||
chr2:173918435
|
A | T | 2 | a0001c0001t0087g0044a0001c0001t0096g0301 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1832+158T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918435 | ||||||
chr2:173918464
|
CG | C | 19 | a0001c0001t0006g0110a0001c0001t0006g0111a0001c0001t0006g0112others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1832+128delC | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918464 | ||||||
chr2:173918510
|
T | A | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1832+83A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918510 | ||||||
chr2:173918519
|
T | C | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1832+74A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 5/6 | chr2 | 173918519 | ||||||
chr2:173918869
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1640-84T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173918869 | ||||||
chr2:173919023
|
T | C | 3 | a0001c0005t0074g0191a0001c0005t0097g0341a0001c0005t0098g0340 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1640-238A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919023 | ||||||
chr2:173919250
|
T | C | 1 | a0001c0001t0048g0202 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1640-465A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919250 | ||||||
chr2:173919303
|
C | T | 10 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(7): Show | 10 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-518G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919303 | ||||||
chr2:173919316
|
G | T | 1 | a0001c0001t0082g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1640-531C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919316 | ||||||
chr2:173919360
|
C | A | 2 | a0001c0001t0001g0064a0001c0001t0004g0174 | 2 | NA18975.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1640-575G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919360 | ||||||
chr2:173919566
|
AG | A | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-782delC | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919566 | ||||||
chr2:173919623
|
A | G | 1 | a0001c0001t0085g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1640-838T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919623 | ||||||
chr2:173919639
|
A | T | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-854T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919639 | ||||||
chr2:173919703
|
C | T | 22 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1640-918G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919703 | ||||||
chr2:173919710
|
A | C | 1 | a0001c0001t0010g0328 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1640-925T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919710 | ||||||
chr2:173919777
|
C | T | 24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 24 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1640-992G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919777 | ||||||
chr2:173919818
|
CTATA | C | 10 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(7): Show | 10 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-1037_1640-103 others(8): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919818 | ||||||
chr2:173919956
|
TC | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-1172delG | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173919956 | ||||||
chr2:173920042
|
T | C | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1640-1257A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920042 | ||||||
chr2:173920044
|
C | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-1259G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920044 | ||||||
chr2:173920084
|
G | GC | 24 | a0001c0001t0004g0174a0001c0001t0010g0096a0001c0001t0010g0098others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.1640-1300dupG | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920084 | ||||||
chr2:173920108
|
C | A | 2 | a0002c0002t0019g0253a0002c0002t0045g0254 | 2 | NA18972.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1640-1323G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920108 | ||||||
chr2:173920132
|
C | T | 2 | a0001c0001t0004g0060a0001c0001t0004g0132 | 2 | NA18947.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1640-1347G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920132 | ||||||
chr2:173920192
|
T | G | 24 | a0001c0001t0003g0282a0001c0001t0009g0001a0001c0001t0009g0081others(21): Show | 26 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1640-1407A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920192 | ||||||
chr2:173920474
|
G | A | 1 | a0001c0001t0085g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1640-1689C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920474 | ||||||
chr2:173920544
|
A | G | 142 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(139): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1640-1759T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920544 | ||||||
chr2:173920596
|
A | AATTT | 16 | a0001c0001t0008g0004a0001c0001t0008g0092a0001c0001t0010g0096others(13): Show | 17 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.1640-1815_1640-181 others(8): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920596 | ||||||
chr2:173920659
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1640-1874G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920659 | ||||||
chr2:173920682
|
C | T | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1640-1897G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920682 | ||||||
chr2:173920722
|
C | T | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-1937G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920722 | ||||||
chr2:173920739
|
C | T | 2 | a0001c0001t0007g0120a0001c0001t0007g0122 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1640-1954G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920739 | ||||||
chr2:173920749
|
C | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-1964G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920749 | ||||||
chr2:173920771
|
A | G | 1 | a0001c0001t0011g0043 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1640-1986T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920771 | ||||||
chr2:173920919
|
G | A | 1 | a0001c0001t0036g0324 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1640-2134C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173920919 | ||||||
chr2:173921026
|
T | G | 1 | a0001c0007t0008g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1640-2241A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921026 | ||||||
chr2:173921075
|
T | A | 1 | a0001c0001t0003g0272 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1640-2290A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921075 | ||||||
chr2:173921091
|
C | G | 230 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(227): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1640-2306G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921091 | ||||||
chr2:173921153
|
C | T | 2 | a0001c0001t0025g0012a0001c0001t0046g0287 | 3 | HG02258.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1640-2368G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921153 | ||||||
chr2:173921296
|
A | G | 1 | a0001c0001t0091g0337 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1640-2511T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921296 | ||||||
chr2:173921347
|
G | A | 2 | a0001c0001t0012g0299a0001c0001t0012g0300 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1640-2562C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921347 | ||||||
chr2:173921381
|
C | G | 2 | a0001c0001t0005g0035a0001c0001t0005g0036 | 2 | HG01106.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1640-2596G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921381 | ||||||
chr2:173921480
|
G | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-2695C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921480 | ||||||
chr2:173921530
|
A | AAAAC | 10 | a0001c0001t0001g0157a0001c0001t0001g0333a0001c0001t0004g0060others(7): Show | 10 | HG02056.hp2 NA18947.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-2749_1640-274 others(8): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921530 | ||||||
chr2:173921530
|
AAAAC | A | 230 | a0001c0001t0001g0126a0001c0001t0001g0146a0001c0001t0001g0193others(227): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1640-2749_1640-274 others(8): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921530 | ||||||
chr2:173921660
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0130a0001c0001t0004g0174 | 3 | NA18975.hp1 NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1640-2875C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921660 | ||||||
chr2:173921705
|
G | C | 1 | a0001c0001t0057g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1640-2920C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921705 | ||||||
chr2:173921796
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0326 | 2 | NA19078.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1640-3011A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921796 | ||||||
chr2:173921938
|
C | A | 1 | a0001c0001t0027g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1640-3153G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173921938 | ||||||
chr2:173922012
|
G | A | 2 | a0002c0002t0002g0011a0002c0002t0002g0217 | 3 | HG01256.hp1 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1640-3227C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922012 | ||||||
chr2:173922169
|
G | C | 1 | a0001c0001t0012g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1640-3384C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922169 | ||||||
chr2:173922248
|
T | C | 1 | a0001c0001t0016g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1640-3463A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922248 | ||||||
chr2:173922290
|
G | GT | 17 | a0001c0001t0001g0126a0001c0001t0009g0001a0001c0001t0009g0081others(14): Show | 19 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1640-3506dupA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922290 | ||||||
chr2:173922314
|
C | G | 1 | a0001c0001t0085g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1640-3529G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922314 | ||||||
chr2:173922502
|
C | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-3717G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922502 | ||||||
chr2:173922612
|
T | A | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-3827A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922612 | ||||||
chr2:173922640
|
G | A | 1 | a0001c0001t0078g0039 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1640-3855C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922640 | ||||||
chr2:173922768
|
C | A | 139 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(136): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1640-3983G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922768 | ||||||
chr2:173922896
|
AT | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0092a0001c0001t0026g0338others(2): Show | 6 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1640-4112delA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922896 | ||||||
chr2:173922979
|
A | G | 1 | a0001c0001t0056g0175 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1640-4194T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173922979 | ||||||
chr2:173923147
|
T | G | 2 | a0001c0001t0025g0012a0001c0001t0046g0287 | 3 | HG02258.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1640-4362A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173923147 | ||||||
chr2:173923287
|
T | A | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1640-4502A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173923287 | ||||||
chr2:173923721
|
T | G | 2 | a0001c0001t0006g0111a0001c0001t0006g0117 | 2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1640-4936A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173923721 | ||||||
chr2:173923757
|
ATTTGAT | A | 22 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1640-4978_1640-497 others(10): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173923757 | ||||||
chr2:173923866
|
A | G | 5 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01074.hp1 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640-5081T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173923866 | ||||||
chr2:173923977
|
A | G | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-5192T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173923977 | ||||||
chr2:173924047
|
G | A | 1 | a0001c0001t0006g0112 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1640-5262C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173924047 | ||||||
chr2:173924242
|
T | C | 11 | a0001c0001t0001g0146a0001c0001t0012g0292a0001c0001t0012g0293others(8): Show | 11 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1640-5457A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173924242 | ||||||
chr2:173924393
|
G | C | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1640-5608C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173924393 | ||||||
chr2:173924404
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1640-5619T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173924404 | ||||||
chr2:173924490
|
T | A | 1 | a0001c0001t0003g0272 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1640-5705A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173924490 | ||||||
chr2:173924545
|
G | T | 1 | a0001c0001t0068g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1640-5760C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173924545 | ||||||
chr2:173924600
|
T | C | 22 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1640-5815A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173924600 | ||||||
chr2:173924791
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-6006A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173924791 | ||||||
chr2:173924839
|
A | C | 1 | a0001c0001t0071g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1640-6054T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173924839 | ||||||
chr2:173924926
|
C | T | 5 | a0001c0001t0016g0228a0001c0001t0016g0232a0001c0001t0023g0226others(2): Show | 5 | HG00140.hp1 HG00323.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640-6141G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173924926 | ||||||
chr2:173925058
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1640-6273G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925058 | ||||||
chr2:173925078
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0137a0003c0003t0004g0313 | 3 | NA18954.hp2 NA19065.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1640-6293C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925078 | ||||||
chr2:173925178
|
G | A | 3 | a0001c0001t0006g0115a0001c0001t0006g0192a0001c0001t0014g0246 | 3 | HG03491.hp2 NA18747.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1640-6393C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925178 | ||||||
chr2:173925189
|
C | T | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-6404G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925189 | ||||||
chr2:173925222
|
T | C | 2 | a0001c0001t0025g0012a0001c0001t0046g0287 | 3 | HG02258.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1640-6437A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925222 | ||||||
chr2:173925268
|
T | G | 1 | a0001c0001t0048g0202 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1640-6483A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925268 | ||||||
chr2:173925403
|
T | C | 1 | a0001c0001t0060g0125 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1640-6618A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925403 | ||||||
chr2:173925453
|
G | C | 10 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(7): Show | 10 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-6668C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925453 | ||||||
