geneid | 6493 |
---|---|
ensemblid | ENSG00000159263.16 |
hgncid | 10883 |
symbol | SIM2 |
name | SIM bHLH transcription factor 2 |
refseq_nuc | NM_005069.6 |
refseq_prot | NP_005060.1 |
ensembl_nuc | ENST00000290399.11 |
ensembl_prot | ENSP00000290399.6 |
mane_status | MANE Select |
chr | chr21 |
start | 36699115 |
end | 36749917 |
strand | + |
ver | v1.2 |
region | chr21:36699115-36749917 |
region5000 | chr21:36694115-36754917 |
regionname0 | SIM2_chr21_36699115_36749917 |
regionname5000 | SIM2_chr21_36694115_36754917 |
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 | 1/0 | 667 | 346 | 85 | 62 | 159 | 12 | 27 | 116 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002 | 0/1 | 667 | 46 | 1 | 15 | 4 | 5 | 20 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0003 | 0/0 | 667 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0004 | 0/0 | 667 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0005 | 0/0 | 667 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0006 | 0/0 | 667 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0007 | 0/0 | 667 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0008 | 0/0 | 667 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
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 | 1/0 | 2004 | 218 | 39 | 41 | 115 | 8 | 14 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0002 | 0/0 | 2004 | 101 | 27 | 16 | 41 | 4 | 13 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0003 | 0/1 | 2004 | 43 | 1 | 14 | 4 | 5 | 18 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0004 | 0/0 | 2004 | 12 | 9 | 3 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0005 | 0/0 | 2004 | 5 | 3 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0006 | 0/0 | 2004 | 4 | 3 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0007 | 0/0 | 2004 | 4 | 4 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0008 | 0/0 | 2004 | 3 | 3 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0009 | 0/0 | 2004 | 3 | 0 | 1 | 0 | 1 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0010 | 0/0 | 2004 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0011 | 0/0 | 2004 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0012 | 0/0 | 2004 | 2 | 0 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0013 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0014 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0015 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0016 | 0/0 | 2004 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0017 | 0/0 | 2004 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0018 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0019 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0020 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0021 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0022 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
c0023 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
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 | 2458 | 114 | 14 | 26 | 62 | 7 | 5 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0002 | 0/0 | 2453 | 73 | 27 | 14 | 24 | 3 | 5 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0003 | 0/1 | 2457 | 40 | 5 | 12 | 2 | 3 | 17 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0004 | 0/0 | 2459 | 35 | 6 | 4 | 23 | 0 | 2 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0005 | 1/0 | 2458 | 24 | 3 | 2 | 17 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0006 | 0/0 | 2453 | 16 | 0 | 3 | 13 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0007 | 0/0 | 2458 | 15 | 1 | 7 | 3 | 1 | 3 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0008 | 0/0 | 2459 | 8 | 1 | 0 | 6 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0009 | 0/0 | 2457 | 6 | 6 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0010 | 0/0 | 2453 | 5 | 0 | 0 | 0 | 0 | 5 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0011 | 0/0 | 2458 | 5 | 4 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0012 | 0/0 | 2460 | 5 | 4 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0013 | 0/0 | 2458 | 5 | 4 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0014 | 0/0 | 2457 | 5 | 0 | 2 | 1 | 1 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0015 | 0/0 | 2453 | 4 | 2 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0016 | 0/0 | 2454 | 3 | 0 | 0 | 3 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0017 | 0/0 | 2457 | 3 | 3 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0018 | 0/0 | 2457 | 3 | 1 | 1 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0019 | 0/0 | 2457 | 3 | 0 | 0 | 1 | 0 | 2 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0020 | 0/0 | 2459 | 2 | 1 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0021 | 0/0 | 2458 | 2 | 2 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0022 | 0/0 | 2453 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0023 | 0/0 | 2453 | 2 | 0 | 0 | 1 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0024 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0025 | 0/0 | 2458 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0026 | 0/0 | 2458 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0027 | 0/0 | 2458 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0028 | 0/0 | 2453 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0029 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0030 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0031 | 0/0 | 2453 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0032 | 0/0 | 2453 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0033 | 0/0 | 2454 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0034 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0035 | 0/0 | 2453 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0036 | 0/0 | 2458 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0037 | 0/0 | 2459 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0038 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0039 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0040 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0041 | 0/0 | 2458 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0042 | 0/0 | 2453 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0043 | 0/0 | 2453 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0044 | 0/0 | 2453 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0045 | 0/0 | 2458 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0046 | 0/0 | 2453 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0047 | 0/0 | 2453 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0048 | 0/0 | 2453 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0049 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0050 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0051 | 0/0 | 2458 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0052 | 0/0 | 2459 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
t0053 | 0/0 | 2459 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
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 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