chr2:173925567
|
T | C | 11 | a0001c0001t0001g0146a0001c0001t0012g0292a0001c0001t0012g0293others(8): Show | 11 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1640-6782A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925567 | ||||||
chr2:173925778
|
G | C | 1 | a0001c0001t0079g0019 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1640-6993C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925778 | ||||||
chr2:173925922
|
T | G | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-7137A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925922 | ||||||
chr2:173925954
|
C | T | 3 | a0001c0005t0074g0191a0001c0005t0097g0341a0001c0005t0098g0340 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1640-7169G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173925954 | ||||||
chr2:173926001
|
C | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-7216G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173926001 | ||||||
chr2:173926193
|
A | C | 19 | a0001c0001t0006g0110a0001c0001t0006g0111a0001c0001t0006g0112others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1640-7408T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173926193 | ||||||
chr2:173926256
|
A | T | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1640-7471T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173926256 | ||||||
chr2:173926545
|
T | C | 1 | a0001c0001t0086g0058 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1640-7760A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173926545 | ||||||
chr2:173926616
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1640-7831G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173926616 | ||||||
chr2:173926632
|
T | C | 1 | a0001c0001t0005g0016 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1640-7847A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173926632 | ||||||
chr2:173926699
|
T | A | 1 | a0001c0001t0001g0334 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1640-7914A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173926699 | ||||||
chr2:173926719
|
C | A | 2 | a0001c0001t0005g0016a0001c0001t0005g0017 | 2 | HG03654.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1640-7934G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173926719 | ||||||
chr2:173926820
|
T | C | 4 | a0001c0007t0008g0105a0001c0007t0008g0136a0002c0002t0002g0258others(1): Show | 4 | HG02630.hp1 HG03130.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1640-8035A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173926820 | ||||||
chr2:173926885
|
G | A | 2 | a0001c0001t0009g0085a0001c0001t0009g0087 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1640-8100C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173926885 | ||||||
chr2:173927022
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0326 | 2 | NA19078.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1640-8237A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927022 | ||||||
chr2:173927075
|
G | A | 6 | a0002c0002t0002g0011a0002c0002t0002g0065a0002c0002t0002g0217others(3): Show | 7 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1640-8290C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927075 | ||||||
chr2:173927112
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1640-8327G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927112 | ||||||
chr2:173927126
|
C | A | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-8341G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927126 | ||||||
chr2:173927162
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1640-8377A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927162 | ||||||
chr2:173927197
|
C | G | 1 | a0001c0001t0014g0245 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1640-8412G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927197 | ||||||
chr2:173927211
|
C | A | 2 | a0001c0001t0010g0099a0001c0001t0010g0312 | 2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1640-8426G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927211 | ||||||
chr2:173927228
|
T | C | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1640-8443A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927228 | ||||||
chr2:173927272
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0071g0102 | 2 | HG02258.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1640-8487T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927272 | ||||||
chr2:173927276
|
CT | C | 27 | a0001c0001t0001g0129a0001c0001t0005g0031a0001c0001t0008g0004others(24): Show | 30 | HG00099.hp1 HG00735.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1640-8492delA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927276 | ||||||
chr2:173927402
|
G | A | 1 | a0001c0001t0085g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1640-8617C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927402 | ||||||
chr2:173927421
|
T | C | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1640-8636A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927421 | ||||||
chr2:173927426
|
G | A | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-8641C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927426 | ||||||
chr2:173927438
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1640-8653C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927438 | ||||||
chr2:173927498
|
G | A | 11 | a0001c0001t0001g0146a0001c0001t0012g0292a0001c0001t0012g0293others(8): Show | 11 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1640-8713C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927498 | ||||||
chr2:173927746
|
T | C | 22 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1640-8961A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927746 | ||||||
chr2:173927830
|
C | G | 1 | a0001c0001t0035g0088 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1640-9045G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927830 | ||||||
chr2:173927966
|
T | G | 5 | a0001c0001t0017g0006a0001c0001t0017g0164a0001c0001t0017g0172others(2): Show | 6 | HG01934.hp2 HG01943.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1640-9181A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927966 | ||||||
chr2:173927989
|
T | C | 1 | a0002c0002t0044g0239 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1640-9204A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173927989 | ||||||
chr2:173928041
|
A | G | 110 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(107): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1640-9256T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928041 | ||||||
chr2:173928239
|
G | A | 1 | a0001c0001t0032g0014 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1640-9454C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928239 | ||||||
chr2:173928343
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1640-9558C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928343 | ||||||
chr2:173928503
|
T | TA | 7 | a0001c0001t0001g0142a0001c0001t0016g0225a0001c0001t0040g0222others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1640-9719dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928503 | ||||||
chr2:173928503
|
TA | T | 34 | a0001c0001t0001g0153a0001c0001t0006g0103a0001c0001t0006g0107others(31): Show | 34 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1640-9719delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928503 | ||||||
chr2:173928575
|
AATCCTGA others(6): Show |
A | 11 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(8): Show | 11 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1640-9803_1640-979 others(17): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928575 | ||||||
chr2:173928594
|
T | TA | 11 | a0001c0001t0001g0146a0001c0001t0012g0292a0001c0001t0012g0293others(8): Show | 11 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1640-9810dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928594 | ||||||
chr2:173928759
|
T | C | 1 | a0001c0001t0003g0276 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1640-9974A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928759 | ||||||
chr2:173928843
|
A | G | 24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 24 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1640-10058T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928843 | ||||||
chr2:173928884
|
T | C | 12 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1640-10099A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928884 | ||||||
chr2:173928889
|
C | T | 1 | a0002c0002t0002g0286 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1640-10104G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928889 | ||||||
chr2:173928914
|
A | G | 1 | a0001c0001t0036g0324 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1640-10129T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173928914 | ||||||
chr2:173929150
|
C | T | 4 | a0002c0002t0002g0205a0002c0002t0002g0216a0002c0002t0013g0267others(1): Show | 4 | NA18977.hp1 NA18978.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1640-10365G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929150 | ||||||
chr2:173929163
|
A | G | 1 | a0001c0001t0095g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1640-10378T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929163 | ||||||
chr2:173929169
|
T | C | 23 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(20): Show | 25 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1640-10384A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929169 | ||||||
chr2:173929212
|
G | A | 146 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(143): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1640-10427C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929212 | ||||||
chr2:173929473
|
A | T | 1 | a0001c0001t0010g0328 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1640-10688T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929473 | ||||||
chr2:173929478
|
A | G | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1640-10693T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929478 | ||||||
chr2:173929562
|
A | T | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1640-10777T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929562 | ||||||
chr2:173929603
|
T | C | 2 | a0001c0001t0014g0245a0001c0001t0024g0207 | 2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1640-10818A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929603 | ||||||
chr2:173929818
|
T | C | 2 | a0001c0001t0025g0012a0001c0001t0046g0287 | 3 | HG02258.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1640-11033A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929818 | ||||||
chr2:173929819
|
G | A | 110 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(107): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1640-11034C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929819 | ||||||
chr2:173929847
|
A | G | 2 | a0001c0001t0007g0134a0001c0001t0007g0135 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1640-11062T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929847 | ||||||
chr2:173929898
|
T | C | 1 | a0001c0001t0077g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1640-11113A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929898 | ||||||
chr2:173929903
|
G | A | 1 | a0001c0001t0010g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1640-11118C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929903 | ||||||
chr2:173929920
|
C | G | 45 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(42): Show | 45 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.1640-11135G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929920 | ||||||
chr2:173929920
|
C | T | 1 | a0001c0001t0076g0097 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1640-11135G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173929920 | ||||||
chr2:173930042
|
T | C | 12 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1640-11257A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173930042 | ||||||
chr2:173930242
|
A | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-11457T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173930242 | ||||||
chr2:173930317
|
A | G | 5 | a0001c0001t0008g0004a0001c0001t0008g0092a0001c0001t0026g0338others(2): Show | 6 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1640-11532T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173930317 | ||||||
chr2:173930353
|
G | A | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1640-11568C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173930353 | ||||||
chr2:173930414
|
G | GA | 8 | a0001c0001t0001g0152a0001c0001t0009g0001a0001c0001t0009g0081others(5): Show | 10 | HG01257.hp1 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1640-11630dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173930414 | ||||||
chr2:173930553
|
A | G | 2 | a0001c0004t0007g0318a0001c0004t0007g0319 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1640-11768T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173930553 | ||||||
chr2:173930635
|
C | T | 5 | a0002c0002t0019g0073a0002c0002t0019g0237a0002c0002t0019g0253others(2): Show | 5 | NA18939.hp2 NA18972.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1640-11850G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173930635 | ||||||
chr2:173930648
|
G | A | 12 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1640-11863C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173930648 | ||||||
chr2:173930651
|
C | T | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-11866G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173930651 | ||||||
chr2:173930773
|
T | A | 12 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1640-11988A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173930773 | ||||||
chr2:173931091
|
A | T | 1 | a0001c0001t0029g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1640-12306T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931091 | ||||||
chr2:173931113
|
C | T | 24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 24 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1640-12328G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931113 | ||||||
chr2:173931122
|
A | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-12337T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931122 | ||||||
chr2:173931142
|
A | T | 2 | a0001c0001t0011g0057a0001c0001t0086g0058 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1640-12357T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931142 | ||||||
chr2:173931214
|
A | G | 23 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(20): Show | 25 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1640-12429T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931214 | ||||||
chr2:173931344
|
T | TTTGTTGT others(2): Show |
12 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1640-12560_1640-12 others(15): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931344 | ||||||
chr2:173931344
|
T | TTTGTTGT others(2): Show |
109 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(106): Show | 112 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(109): Show |
intron_variant | MODIFIER | c.1640-12568_1640-12 others(15): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931344 | ||||||
chr2:173931344
|
TTTG | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0001g0144 | 3 | HG02027.hp1 HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1640-12562_1640-12 others(9): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931344 | ||||||
chr2:173931393
|
G | A | 12 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1640-12608C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931393 | ||||||
chr2:173931436
|
C | A | 1 | a0001c0001t0010g0101 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1640-12651G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931436 | ||||||
chr2:173931477
|
A | G | 23 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(20): Show | 25 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1640-12692T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931477 | ||||||
chr2:173931553
|
A | AGGCTGG | 112 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(109): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.1640-12774_1640-12 others(12): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931553 | ||||||
chr2:173931571
|
T | G | 1 | a0001c0001t0022g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1640-12786A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931571 | ||||||
chr2:173931622
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1640-12837C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931622 | ||||||
chr2:173931691
|
C | G | 22 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1640-12906G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931691 | ||||||
chr2:173931761
|
C | G | 4 | a0001c0004t0007g0316a0001c0004t0007g0317a0001c0004t0007g0318others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1640-12976G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931761 | ||||||
chr2:173931764
|
T | C | 12 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1640-12979A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931764 | ||||||
chr2:173931954
|
C | T | 1 | a0001c0001t0054g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1640-13169G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931954 | ||||||
chr2:173931960
|
T | C | 4 | a0002c0002t0002g0205a0002c0002t0002g0216a0002c0002t0013g0267others(1): Show | 4 | NA18977.hp1 NA18978.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1640-13175A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173931960 | ||||||
chr2:173932169
|
T | A | 1 | a0001c0001t0057g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1640-13384A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173932169 | ||||||
chr2:173932180
|
T | C | 9 | a0001c0001t0022g0046a0001c0001t0022g0047a0001c0001t0022g0049others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1640-13395A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173932180 | ||||||
chr2:173932238
|
C | T | 1 | a0001c0001t0012g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1640-13453G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173932238 | ||||||
chr2:173932303
|
T | A | 110 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(107): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1640-13518A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173932303 | ||||||
chr2:173932352
|
C | T | 1 | a0001c0001t0068g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1640-13567G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173932352 | ||||||
chr2:173932364
|
G | A | 5 | a0001c0001t0012g0292a0001c0001t0012g0297a0001c0001t0012g0298others(2): Show | 5 | HG01261.hp1 HG01346.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640-13579C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173932364 | ||||||
chr2:173932537
|
G | A | 22 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1640-13752C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173932537 | ||||||
chr2:173932638
|
C | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG00438.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.1640-13853G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173932638 | ||||||
chr2:173932774
|
C | T | 2 | a0001c0001t0007g0120a0001c0001t0007g0122 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1640-13989G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173932774 | ||||||
chr2:173932853
|
T | G | 69 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(66): Show | 71 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1640-14068A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173932853 | ||||||
chr2:173933002
|
T | C | 2 | a0001c0004t0007g0318a0001c0004t0007g0319 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1640-14217A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933002 | ||||||
chr2:173933242
|
TG | T | 145 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(142): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1640-14458delC | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933242 | ||||||
chr2:173933264
|
A | G | 1 | a0001c0001t0003g0244 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1640-14479T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933264 | ||||||
chr2:173933336
|
G | A | 20 | a0001c0001t0006g0107a0001c0001t0006g0110a0001c0001t0006g0111others(17): Show | 20 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.1640-14551C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933336 | ||||||
chr2:173933348
|
G | A | 12 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1640-14563C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933348 | ||||||
chr2:173933408
|
C | G | 111 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(108): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1640-14623G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933408 | ||||||
chr2:173933555
|
T | C | 2 | a0001c0001t0012g0295a0001c0001t0090g0296 | 2 | HG00438.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1640-14770A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933555 | ||||||
chr2:173933638
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1640-14853A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTA | 48 | a0001c0001t0001g0007a0001c0001t0001g0127a0001c0001t0001g0141others(45): Show | 50 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1640-14855_1640-14 others(8): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATA | 27 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0151others(24): Show | 27 | HG00621.hp2 HG00639.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1640-14857_1640-14 others(10): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATA | 20 | a0001c0001t0001g0145a0001c0001t0005g0026a0001c0001t0006g0115others(17): Show | 20 | HG00140.hp2 HG00408.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1640-14859_1640-14 others(12): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(1): Show |
18 | a0001c0001t0004g0154a0001c0001t0015g0306a0001c0001t0015g0311others(15): Show | 18 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1640-14861_1640-14 others(14): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(3): Show |
18 | a0001c0001t0001g0146a0001c0001t0001g0155a0001c0001t0011g0043others(15): Show | 18 | HG00099.hp1 HG00642.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1640-14863_1640-14 others(16): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(5): Show |
14 | a0001c0001t0001g0156a0001c0001t0003g0233a0001c0001t0003g0282others(11): Show | 15 | HG01074.hp2 HG01515.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.1640-14865_1640-14 others(18): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(7): Show |
19 | a0001c0001t0003g0271a0001c0001t0003g0276a0001c0001t0004g0150others(16): Show | 20 | HG00323.hp1 HG01099.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1640-14867_1640-14 others(20): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(9): Show |
18 | a0001c0001t0003g0234a0001c0001t0003g0270a0001c0001t0003g0277others(15): Show | 20 | HG00735.hp1 HG01255.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.1640-14869_1640-14 others(22): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(11): Show |
18 | a0001c0001t0003g0278a0001c0001t0005g0027a0001c0001t0005g0028others(15): Show | 18 | HG00140.hp1 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1640-14871_1640-14 others(24): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(13): Show |
11 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0005g0017others(8): Show | 11 | HG02145.hp1 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1640-14873_1640-14 others(26): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(15): Show |
6 | a0001c0001t0001g0330a0001c0001t0003g0273a0001c0001t0005g0030others(3): Show | 6 | HG02080.hp2 HG02976.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.1640-14875_1640-14 others(28): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(17): Show |
2 | a0001c0001t0005g0023a0001c0001t0034g0022 | 2 | HG02818.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1640-14877_1640-14 others(30): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(21): Show |
1 | a0001c0001t0015g0307 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1640-14881_1640-14 others(34): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0011g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1640-14883_1640-14 others(36): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
TTA | T | 19 | a0001c0001t0001g0152a0001c0001t0001g0194a0001c0001t0001g0198others(16): Show | 19 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.1640-14855_1640-14 others(8): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
TTATA | T | 8 | a0001c0001t0001g0106a0001c0001t0007g0120a0001c0001t0007g0122others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1640-14857_1640-14 others(10): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
TTATATAT others(1): Show |
T | 8 | a0001c0001t0001g0302a0001c0001t0026g0338a0001c0001t0026g0339others(5): Show | 8 | HG02486.hp1 HG02970.hp1 NA18522.hp2 others(5): Show |
intron_variant | MODIFIER | c.1640-14861_1640-14 others(14): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
TTATATAT others(3): Show |
T | 2 | a0001c0001t0008g0004a0001c0001t0008g0092 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1640-14863_1640-14 others(16): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933638
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0015g0310 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1640-14873_1640-14 others(26): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933638 | ||||||
chr2:173933639
|
T | C | 1 | a0001c0001t0062g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1640-14854A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933639 | ||||||
chr2:173933641
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1640-14856A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933641 | ||||||
chr2:173933645
|
T | C | 8 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(5): Show | 10 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1640-14860A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933645 | ||||||
chr2:173933647
|
T | C | 3 | a0001c0001t0009g0084a0001c0001t0018g0321a0001c0001t0037g0083 | 3 | HG01928.hp1 HG02300.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1640-14862A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933647 | ||||||
chr2:173933671
|
T | TATATATA others(5): Show |
1 | a0001c0001t0038g0290 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1640-14887_1640-14 others(18): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933671 | ||||||
chr2:173933673
|
A | T | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1640-14888T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933673 | ||||||
chr2:173933736
|
C | A | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1640-14951G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933736 | ||||||
chr2:173933740
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | NA18974.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1640-14955G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933740 | ||||||
chr2:173933767
|
C | G | 69 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(66): Show | 71 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1640-14982G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933767 | ||||||
chr2:173933990
|
T | TG | 333 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(330): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1640-15206dupC | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173933990 | ||||||
chr2:173934003
|
G | A | 46 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(43): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1640-15218C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934003 | ||||||
chr2:173934010
|
T | C | 9 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0004g0167others(6): Show | 10 | HG00544.hp1 HG01934.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-15225A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934010 | ||||||
chr2:173934132
|
C | T | 108 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(105): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1640-15347G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934132 | ||||||
chr2:173934236
|
T | TA | 11 | a0001c0001t0007g0133a0001c0001t0012g0292a0001c0001t0012g0293others(8): Show | 11 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1640-15452dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934236 | ||||||
chr2:173934291
|
T | C | 1 | a0001c0001t0014g0067 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1640-15506A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934291 | ||||||
chr2:173934312
|
AT | A | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-15528delA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934312 | ||||||
chr2:173934408
|
T | C | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-15623A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934408 | ||||||
chr2:173934418
|
G | T | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-15633C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934418 | ||||||
chr2:173934442
|
C | A | 56 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(53): Show | 56 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1640-15657G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934442 | ||||||
chr2:173934444
|
A | G | 9 | a0002c0002t0002g0208a0002c0002t0002g0214a0002c0002t0002g0238others(6): Show | 9 | HG02027.hp2 HG02074.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1640-15659T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934444 | ||||||
chr2:173934480
|
A | G | 1 | a0001c0001t0011g0043 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1640-15695T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934480 | ||||||
chr2:173934501
|
A | T | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1640-15716T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934501 | ||||||
chr2:173934673
|
A | G | 11 | a0001c0001t0006g0103a0001c0001t0006g0121a0001c0001t0007g0120others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1640-15888T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173934673 | ||||||
chr2:173935058
|
A | T | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1640-16273T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173935058 | ||||||
chr2:173935296
|
A | G | 9 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(6): Show | 9 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1640-16511T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173935296 | ||||||
chr2:173935471
|
G | C | 2 | a0001c0005t0097g0341a0001c0005t0098g0340 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1640-16686C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173935471 | ||||||
chr2:173935854
|
A | ACAACGGA others(31): Show |
10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-17107_1640-17 others(44): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173935854 | ||||||
chr2:173935854
|
ACAACGGA others(31): Show |
A | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1640-17107_1640-17 others(44): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173935854 | ||||||
chr2:173935896
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1640-17111G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173935896 | ||||||
chr2:173935939
|
T | C | 1 | a0001c0001t0091g0337 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1640-17154A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173935939 | ||||||
chr2:173935947
|