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 | 1/0 | 2004 | 218 | 39 | 41 | 115 | 8 | 14 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002 | 0/0 | 2004 | 101 | 27 | 16 | 41 | 4 | 13 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0004 | 0/0 | 2004 | 12 | 9 | 3 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0007 | 0/0 | 2004 | 4 | 4 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0008 | 0/0 | 2004 | 3 | 3 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0010 | 0/0 | 2004 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0012 | 0/0 | 2004 | 2 | 0 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0014 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0016 | 0/0 | 2004 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0018 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0021 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0003 | 0/1 | 2004 | 43 | 1 | 14 | 4 | 5 | 18 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0013 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0019 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0020 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0003c0005 | 0/0 | 2004 | 5 | 3 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0003c0023 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0004c0006 | 0/0 | 2004 | 4 | 3 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0004c0022 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0005c0009 | 0/0 | 2004 | 3 | 0 | 1 | 0 | 1 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0006c0011 | 0/0 | 2004 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0007c0017 | 0/0 | 2004 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0008c0015 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4461 | 109 | 13 | 25 | 60 | 6 | 5 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0002 | 0/0 | 4456 | 2 | 0 | 0 | 1 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0003 | 0/0 | 4460 | 3 | 3 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0004 | 0/0 | 4462 | 31 | 4 | 2 | 23 | 0 | 2 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0005 | 1/0 | 4461 | 23 | 2 | 2 | 17 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0007 | 0/0 | 4461 | 11 | 1 | 5 | 3 | 0 | 2 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0008 | 0/0 | 4462 | 7 | 0 | 0 | 6 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0009 | 0/0 | 4460 | 6 | 6 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0011 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0012 | 0/0 | 4463 | 2 | 2 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0013 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0018 | 0/0 | 4460 | 3 | 1 | 1 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0021 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0022 | 0/0 | 4456 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0024 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0025 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0026 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0027 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0028 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0036 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0037 | 0/0 | 4462 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0038 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0039 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0041 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0045 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0048 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0049 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0050 | 0/0 | 4463 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0051 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0001t0053 | 0/0 | 4462 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0002 | 0/0 | 4456 | 61 | 20 | 12 | 22 | 3 | 4 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0006 | 0/0 | 4456 | 13 | 0 | 3 | 10 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0010 | 0/0 | 4456 | 5 | 0 | 0 | 0 | 0 | 5 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0015 | 0/0 | 4456 | 2 | 1 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0016 | 0/0 | 4457 | 3 | 0 | 0 | 3 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0017 | 0/0 | 4460 | 3 | 3 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0020 | 0/0 | 4462 | 2 | 1 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0023 | 0/0 | 4456 | 2 | 0 | 0 | 1 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0029 | 0/0 | 4457 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0030 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0031 | 0/0 | 4456 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0032 | 0/0 | 4456 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0033 | 0/0 | 4457 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0042 | 0/0 | 4456 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0043 | 0/0 | 4456 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0044 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0046 | 0/0 | 4456 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0002t0047 | 0/0 | 4456 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0004t0002 | 0/0 | 4456 | 8 | 6 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0004t0015 | 0/0 | 4456 | 2 | 1 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0004t0034 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0004t0035 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0007t0001 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0007t0003 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0007t0012 | 0/0 | 4463 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0007t0013 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0008t0013 | 0/0 | 4461 | 3 | 3 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0010t0001 | 0/0 | 4461 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0012t0004 | 0/0 | 4462 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0012t0052 | 0/0 | 4462 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0014t0002 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0016t0006 | 0/0 | 4456 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0018t0040 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0001c0021t0005 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0003t0001 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0003t0003 | 0/1 | 4460 | 34 | 1 | 11 | 2 | 3 | 16 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0003t0007 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0003t0014 | 0/0 | 4460 | 5 | 0 | 2 | 1 | 1 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0003t0019 | 0/0 | 4460 | 2 | 0 | 0 | 1 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0013t0003 | 0/0 | 4460 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0019t0019 | 0/0 | 4460 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0002c0020t0003 | 0/0 | 4460 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0003c0005t0011 | 0/0 | 4461 | 3 | 2 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0003c0005t0012 | 0/0 | 4463 | 2 | 1 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0003c0023t0011 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0004c0006t0004 | 0/0 | 4462 | 3 | 2 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0004c0006t0008 | 0/0 | 4462 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0004c0022t0021 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0005c0009t0007 | 0/0 | 4461 | 3 | 0 | 1 | 0 | 1 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0006c0011t0006 | 0/0 | 4456 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0007c0017t0002 | 0/0 | 4456 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