A | G | 10 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(7): Show | 10 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-17162T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173935947 | ||||||
chr2:173935950
|
C | T | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 242 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.1640-17165G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173935950 | ||||||
chr2:173936110
|
C | T | 3 | a0001c0005t0074g0191a0001c0005t0097g0341a0001c0005t0098g0340 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1640-17325G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173936110 | ||||||
chr2:173936801
|
CT | C | 50 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(47): Show | 50 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.1640-18017delA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173936801 | ||||||
chr2:173936961
|
C | G | 5 | a0001c0001t0011g0052a0001c0001t0011g0055a0001c0001t0011g0056others(2): Show | 5 | HG00741.hp1 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1639+17912G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173936961 | ||||||
chr2:173937134
|
T | A | 59 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(56): Show | 61 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1639+17739A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937134 | ||||||
chr2:173937222
|
G | C | 1 | a0002c0002t0002g0238 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1639+17651C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937222 | ||||||
chr2:173937272
|
T | C | 32 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(29): Show | 32 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1639+17601A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937272 | ||||||
chr2:173937462
|
C | G | 9 | a0002c0002t0002g0208a0002c0002t0002g0214a0002c0002t0002g0238others(6): Show | 9 | HG02027.hp2 HG02074.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1639+17411G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937462 | ||||||
chr2:173937509
|
C | T | 1 | a0001c0001t0077g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1639+17364G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937509 | ||||||
chr2:173937568
|
T | C | 46 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(43): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1639+17305A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937568 | ||||||
chr2:173937656
|
A | T | 1 | a0001c0001t0017g0172 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1639+17217T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937656 | ||||||
chr2:173937694
|
A | T | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1639+17179T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937694 | ||||||
chr2:173937846
|
C | A | 2 | a0001c0001t0033g0066a0001c0001t0033g0294 | 2 | NA18950.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1639+17027G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937846 | ||||||
chr2:173937851
|
T | C | 1 | a0001c0001t0035g0088 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1639+17022A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937851 | ||||||
chr2:173937959
|
G | A | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1639+16914C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937959 | ||||||
chr2:173937984
|
G | A | 1 | a0002c0002t0002g0286 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1639+16889C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173937984 | ||||||
chr2:173938013
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1639+16860A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173938013 | ||||||
chr2:173938149
|
T | C | 39 | a0001c0001t0001g0076a0001c0001t0001g0126a0001c0001t0001g0127others(36): Show | 39 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1639+16724A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173938149 | ||||||
chr2:173938248
|
G | A | 46 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(43): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1639+16625C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173938248 | ||||||
chr2:173938373
|
C | T | 1 | a0001c0001t0016g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1639+16500G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173938373 | ||||||
chr2:173938459
|
C | CA | 69 | a0001c0001t0001g0013a0001c0001t0001g0076a0001c0001t0001g0149others(66): Show | 71 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.1639+16413dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173938459 | ||||||
chr2:173938459
|
C | CAAAAA | 7 | a0001c0001t0009g0001a0001c0001t0009g0082a0001c0001t0009g0084others(4): Show | 9 | HG01257.hp1 HG01258.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1639+16409_1639+16 others(11): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173938459 | ||||||
chr2:173938459
|
CA | C | 15 | a0001c0001t0003g0271a0001c0001t0005g0016a0001c0001t0005g0017others(12): Show | 16 | HG00597.hp2 HG00639.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1639+16413delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173938459 | ||||||
chr2:173938587
|
G | T | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1639+16286C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173938587 | ||||||
chr2:173938765
|
A | G | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1639+16108T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173938765 | ||||||
chr2:173938986
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(107): Show | 118 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1639+15887A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173938986 | ||||||
chr2:173939092
|
A | T | 4 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0200others(1): Show | 4 | HG00738.hp2 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639+15781T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939092 | ||||||
chr2:173939152
|
A | G | 1 | a0001c0001t0005g0024 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1639+15721T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939152 | ||||||
chr2:173939203
|
C | G | 1 | a0001c0001t0021g0221 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1639+15670G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939203 | ||||||
chr2:173939377
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1639+15496C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939377 | ||||||
chr2:173939461
|
T | C | 5 | a0002c0002t0002g0011a0002c0002t0002g0217a0002c0002t0013g0218others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639+15412A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939461 | ||||||
chr2:173939492
|
G | A | 1 | a0001c0001t0021g0059 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1639+15381C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939492 | ||||||
chr2:173939501
|
T | C | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+15372A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939501 | ||||||
chr2:173939536
|
G | A | 24 | a0001c0001t0015g0068a0001c0001t0015g0306a0001c0001t0015g0307others(21): Show | 24 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1639+15337C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939536 | ||||||
chr2:173939563
|
A | G | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1639+15310T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939563 | ||||||
chr2:173939620
|
C | T | 1 | a0001c0001t0009g0084 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1639+15253G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939620 | ||||||
chr2:173939647
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1639+15226G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939647 | ||||||
chr2:173939740
|
G | A | 24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 24 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1639+15133C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939740 | ||||||
chr2:173939764
|
C | CAAAAA | 9 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(6): Show | 9 | HG02572.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1639+15104_1639+15 others(11): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(1): Show |
11 | a0001c0001t0009g0001a0001c0001t0009g0082a0001c0001t0009g0084others(8): Show | 13 | HG01257.hp1 HG01258.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1639+15101_1639+15 others(14): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(2): Show |
23 | a0001c0001t0007g0327a0001c0001t0009g0081a0001c0001t0011g0043others(20): Show | 23 | HG00735.hp2 HG00741.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1639+15100_1639+15 others(15): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(3): Show |
24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 25 | HG00735.hp1 HG01081.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1639+15099_1639+15 others(16): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(4): Show |
23 | a0001c0001t0001g0130a0001c0001t0001g0157a0001c0001t0001g0169others(20): Show | 23 | HG00438.hp2 HG00621.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1639+15098_1639+15 others(17): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(5): Show |
52 | a0001c0001t0001g0064a0001c0001t0001g0126a0001c0001t0001g0137others(49): Show | 55 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1639+15097_1639+15 others(18): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(6): Show |
39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(36): Show | 44 | HG00323.hp2 HG00609.hp2 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.1639+15096_1639+15 others(19): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(7): Show |
15 | a0001c0001t0001g0106a0001c0001t0001g0147a0001c0001t0001g0148others(12): Show | 15 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+15095_1639+15 others(20): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0155a0001c0001t0006g0111a0001c0001t0006g0117others(3): Show | 6 | HG01074.hp1 HG03098.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639+15094_1639+15 others(21): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0156a0001c0001t0001g0195 | 2 | HG00438.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1639+15093_1639+15 others(22): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0007g0120 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1639+15092_1639+15 others(23): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0006g0103a0001c0001t0006g0121a0001c0001t0007g0122 | 3 | HG01891.hp2 HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1639+15091_1639+15 others(24): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(12): Show |
6 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0007g0134others(3): Show | 6 | HG01071.hp2 HG01167.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639+15108_1639+15 others(25): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0007g0133a0001c0004t0007g0317 | 2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1639+15108_1639+15 others(26): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0007g0135a0001c0001t0007g0139 | 2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1639+15108_1639+15 others(27): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0006g0192 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1639+15108_1639+15 others(28): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0006g0115a0001c0001t0006g0118 | 2 | HG02698.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1639+15108_1639+15 others(29): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0072g0116 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1639+15108_1639+15 others(30): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(21): Show |
2 | a0001c0001t0006g0107a0001c0001t0007g0090 | 2 | HG01515.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1639+15108_1639+15 others(34): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0006g0110 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1639+15108_1639+15 others(41): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
C | CAAAAAAA others(35): Show |
1 | a0001c0001t0006g0113 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1639+15108_1639+15 others(48): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939764
|
CA | C | 92 | a0001c0001t0003g0244a0001c0001t0003g0273a0001c0001t0005g0037others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.1639+15108delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939764 | ||||||
chr2:173939788
|
A | T | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1639+15085T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939788 | ||||||
chr2:173939793
|
T | C | 7 | a0002c0002t0002g0262a0002c0002t0019g0073a0002c0002t0019g0237others(4): Show | 7 | HG02523.hp1 NA18939.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639+15080A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939793 | ||||||
chr2:173939838
|
T | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(197): Show | 211 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1639+15035A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939838 | ||||||
chr2:173939875
|
G | A | 9 | a0001c0001t0022g0046a0001c0001t0022g0047a0001c0001t0022g0049others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1639+14998C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939875 | ||||||
chr2:173939927
|
C | T | 3 | a0001c0001t0026g0338a0001c0001t0026g0339a0001c0001t0055g0091 | 3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1639+14946G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939927 | ||||||
chr2:173939991
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG00438.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.1639+14882C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173939991 | ||||||
chr2:173940017
|
G | A | 23 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(20): Show | 23 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1639+14856C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940017 | ||||||
chr2:173940042
|
T | G | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+14831A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940042 | ||||||
chr2:173940063
|
G | A | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+14810C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940063 | ||||||
chr2:173940074
|
G | C | 1 | a0001c0001t0054g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1639+14799C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940074 | ||||||
chr2:173940102
|
C | T | 1 | a0002c0002t0002g0284 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1639+14771G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940102 | ||||||
chr2:173940266
|
G | T | 1 | a0001c0001t0010g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1639+14607C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940266 | ||||||
chr2:173940290
|
T | C | 1 | a0001c0001t0022g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1639+14583A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940290 | ||||||
chr2:173940303
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1639+14570C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940303 | ||||||
chr2:173940375
|
T | C | 1 | a0001c0001t0071g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1639+14498A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940375 | ||||||
chr2:173940432
|
C | T | 2 | a0001c0001t0025g0012a0001c0001t0046g0287 | 3 | HG02258.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1639+14441G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940432 | ||||||
chr2:173940493
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(197): Show | 211 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1639+14380T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940493 | ||||||
chr2:173940537
|
T | G | 1 | a0001c0001t0006g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1639+14336A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940537 | ||||||
chr2:173940623
|
T | C | 2 | a0001c0001t0004g0077a0001c0001t0004g0150 | 2 | NA18962.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1639+14250A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940623 | ||||||
chr2:173940808
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1639+14065A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940808 | ||||||
chr2:173940886
|
G | C | 1 | a0001c0001t0007g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1639+13987C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940886 | ||||||
chr2:173940904
|
C | T | 1 | a0001c0007t0008g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1639+13969G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173940904 | ||||||
chr2:173941127
|
T | TA | 12 | a0001c0001t0001g0126a0001c0001t0004g0060a0001c0001t0004g0132others(9): Show | 13 | HG00099.hp1 HG02523.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1639+13745dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173941127 | ||||||
chr2:173941127
|
TA | T | 20 | a0001c0001t0001g0129a0001c0001t0005g0038a0001c0001t0006g0111others(17): Show | 22 | HG00735.hp2 HG01070.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.1639+13745delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173941127 | ||||||
chr2:173941127
|
TAA | T | 21 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(18): Show | 21 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1639+13744_1639+13 others(8): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173941127 | ||||||
chr2:173941239
|
A | G | 6 | a0002c0002t0002g0011a0002c0002t0002g0065a0002c0002t0002g0217others(3): Show | 7 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639+13634T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173941239 | ||||||
chr2:173941274
|
A | G | 22 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1639+13599T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173941274 | ||||||
chr2:173941389
|
C | G | 24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 24 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1639+13484G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173941389 | ||||||
chr2:173941408
|
G | C | 3 | a0001c0001t0001g0126a0001c0001t0001g0193a0001c0001t0001g0326 | 3 | NA18955.hp1 NA19078.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1639+13465C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173941408 | ||||||
chr2:173941452
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(107): Show | 118 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1639+13421A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173941452 | ||||||
chr2:173941699
|
T | A | 1 | a0001c0001t0031g0008 | 2 | HG01255.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1639+13174A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173941699 | ||||||
chr2:173941979
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+12894A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173941979 | ||||||
chr2:173942031
|
C | T | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+12842G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942031 | ||||||
chr2:173942039
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1639+12834C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942039 | ||||||
chr2:173942090
|
T | C | 1 | a0001c0001t0082g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1639+12783A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942090 | ||||||
chr2:173942124
|
G | A | 1 | a0001c0001t0006g0118 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1639+12749C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942124 | ||||||
chr2:173942395
|
A | T | 1 | a0002c0002t0013g0206 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1639+12478T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942395 | ||||||
chr2:173942396
|
T | C | 1 | a0002c0002t0013g0206 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1639+12477A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942396 | ||||||
chr2:173942481
|
G | A | 1 | a0003c0003t0004g0315 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1639+12392C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942481 | ||||||
chr2:173942540
|
T | C | 5 | a0001c0001t0008g0004a0001c0001t0008g0092a0001c0001t0026g0338others(2): Show | 6 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639+12333A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942540 | ||||||
chr2:173942580
|
G | A | 12 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1639+12293C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942580 | ||||||
chr2:173942686
|
C | A | 1 | a0001c0001t0003g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1639+12187G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942686 | ||||||
chr2:173942761
|
T | C | 8 | a0001c0001t0011g0043a0001c0001t0011g0052a0001c0001t0011g0053others(5): Show | 8 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1639+12112A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942761 | ||||||
chr2:173942763
|
C | T | 1 | a0001c0001t0005g0025 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1639+12110G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942763 | ||||||
chr2:173942767
|
A | G | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1639+12106T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942767 | ||||||
chr2:173942823
|
A | G | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+12050T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942823 | ||||||
chr2:173942887
|
T | C | 59 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(56): Show | 61 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1639+11986A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942887 | ||||||
chr2:173942917
|
A | G | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+11956T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942917 | ||||||
chr2:173942937
|
G | A | 9 | a0001c0001t0022g0046a0001c0001t0022g0047a0001c0001t0022g0049others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1639+11936C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942937 | ||||||
chr2:173942938
|
G | A | 6 | a0002c0002t0002g0011a0002c0002t0002g0065a0002c0002t0002g0217others(3): Show | 7 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639+11935C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173942938 | ||||||
chr2:173943002
|
T | C | 1 | a0001c0001t0010g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1639+11871A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173943002 | ||||||
chr2:173943480
|
C | T | 1 | a0001c0001t0010g0096 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1639+11393G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173943480 | ||||||
chr2:173943488
|
C | T | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1639+11385G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173943488 | ||||||
chr2:173943583
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0084g0041a0001c0001t0088g0051 | 3 | HG00741.hp1 HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1639+11290C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173943583 | ||||||
chr2:173943604
|
T | C | 3 | a0001c0005t0074g0191a0001c0005t0097g0341a0001c0005t0098g0340 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1639+11269A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173943604 | ||||||
chr2:173943611
|
A | G | 82 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(79): Show | 84 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.1639+11262T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173943611 | ||||||
chr2:173943629
|
C | T | 2 | a0001c0001t0008g0094a0001c0001t0008g0095 | 2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1639+11244G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173943629 | ||||||
chr2:173944059
|
C | G | 5 | a0001c0001t0008g0004a0001c0001t0008g0092a0001c0001t0026g0338others(2): Show | 6 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639+10814G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944059 | ||||||
chr2:173944073
|
G | C | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1639+10800C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944073 | ||||||
chr2:173944101
|
A | C | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG02886.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1639+10772T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944101 | ||||||
chr2:173944118
|
A | G | 1 | a0001c0001t0006g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1639+10755T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944118 | ||||||
chr2:173944171
|
T | C | 46 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(43): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1639+10702A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944171 | ||||||
chr2:173944197
|
T | C | 1 | a0001c0001t0008g0183 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1639+10676A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944197 | ||||||
chr2:173944216
|
G | A | 2 | a0001c0001t0012g0295a0001c0001t0090g0296 | 2 | HG00438.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1639+10657C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944216 | ||||||
chr2:173944232
|
C | T | 11 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(8): Show | 11 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1639+10641G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944232 | ||||||
chr2:173944262
|
G | A | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+10611C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944262 | ||||||
chr2:173944341
|
C | T | 1 | a0002c0002t0002g0240 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1639+10532G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944341 | ||||||
chr2:173944515
|
C | A | 1 | a0001c0001t0033g0066 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1639+10358G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944515 | ||||||
chr2:173944605
|
A | C | 37 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(34): Show | 37 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1639+10268T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944605 | ||||||
chr2:173944612
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+10261A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944612 | ||||||
chr2:173944637
|
C | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+10236G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944637 | ||||||
chr2:173944697
|
G | A | 2 | a0001c0001t0005g0035a0001c0001t0005g0036 | 2 | HG01106.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1639+10176C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944697 | ||||||
chr2:173944953
|
C | T | 4 | a0002c0002t0002g0070a0002c0002t0002g0210a0002c0002t0002g0250others(1): Show | 4 | NA18959.hp1 NA18973.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639+9920G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944953 | ||||||
chr2:173944997
|
T | C | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+9876A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173944997 | ||||||
chr2:173945135
|
G | C | 1 | a0001c0001t0065g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1639+9738C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173945135 | ||||||
chr2:173945258
|
C | CT | 3 | a0001c0001t0018g0321a0001c0001t0018g0322a0001c0001t0018g0323 | 3 | HG02559.hp1 HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1639+9614dupA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173945258 | ||||||
chr2:173945269
|
T | A | 1 | a0001c0001t0006g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1639+9604A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173945269 | ||||||
chr2:173945280
|
A | T | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 242 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.1639+9593T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173945280 | ||||||
chr2:173945370
|
A | G | 1 | a0001c0001t0005g0024 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1639+9503T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173945370 | ||||||
chr2:173945459
|
A | T | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+9414T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173945459 | ||||||
chr2:173945872
|
T | C | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1639+9001A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173945872 | ||||||
chr2:173946165
|
A | T | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 242 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.1639+8708T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946165 | ||||||
chr2:173946201
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+8672A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946201 | ||||||
chr2:173946242
|
A | T | 2 | a0001c0001t0006g0103a0001c0001t0006g0121 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1639+8631T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946242 | ||||||
chr2:173946309
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+8564A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946309 | ||||||
chr2:173946315
|
A | AT | 14 | a0001c0001t0008g0092a0001c0001t0012g0292a0001c0001t0012g0293others(11): Show | 14 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1639+8557dupA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946315 | ||||||
chr2:173946328
|
A | T | 2 | a0001c0001t0007g0120a0001c0001t0007g0122 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1639+8545T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946328 | ||||||
chr2:173946336
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1639+8537C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946336 | ||||||
chr2:173946363
|
T | TA | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+8509dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946363 | ||||||
chr2:173946493
|
C | T | 46 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(43): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1639+8380G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946493 | ||||||
chr2:173946721
|
C | CT | 51 | a0001c0001t0001g0013a0001c0001t0001g0126a0001c0001t0001g0329others(48): Show | 52 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1639+8151dupA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946721 | ||||||
chr2:173946721
|
C | CTT | 10 | a0001c0001t0005g0023a0001c0001t0009g0085a0001c0001t0009g0087others(7): Show | 10 | HG00735.hp2 HG02559.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1639+8150_1639+815 others(6): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946721 | ||||||
chr2:173946721
|
C | CTTTTTT | 4 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(1): Show | 6 | HG01257.hp1 HG01258.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639+8146_1639+815 others(10): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946721 | ||||||
chr2:173946721
|
CT | C | 18 | a0001c0001t0001g0187a0001c0001t0006g0103a0001c0001t0006g0121others(15): Show | 19 | HG01496.hp1 HG01515.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.1639+8151delA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946721 | ||||||
chr2:173946745
|
C | T | 11 | a0001c0001t0006g0103a0001c0001t0006g0121a0001c0001t0007g0120others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1639+8128G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946745 | ||||||
chr2:173946754
|
G | C | 4 | a0002c0002t0002g0214a0002c0002t0002g0263a0002c0002t0002g0265others(1): Show | 4 | HG02027.hp2 HG02074.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639+8119C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946754 | ||||||
chr2:173946865
|
G | A | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+8008C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946865 | ||||||
chr2:173946885
|
C | CTT | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(107): Show | 118 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1639+7986_1639+798 others(6): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173946885 | ||||||