a0008c0015t0001 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | copy fasta | chr21 | 36694115 | 36754917 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0004g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0005g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0007g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0007g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0007g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0007g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0007g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0007g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0007g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0007g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0007g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0008g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0009g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0009g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0009g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0009g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0012g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0012g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0013g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0018g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0018g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0018g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0021g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0022g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0022g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0024g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0025g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0026g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0027g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0028g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0036g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0037g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0038g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0039g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0041g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0045g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0048g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0049g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0050g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0051g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0001t0053g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0002g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0010g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0010g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0010g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0010g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0015g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0015g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0016g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0016g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0016g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0017g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0017g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0017g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0020g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0020g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0023g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0023g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0029g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0030g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0031g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0032g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0033g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0042g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0043g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0044g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0046g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0002t0047g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0002g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0015g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0015g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0034g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0004t0035g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0007t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0007t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0007t0012g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0007t0013g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0008t0013g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0008t0013g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0008t0013g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0010t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0010t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0012t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0012t0052g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0014t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0016t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0018t0040g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0001c0021t0005g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0003g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0007g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0014g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0014g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0014g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0014g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0014g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0019g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0003t0019g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0013t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0019t0019g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0002c0020t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0003c0005t0011g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0003c0005t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0003c0005t0011g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0003c0005t0012g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0003c0005t0012g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0003c0023t0011g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0004c0006t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0004c0006t0004g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0004c0006t0008g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0004c0022t0021g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0005c0009t0007g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0005c0009t0007g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0005c0009t0007g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0006c0011t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0006c0011t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0007c0017t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