chr2:173947088
|
C | T | 5 | a0001c0001t0008g0004a0001c0001t0008g0092a0001c0001t0026g0338others(2): Show | 6 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639+7785G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173947088 | ||||||
chr2:173947129
|
T | G | 24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 24 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1639+7744A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173947129 | ||||||
chr2:173947177
|
G | A | 2 | a0001c0001t0006g0103a0001c0001t0006g0121 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1639+7696C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173947177 | ||||||
chr2:173947507
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0329a0001c0001t0001g0330others(5): Show | 9 | HG00408.hp2 HG01928.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1639+7366A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173947507 | ||||||
chr2:173947594
|
T | C | 1 | a0001c0001t0007g0119 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1639+7279A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173947594 | ||||||
chr2:173947599
|
G | C | 20 | a0001c0001t0006g0107a0001c0001t0006g0110a0001c0001t0006g0111others(17): Show | 20 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.1639+7274C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173947599 | ||||||
chr2:173947688
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1639+7185C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173947688 | ||||||
chr2:173947852
|
T | C | 1 | a0002c0002t0002g0241 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1639+7021A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173947852 | ||||||
chr2:173947913
|
C | A | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1639+6960G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173947913 | ||||||
chr2:173947947
|
A | G | 1 | a0001c0001t0077g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1639+6926T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173947947 | ||||||
chr2:173948050
|
A | G | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+6823T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173948050 | ||||||
chr2:173948139
|
T | TTA | 4 | a0002c0002t0002g0215a0002c0002t0002g0216a0002c0002t0013g0267others(1): Show | 4 | NA18977.hp1 NA18978.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639+6732_1639+673 others(6): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173948139 | ||||||
chr2:173948324
|
T | C | 1 | a0002c0002t0020g0252 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1639+6549A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173948324 | ||||||
chr2:173948507
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1639+6366C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173948507 | ||||||
chr2:173948531
|
G | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+6342C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173948531 | ||||||
chr2:173948625
|
T | C | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG02886.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1639+6248A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173948625 | ||||||
chr2:173948730
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(111): Show | 123 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1639+6143C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173948730 | ||||||
chr2:173948761
|
AATAATT | A | 24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 24 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1639+6106_1639+611 others(10): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173948761 | ||||||
chr2:173948849
|
A | G | 1 | a0001c0001t0003g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1639+6024T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173948849 | ||||||
chr2:173949019
|
C | T | 1 | a0001c0001t0078g0039 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1639+5854G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949019 | ||||||
chr2:173949095
|
T | C | 1 | a0001c0001t0011g0052 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1639+5778A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949095 | ||||||
chr2:173949358
|
T | A | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+5515A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949358 | ||||||
chr2:173949366
|
G | GA | 37 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(34): Show | 39 | HG00735.hp2 HG00741.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.1639+5506dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949366 | ||||||
chr2:173949529
|
T | C | 2 | a0001c0001t0008g0004a0001c0001t0008g0092 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1639+5344A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949529 | ||||||
chr2:173949586
|
A | G | 1 | a0001c0001t0049g0203 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1639+5287T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949586 | ||||||
chr2:173949636
|
C | T | 24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 24 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1639+5237G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949636 | ||||||
chr2:173949704
|
C | CA | 10 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(7): Show | 10 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+5168dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949704 | ||||||
chr2:173949901
|
A | G | 3 | a0002c0002t0002g0208a0002c0002t0002g0251a0002c0002t0020g0252 | 3 | NA18955.hp2 NA18982.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1639+4972T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949901 | ||||||
chr2:173949948
|
G | T | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1639+4925C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949948 | ||||||
chr2:173949950
|
G | A | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+4923C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173949950 | ||||||
chr2:173950130
|
C | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+4743G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950130 | ||||||
chr2:173950132
|
C | A | 1 | a0001c0001t0010g0328 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1639+4741G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950132 | ||||||
chr2:173950177
|
G | T | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1639+4696C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950177 | ||||||
chr2:173950264
|
G | A | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1639+4609C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950264 | ||||||
chr2:173950317
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+4556A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950317 | ||||||
chr2:173950319
|
T | TA | 18 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(15): Show | 18 | HG00438.hp2 HG00621.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1639+4553dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950319 | ||||||
chr2:173950319
|
TA | T | 12 | a0001c0001t0001g0168a0001c0001t0001g0193a0001c0001t0022g0046others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1639+4553delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950319 | ||||||
chr2:173950465
|
G | A | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+4408C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950465 | ||||||
chr2:173950539
|
C | T | 1 | a0001c0001t0065g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1639+4334G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950539 | ||||||
chr2:173950607
|
G | A | 6 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(3): Show | 8 | HG01257.hp1 HG01258.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639+4266C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950607 | ||||||
chr2:173950658
|
T | TA | 6 | a0001c0001t0011g0052a0001c0001t0011g0055a0001c0001t0011g0056others(3): Show | 6 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1639+4214dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950658 | ||||||
chr2:173950658
|
TA | T | 9 | a0001c0001t0003g0270a0001c0001t0006g0111a0001c0001t0007g0120others(6): Show | 9 | HG01167.hp1 HG01975.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1639+4214delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950658 | ||||||
chr2:173950663
|
A | G | 2 | a0001c0001t0032g0014a0001c0001t0085g0042 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1639+4210T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950663 | ||||||
chr2:173950930
|
T | C | 10 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(7): Show | 10 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+3943A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173950930 | ||||||
chr2:173951024
|
T | C | 11 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(8): Show | 11 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1639+3849A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951024 | ||||||
chr2:173951170
|
A | C | 69 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(66): Show | 71 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1639+3703T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951170 | ||||||
chr2:173951312
|
C | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1639+3561G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951312 | ||||||
chr2:173951352
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1639+3521T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951352 | ||||||
chr2:173951400
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+3473A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951400 | ||||||
chr2:173951416
|
T | G | 46 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(43): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1639+3457A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951416 | ||||||
chr2:173951434
|
A | G | 2 | a0001c0001t0032g0014a0001c0001t0085g0042 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1639+3439T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951434 | ||||||
chr2:173951628
|
G | A | 82 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(79): Show | 84 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.1639+3245C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951628 | ||||||
chr2:173951728
|
C | A | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+3145G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951728 | ||||||
chr2:173951810
|
C | G | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+3063G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951810 | ||||||
chr2:173951893
|
A | G | 3 | a0001c0005t0074g0191a0001c0005t0097g0341a0001c0005t0098g0340 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1639+2980T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951893 | ||||||
chr2:173951933
|
C | G | 46 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(43): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1639+2940G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173951933 | ||||||
chr2:173952101
|
A | AT | 27 | a0001c0001t0001g0153a0001c0001t0001g0168a0001c0001t0001g0169others(24): Show | 30 | HG00735.hp2 HG01099.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1639+2771dupA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952101 | ||||||
chr2:173952101
|
A | ATT | 24 | a0001c0001t0005g0037a0001c0001t0009g0082a0001c0001t0011g0043others(21): Show | 24 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1639+2770_1639+277 others(6): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952101 | ||||||
chr2:173952101
|
A | ATTT | 22 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(19): Show | 22 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1639+2769_1639+277 others(7): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952101 | ||||||
chr2:173952101
|
AT | A | 28 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0332others(25): Show | 29 | HG01074.hp1 HG01255.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1639+2771delA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952101 | ||||||
chr2:173952120
|
G | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+2753C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952120 | ||||||
chr2:173952203
|
G | C | 1 | a0001c0001t0005g0038 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1639+2670C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952203 | ||||||
chr2:173952386
|
C | T | 1 | a0001c0001t0007g0090 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1639+2487G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952386 | ||||||
chr2:173952468
|
C | T | 1 | a0001c0001t0048g0202 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1639+2405G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952468 | ||||||
chr2:173952530
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+2343A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952530 | ||||||
chr2:173952619
|
A | G | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1639+2254T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952619 | ||||||
chr2:173952665
|
C | T | 59 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(56): Show | 61 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1639+2208G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952665 | ||||||
chr2:173952681
|
ATG | A | 6 | a0002c0002t0002g0011a0002c0002t0002g0065a0002c0002t0002g0217others(3): Show | 7 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639+2190_1639+219 others(6): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952681 | ||||||
chr2:173952772
|
C | G | 22 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1639+2101G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952772 | ||||||
chr2:173952834
|
G | A | 11 | a0001c0001t0006g0103a0001c0001t0006g0121a0001c0001t0007g0120others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1639+2039C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952834 | ||||||
chr2:173952900
|
A | G | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1639+1973T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173952900 | ||||||
chr2:173953011
|
G | A | 46 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(43): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1639+1862C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953011 | ||||||
chr2:173953221
|
G | A | 1 | a0001c0001t0064g0309 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1639+1652C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953221 | ||||||
chr2:173953298
|
A | G | 20 | a0001c0001t0006g0107a0001c0001t0006g0110a0001c0001t0006g0111others(17): Show | 20 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.1639+1575T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953298 | ||||||
chr2:173953355
|
C | A | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1639+1518G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953355 | ||||||
chr2:173953420
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1639+1453C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953420 | ||||||
chr2:173953465
|
AACTTTGG others(24): Show |
A | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+1377_1639+140 others(35): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953465 | ||||||
chr2:173953520
|
G | A | 2 | a0001c0001t0006g0123a0001c0001t0006g0124 | 2 | HG01071.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1639+1353C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953520 | ||||||
chr2:173953533
|
C | T | 1 | a0002c0002t0002g0249 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1639+1340G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953533 | ||||||
chr2:173953773
|
AC | A | 49 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(46): Show | 51 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1639+1099delG | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953773 | ||||||
chr2:173953774
|
C | A | 33 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(30): Show | 33 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.1639+1099G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953774 | ||||||
chr2:173953775
|
A | AAAC | 10 | a0001c0001t0011g0015a0001c0001t0022g0046a0001c0001t0022g0047others(7): Show | 10 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+1097_1639+109 others(7): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953775 | ||||||
chr2:173953775
|
A | C | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1639+1098T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953775 | ||||||
chr2:173953779
|
C | CA | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1639+1093dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953779 | ||||||
chr2:173953780
|
A | AAAC | 13 | a0001c0001t0009g0087a0001c0001t0011g0043a0001c0001t0011g0052others(10): Show | 13 | HG00741.hp1 HG01106.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1639+1092_1639+109 others(7): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953780 | ||||||
chr2:173953781
|
A | AAC | 12 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(9): Show | 14 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1639+1091_1639+109 others(6): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953781 | ||||||
chr2:173953782
|
A | AC | 37 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(34): Show | 37 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1639+1090_1639+109 others(5): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953782 | ||||||
chr2:173953783
|
A | C | 2 | a0001c0001t0087g0044a0001c0001t0096g0301 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1639+1090T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953783 | ||||||
chr2:173953783
|
AC | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0153a0001c0001t0001g0155others(2): Show | 5 | HG01074.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1639+1089delG | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953783 | ||||||
chr2:173953784
|
C | A | 65 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(62): Show | 67 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.1639+1089G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953784 | ||||||
chr2:173953784
|
CA | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(104): Show | 116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1639+1088delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953784 | ||||||
chr2:173953785
|
A | C | 6 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(3): Show | 8 | HG01257.hp1 HG01258.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639+1088T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953785 | ||||||
chr2:173953786
|
A | C | 24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 24 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1639+1087T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953786 | ||||||
chr2:173953790
|
A | C | 1 | a0001c0001t0029g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1639+1083T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953790 | ||||||
chr2:173953856
|
A | G | 5 | a0001c0001t0008g0004a0001c0001t0008g0092a0001c0001t0026g0338others(2): Show | 6 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639+1017T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173953856 | ||||||
chr2:173954163
|
C | T | 2 | a0002c0002t0002g0247a0002c0002t0002g0248 | 2 | NA18964.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1639+710G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173954163 | ||||||
chr2:173954195
|
T | C | 1 | a0001c0001t0005g0038 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1639+678A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173954195 | ||||||
chr2:173954242
|
C | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1639+631G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173954242 | ||||||
chr2:173954316
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(104): Show | 115 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1639+557C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173954316 | ||||||
chr2:173954403
|
C | T | 1 | a0001c0001t0014g0325 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1639+470G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173954403 | ||||||
chr2:173954482
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+391A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 4/6 | chr2 | 173954482 | ||||||
chr2:173956366
|
G | C | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.280-134C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956366 | ||||||
chr2:173956389
|
A | G | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.280-157T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956389 | ||||||
chr2:173956452
|
A | G | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-220T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956452 | ||||||
chr2:173956509
|
T | C | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.280-277A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956509 | ||||||
chr2:173956575
|
A | T | 1 | a0001c0001t0063g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.280-343T>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956575 | ||||||
chr2:173956619
|
G | T | 1 | a0001c0001t0007g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.280-387C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956619 | ||||||
chr2:173956684
|
G | A | 4 | a0001c0001t0016g0225a0001c0001t0040g0222a0001c0001t0092g0223others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-452C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956684 | ||||||
chr2:173956763
|
G | C | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.280-531C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956763 | ||||||
chr2:173956767
|
T | A | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.280-535A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956767 | ||||||
chr2:173956771
|
G | A | 1 | a0001c0001t0003g0283 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.280-539C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956771 | ||||||
chr2:173956914
|
C | A | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.280-682G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956914 | ||||||
chr2:173956964
|
T | C | 1 | a0001c0001t0007g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280-732A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173956964 | ||||||
chr2:173957093
|
T | C | 1 | a0001c0001t0003g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.280-861A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173957093 | ||||||
chr2:173957198
|
T | A | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.280-966A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173957198 | ||||||
chr2:173957224
|
C | T | 1 | a0002c0002t0002g0205 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.280-992G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173957224 | ||||||
chr2:173957613
|
C | T | 1 | a0001c0001t0033g0294 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.280-1381G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173957613 | ||||||
chr2:173957642
|
A | G | 1 | a0001c0001t0060g0125 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.280-1410T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173957642 | ||||||
chr2:173957807
|
A | G | 1 | a0002c0002t0002g0242 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.280-1575T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173957807 | ||||||
chr2:173957839
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.280-1607G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173957839 | ||||||
chr2:173957922
|
G | C | 1 | a0001c0001t0078g0039 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.280-1690C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173957922 | ||||||
chr2:173957932
|
T | G | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.280-1700A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173957932 | ||||||
chr2:173957933
|
C | G | 1 | a0001c0001t0006g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.280-1701G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173957933 | ||||||
chr2:173958104
|
C | G | 4 | a0002c0002t0002g0205a0002c0002t0002g0240a0002c0002t0002g0241others(1): Show | 4 | HG01981.hp2 NA18978.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-1872G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958104 | ||||||
chr2:173958270
|
G | GT | 18 | a0001c0001t0005g0023a0001c0001t0011g0015a0001c0001t0016g0225others(15): Show | 18 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.280-2039dupA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958270 | ||||||
chr2:173958270
|
GT | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(125): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.280-2039delA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958270 | ||||||
chr2:173958270
|
GTT | G | 45 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0185others(42): Show | 45 | HG00438.hp2 HG00621.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.280-2040_280-2039d others(4): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958270 | ||||||
chr2:173958322
|
C | T | 1 | a0001c0001t0003g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.280-2090G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958322 | ||||||
chr2:173958582
|
GA | G | 55 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(52): Show | 57 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.280-2351delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958582 | ||||||
chr2:173958583
|
A | G | 1 | a0001c0001t0038g0290 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.280-2351T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958583 | ||||||
chr2:173958617
|
AGAATC | A | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-2390_280-2386d others(7): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958617 | ||||||
chr2:173958685
|
C | A | 1 | a0001c0001t0024g0219 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.280-2453G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958685 | ||||||
chr2:173958687
|
C | T | 1 | a0001c0001t0071g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.280-2455G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958687 | ||||||
chr2:173958714
|
A | C | 1 | a0001c0001t0071g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.280-2482T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958714 | ||||||
chr2:173958748
|
C | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(229): Show | 244 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.280-2516G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958748 | ||||||
chr2:173958768
|
T | C | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.280-2536A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958768 | ||||||
chr2:173958778
|
GA | G | 7 | a0001c0001t0001g0165a0001c0001t0001g0329a0001c0001t0001g0330others(4): Show | 7 | HG00408.hp1 HG01123.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-2547delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958778 | ||||||
chr2:173958959
|
T | C | 5 | a0001c0001t0001g0162a0001c0001t0004g0061a0001c0001t0008g0161others(2): Show | 5 | NA18953.hp1 NA18959.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-2727A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173958959 | ||||||
chr2:173959016
|
G | C | 31 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.280-2784C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959016 | ||||||
chr2:173959302
|
C | G | 2 | a0001c0001t0034g0021a0001c0001t0034g0022 | 2 | HG00735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.280-3070G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959302 | ||||||
chr2:173959385
|
G | T | 5 | a0001c0001t0008g0004a0001c0001t0008g0092a0001c0001t0026g0338others(2): Show | 6 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-3153C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959385 | ||||||
chr2:173959445
|
G | T | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-3213C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959445 | ||||||
chr2:173959448
|
A | AG | 33 | a0001c0001t0006g0103a0001c0001t0006g0107a0001c0001t0006g0110others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.280-3217dupC | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959448 | ||||||
chr2:173959554
|
C | T | 62 | a0001c0001t0003g0244a0001c0001t0014g0067a0001c0001t0014g0071others(59): Show | 65 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.280-3322G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959554 | ||||||
chr2:173959582
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0137a0001c0001t0004g0138 | 3 | NA18954.hp2 NA19065.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.280-3350G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959582 | ||||||
chr2:173959802
|
G | A | 1 | a0001c0001t0015g0310 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.280-3570C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959802 | ||||||
chr2:173959857
|
G | A | 8 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(5): Show | 8 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.280-3625C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959857 | ||||||
chr2:173959899
|
C | G | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.280-3667G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959899 | ||||||
chr2:173959918
|
C | T | 1 | a0001c0001t0017g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.280-3686G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959918 | ||||||
chr2:173959941
|
A | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.280-3709T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173959941 | ||||||
chr2:173960031
|
G | A | 24 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(21): Show | 24 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.279+3730C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960031 | ||||||
chr2:173960098
|
T | C | 2 | a0001c0004t0007g0318a0001c0004t0007g0319 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.279+3663A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960098 | ||||||
chr2:173960157
|
G | A | 1 | a0001c0001t0011g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.279+3604C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960157 | ||||||
chr2:173960215
|
G | A | 1 | a0001c0001t0008g0092 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.279+3546C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960215 | ||||||
chr2:173960270
|
G | A | 5 | a0001c0001t0010g0328a0001c0001t0077g0190a0001c0005t0074g0191others(2): Show | 5 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+3491C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960270 | ||||||
chr2:173960362
|
G | A | 1 | a0002c0002t0002g0284 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.279+3399C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960362 | ||||||
chr2:173960445
|
T | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(60): Show | 71 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.279+3316A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960445 | ||||||
chr2:173960471
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | NA18974.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.279+3290C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960471 | ||||||
chr2:173960544
|
A | C | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+3217T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960544 | ||||||
chr2:173960677
|
T | C | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.279+3084A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960677 | ||||||
chr2:173960696
|
C | T | 1 | a0002c0002t0002g0205 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.279+3065G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960696 | ||||||
chr2:173960763
|