a0008c0015t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0014 | g0353 | EUR | GBR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | GBR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0286 | EUR | GBR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0302 | EUR | GBR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0082 | EUR | FIN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00280 | hp2 | a0001 | c0001 | t0026 | g0314 | EUR | FIN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00323 | hp1 | a0002 | c0003 | t0003 | g0278 | EUR | FIN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00323 | hp2 | a0002 | c0003 | t0003 | g0081 | EUR | FIN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00423 | hp2 | a0001 | c0001 | t0038 | g0133 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0191 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0154 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00558 | hp2 | a0001 | c0001 | t0005 | g0195 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0185 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00621 | hp1 | a0007 | c0017 | t0002 | g0293 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00639 | hp1 | a0002 | c0003 | t0003 | g0051 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00642 | hp1 | a0002 | c0003 | t0007 | g0343 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00642 | hp2 | a0002 | c0003 | t0003 | g0029 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | CHS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00735 | hp1 | a0003 | c0005 | t0012 | g0394 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00735 | hp2 | a0001 | c0002 | t0006 | g0164 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00738 | hp1 | a0002 | c0003 | t0014 | g0341 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00738 | hp2 | a0002 | c0003 | t0003 | g0320 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00741 | hp1 | a0001 | c0001 | t0041 | g0054 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG00741 | hp2 | a0004 | c0006 | t0004 | g0387 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01069 | hp1 | a0002 | c0003 | t0014 | g0352 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01069 | hp2 | a0001 | c0002 | t0006 | g0007 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01070 | hp2 | a0002 | c0003 | t0003 | g0083 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01071 | hp1 | a0001 | c0002 | t0006 | g0007 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01074 | hp1 | a0001 | c0012 | t0004 | g0270 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01074 | hp2 | a0002 | c0003 | t0003 | g0068 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0267 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01081 | hp2 | a0001 | c0012 | t0052 | g0288 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01099 | hp2 | a0001 | c0001 | t0045 | g0344 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01106 | hp1 | a0001 | c0002 | t0015 | g0351 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01106 | hp2 | a0001 | c0001 | t0013 | g0328 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01109 | hp2 | a0002 | c0003 | t0003 | g0303 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01168 | hp2 | a0002 | c0003 | t0003 | g0308 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0098 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01175 | hp2 | a0002 | c0003 | t0003 | g0281 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01243 | hp1 | a0001 | c0004 | t0015 | g0347 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PUR | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0334 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0309 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0211 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01257 | hp1 | a0001 | c0004 | t0002 | g0012 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0212 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01258 | hp2 | a0001 | c0004 | t0002 | g0012 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01346 | hp2 | a0001 | c0001 | t0036 | g0001 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01358 | hp2 | a0002 | c0003 | t0003 | g0085 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0183 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0342 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01433 | hp2 | a0002 | c0020 | t0003 | g0305 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01496 | hp1 | a0002 | c0003 | t0003 | g0225 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01496 | hp2 | a0001 | c0001 | t0051 | g0167 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0059 | EUR | IBS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01515 | hp2 | a0001 | c0001 | t0018 | g0020 | EUR | IBS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01516 | hp1 | a0005 | c0009 | t0007 | g0338 | EUR | IBS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | IBS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0060 | EUR | IBS | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01884 | hp1 | a0001 | c0014 | t0002 | g0378 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01884 | hp2 | a0001 | c0002 | t0017 | g0345 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0297 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01891 | hp2 | a0002 | c0003 | t0003 | g0048 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01934 | hp1 | a0002 | c0003 | t0003 | g0232 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01952 | hp1 | a0003 | c0005 | t0011 | g0090 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01978 | hp1 | a0001 | c0001 | t0007 | g0335 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0194 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0269 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0295 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01993 | hp2 | a0008 | c0015 | t0001 | g0268 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02027 | hp2 | a0002 | c0003 | t0019 | g0161 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02040 | hp2 | a0002 | c0003 | t0014 | g0330 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02056 | hp1 | a0001 | c0002 | t0006 | g0174 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02071 | hp1 | a0002 | c0003 | t0003 | g0119 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02074 | hp1 | a0001 | c0001 | t0007 | g0332 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02074 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02080 | hp1 | a0006 | c0011 | t0006 | g0177 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02083 | hp1 | a0001 | c0002 | t0047 | g0120 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02132 | hp1 | a0001 | c0001 | t0005 | g0168 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02145 | hp1 | a0001 | c0002 | t0015 | g0340 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0385 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | CDX | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | CDX | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0304 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0377 