G | A | 1 | a0001c0005t0074g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.279+2998C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960763 | ||||||
chr2:173960813
|
A | C | 21 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(18): Show | 21 | HG00741.hp1 HG01123.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+2948T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960813 | ||||||
chr2:173960814
|
C | A | 21 | a0001c0001t0011g0015a0001c0001t0011g0043a0001c0001t0011g0052others(18): Show | 21 | HG00741.hp1 HG01123.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+2947G>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960814 | ||||||
chr2:173960814
|
C | CA | 27 | a0001c0001t0001g0187a0001c0001t0005g0016a0001c0001t0005g0017others(24): Show | 27 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.279+2946dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960814 | ||||||
chr2:173960840
|
G | A | 1 | a0001c0001t0007g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.279+2921C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960840 | ||||||
chr2:173960871
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0084g0041a0001c0001t0088g0051 | 3 | HG00741.hp1 HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.279+2890C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960871 | ||||||
chr2:173960913
|
C | T | 23 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(20): Show | 25 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.279+2848G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960913 | ||||||
chr2:173960931
|
G | A | 11 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0010g0096others(8): Show | 11 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.279+2830C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960931 | ||||||
chr2:173960934
|
C | T | 1 | a0002c0002t0042g0204 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.279+2827G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960934 | ||||||
chr2:173960989
|
T | A | 1 | a0001c0001t0068g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.279+2772A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173960989 | ||||||
chr2:173961079
|
G | C | 1 | a0001c0001t0011g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.279+2682C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961079 | ||||||
chr2:173961093
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.279+2668T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961093 | ||||||
chr2:173961103
|
T | C | 2 | a0001c0001t0007g0134a0001c0001t0007g0135 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.279+2658A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961103 | ||||||
chr2:173961159
|
C | T | 2 | a0001c0007t0008g0105a0001c0007t0008g0136 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.279+2602G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961159 | ||||||
chr2:173961650
|
T | C | 45 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(42): Show | 45 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.279+2111A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961650 | ||||||
chr2:173961744
|
T | C | 13 | a0001c0001t0010g0096a0001c0001t0010g0098a0001c0001t0010g0099others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.279+2017A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961744 | ||||||
chr2:173961794
|
G | C | 1 | a0001c0001t0001g0305 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.279+1967C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961794 | ||||||
chr2:173961838
|
T | C | 1 | a0001c0001t0077g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.279+1923A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961838 | ||||||
chr2:173961935
|
G | GT | 44 | a0001c0001t0003g0220a0001c0001t0003g0233a0001c0001t0003g0234others(41): Show | 45 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.279+1825dupA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961935 | ||||||
chr2:173961935
|
G | GTT | 6 | a0001c0001t0015g0306a0001c0001t0015g0307a0001c0001t0016g0291others(3): Show | 6 | HG01346.hp1 HG01975.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+1824_279+1825d others(4): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961935 | ||||||
chr2:173961935
|
GT | G | 17 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(14): Show | 20 | HG00099.hp1 HG00735.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.279+1825delA | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961935 | ||||||
chr2:173961937
|
T | TTTTTG | 10 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(7): Show | 10 | HG01884.hp1 HG02602.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+1823_279+1824i others(7): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961937 | ||||||
chr2:173961938
|
T | TTTTG | 21 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(18): Show | 21 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+1822_279+1823i others(6): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961938 | ||||||
chr2:173961939
|
T | TTTG | 10 | a0001c0001t0004g0060a0001c0001t0006g0103a0001c0001t0008g0004others(7): Show | 11 | HG00597.hp1 HG02523.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.279+1821_279+1822i others(5): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961939 | ||||||
chr2:173961940
|
T | TTG | 55 | a0001c0001t0001g0106a0001c0001t0001g0126a0001c0001t0001g0127others(52): Show | 55 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.279+1820_279+1821i others(4): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961940 | ||||||
chr2:173961941
|
T | TG | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(109): Show | 120 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.279+1819_279+1820i others(3): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961941 | ||||||
chr2:173961942
|
T | G | 4 | a0001c0001t0011g0056a0001c0001t0067g0199a0001c0001t0073g0080others(1): Show | 4 | HG00639.hp1 HG01169.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+1819A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961942 | ||||||
chr2:173961943
|
T | G | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.279+1818A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961943 | ||||||
chr2:173961944
|
T | G | 2 | a0001c0001t0001g0200a0001c0005t0074g0191 | 2 | HG02257.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.279+1817A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961944 | ||||||
chr2:173961947
|
T | G | 1 | a0001c0001t0006g0192 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.279+1814A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961947 | ||||||
chr2:173961949
|
T | G | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.279+1812A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961949 | ||||||
chr2:173961982
|
A | G | 1 | a0001c0001t0057g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.279+1779T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173961982 | ||||||
chr2:173962196
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.279+1565A>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173962196 | ||||||
chr2:173962300
|
T | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG00438.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.279+1461A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173962300 | ||||||
chr2:173962324
|
A | C | 1 | a0001c0001t0001g0329 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.279+1437T>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173962324 | ||||||
chr2:173962416
|
G | C | 8 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+1345C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173962416 | ||||||
chr2:173962539
|
G | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(228): Show | 242 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.279+1222C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173962539 | ||||||
chr2:173962588
|
A | G | 5 | a0001c0001t0008g0004a0001c0001t0008g0092a0001c0001t0026g0338others(2): Show | 6 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1173T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173962588 | ||||||
chr2:173962647
|
T | TA | 16 | a0001c0001t0001g0201a0001c0001t0009g0001a0001c0001t0009g0081others(13): Show | 18 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.279+1113dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173962647 | ||||||
chr2:173962647
|
TA | T | 10 | a0001c0001t0012g0292a0001c0001t0012g0293a0001c0001t0012g0295others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+1113delT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173962647 | ||||||
chr2:173962946
|
A | G | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.279+815T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173962946 | ||||||
chr2:173963051
|
C | T | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.279+710G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963051 | ||||||
chr2:173963142
|
A | G | 1 | a0001c0001t0007g0090 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.279+619T>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963142 | ||||||
chr2:173963173
|
C | CA | 23 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(20): Show | 25 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.279+587dupT | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963173 | ||||||
chr2:173963204
|
C | G | 1 | a0001c0001t0032g0014 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.279+557G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963204 | ||||||
chr2:173963234
|
T | C | 2 | a0001c0001t0011g0055a0001c0001t0011g0056 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.279+527A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963234 | ||||||
chr2:173963364
|
G | C | 46 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(43): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.279+397C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963364 | ||||||
chr2:173963418
|
C | T | 1 | a0001c0001t0070g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.279+343G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963418 | ||||||
chr2:173963452
|
G | A | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG02886.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.279+309C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963452 | ||||||
chr2:173963552
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.279+209C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963552 | ||||||
chr2:173963618
|
C | G | 13 | a0001c0001t0009g0001a0001c0001t0009g0081a0001c0001t0009g0082others(10): Show | 15 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.279+143G>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963618 | ||||||
chr2:173963653
|
G | A | 1 | a0001c0001t0014g0067 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.279+108C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963653 | ||||||
chr2:173963662
|
G | A | 8 | a0001c0001t0015g0068a0001c0001t0015g0306a0001c0001t0015g0307others(5): Show | 8 | HG00741.hp2 HG01346.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+99C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963662 | ||||||
chr2:173963682
|
G | A | 1 | a0001c0001t0010g0328 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.279+79C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963682 | ||||||
chr2:173963743
|
G | A | 2 | a0001c0001t0011g0057a0001c0001t0086g0058 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.279+18C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 3/6 | chr2 | 173963743 | ||||||
chr2:173963890
|
C | T | 2 | a0001c0001t0073g0080a0001c0001t0095g0079 | 2 | HG00639.hp1 HG01361.hp1 |
splice_region_variant&intron_variant | LOW | c.157-7G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 2/6 | chr2 | 173963890 | ||||||
chr2:173963919
|
GGGGAGGG others(6): Show |
G | 1 | a0002c0002t0019g0073 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.157-49_157-37delGC others(11): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 2/6 | chr2 | 173963919 | ||||||
chr2:173963923
|
A | AG | 6 | a0001c0001t0001g0076a0001c0001t0004g0077a0001c0001t0021g0059others(3): Show | 6 | HG00544.hp2 HG00597.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-41dupC | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 2/6 | chr2 | 173963923 | ||||||
chr2:173964134
|
T | C | 1 | a0001c0001t0010g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.157-251A>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 2/6 | chr2 | 173964134 | ||||||
chr2:173964157
|
C | T | 1 | a0001c0001t0047g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.156+248G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 2/6 | chr2 | 173964157 | ||||||
chr2:173964271
|
C | T | 1 | a0001c0001t0014g0071 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.156+134G>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 2/6 | chr2 | 173964271 | ||||||
chr2:173964294
|
G | T | 1 | a0002c0002t0002g0070 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.156+111C>A | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 2/6 | chr2 | 173964294 | ||||||
chr2:173964307
|
A | ACGAGGAG others(12): Show |
1 | a0001c0001t0001g0003 | 2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.156+79_156+97dupCC others(17): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 2/6 | chr2 | 173964307 | ||||||
chr2:173964568
|
C | CG | 11 | a0001c0001t0001g0064a0001c0001t0004g0060a0001c0001t0004g0061others(8): Show | 11 | HG00642.hp1 HG00642.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.8-16dupC | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173964568 | ||||||
chr2:173964576
|
T | G | 1 | a0001c0001t0015g0320 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.8-23A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173964576 | ||||||
chr2:173964595
|
G | A | 4 | a0001c0001t0018g0321a0001c0001t0018g0322a0001c0001t0018g0323others(1): Show | 4 | HG00735.hp2 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-42C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173964595 | ||||||
chr2:173964631
|
G | A | 1 | a0001c0001t0014g0325 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8-78C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173964631 | ||||||
chr2:173964684
|
C | CCGGCGG | 45 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0020others(42): Show | 45 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.8-137_8-132dupCCGC others(2): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173964684 | ||||||
chr2:173964684
|
CCGGCGGC others(5): Show |
C | 1 | a0001c0001t0007g0327 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.8-143_8-132delCCGC others(8): Show |
SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173964684 | ||||||
chr2:173964692
|
G | A | 1 | a0001c0001t0001g0326 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.8-139C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173964692 | ||||||
chr2:173965011
|
G | A | 1 | a0001c0001t0010g0328 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.7+154C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173965011 | ||||||
chr2:173965070
|
G | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0329a0001c0001t0001g0330others(5): Show | 9 | HG00408.hp2 HG01928.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+95C>G | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173965070 | ||||||
chr2:173965100
|
T | G | 1 | a0002c0002t0041g0336 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.7+65A>C | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173965100 | ||||||
chr2:173965123
|
G | A | 1 | a0001c0001t0091g0337 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.7+42C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173965123 | ||||||
chr2:173965145
|
G | A | 2 | a0001c0001t0026g0338a0001c0001t0026g0339 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7+20C>T | SP3 | ENSG00000172845.18 | transcript | ENST00000310015.12 | protein_coding | 1/6 | chr2 | 173965145 |