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0374 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02273 | hp1 | a0001 | c0001 | t0018 | g0287 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02280 | hp2 | a0001 | c0001 | t0028 | g0390 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02300 | hp2 | a0001 | c0001 | t0025 | g0253 | AMR | PEL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0391 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0379 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02602 | hp2 | a0002 | c0003 | t0003 | g0224 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02615 | hp1 | a0004 | c0006 | t0008 | g0359 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0349 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02622 | hp1 | a0001 | c0004 | t0035 | g0370 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02622 | hp2 | a0001 | c0004 | t0015 | g0346 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0200 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02647 | hp1 | a0001 | c0008 | t0013 | g0386 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02647 | hp2 | a0001 | c0004 | t0002 | g0395 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02683 | hp1 | a0002 | c0003 | t0003 | g0317 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0363 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0372 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0366 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02735 | hp1 | a0002 | c0003 | t0003 | g0276 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02735 | hp2 | a0002 | c0003 | t0003 | g0028 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02738 | hp2 | a0002 | c0003 | t0003 | g0282 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02809 | hp1 | a0004 | c0006 | t0004 | g0013 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02809 | hp2 | a0001 | c0002 | t0017 | g0092 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02818 | hp1 | a0004 | c0006 | t0004 | g0013 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02818 | hp2 | a0001 | c0004 | t0002 | g0053 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0388 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02886 | hp2 | a0003 | c0005 | t0011 | g0380 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0206 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02895 | hp2 | a0001 | c0004 | t0034 | g0050 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02896 | hp1 | a0001 | c0008 | t0013 | g0384 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02896 | hp2 | a0001 | c0002 | t0017 | g0091 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02897 | hp1 | a0001 | c0008 | t0013 | g0383 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0389 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0373 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02965 | hp1 | a0001 | c0001 | t0049 | g0362 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0230 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02970 | hp1 | a0001 | c0007 | t0001 | g0369 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02976 | hp1 | a0003 | c0005 | t0012 | g0371 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02976 | hp2 | a0001 | c0004 | t0002 | g0323 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0298 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03017 | hp2 | a0002 | c0003 | t0003 | g0274 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0204 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03041 | hp2 | a0001 | c0007 | t0012 | g0393 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0202 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0325 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0360 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03195 | hp1 | a0001 | c0021 | t0005 | g0358 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0113 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03209 | hp2 | a0001 | c0002 | t0044 | g0316 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0392 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03239 | hp1 | a0002 | c0003 | t0003 | g0356 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03239 | hp2 | a0001 | c0002 | t0023 | g0165 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03453 | hp2 | a0001 | c0001 | t0018 | g0198 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03486 | hp1 | a0001 | c0001 | t0048 | g0361 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0337 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03490 | hp2 | a0002 | c0003 | t0003 | g0217 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03491 | hp1 | a0005 | c0009 | t0007 | g0339 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03491 | hp2 | a0001 | c0002 | t0010 | g0009 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03492 | hp1 | a0001 | c0002 | t0010 | g0009 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03492 | hp2 | a0002 | c0003 | t0003 | g0216 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03516 | hp1 | a0001 | c0007 | t0013 | g0381 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03516 | hp2 | a0001 | c0001 | t0024 | g0364 | AFR | ESN | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03540 | hp1 | a0001 | c0002 | t0030 | g0227 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03540 | hp2 | a0001 | c0001 | t0012 | g0327 | AFR | GWD | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03579 | hp1 | a0001 | c0001 | t0037 | g0354 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0187 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03654 | hp2 | a0001 | c0002 | t0020 | g0283 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0329 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03688 | hp1 | a0002 | c0003 | t0019 | g0188 | SAS | STU | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | STU | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03704 | hp1 | a0001 | c0002 | t0010 | g0014 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03704 | hp2 | a0001 | c0002 | t0010 | g0071 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03710 | hp1 | a0001 | c0001 | t0053 | g0078 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0065 | SAS | PJL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03831 | hp1 | a0002 | c0003 | t0003 | g0306 | SAS | BEB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03834 | hp1 | a0002 | c0003 | t0003 | g0041 | SAS | BEB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03834 | hp2 | a0001 | c0002 | t0033 | g0034 | SAS | BEB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03927 | hp1 | a0002 | c0003 | t0003 | g0291 | SAS | BEB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03927 | hp2 | a0002 | c0019 | t0019 | g0182 | SAS | BEB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03942 | hp1 | a0001 | c0001 | t0008 | g0181 | SAS | BEB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03942 | hp2 | a0002 | c0003 | t0003 | g0218 | SAS | BEB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG04115 | hp1 | a0002 | c0003 | t0014 | g0348 | SAS | STU | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG04115 | hp2 | a0001 | c0002 | t0043 | g0030 | SAS | STU | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG04184 | hp2 | a0002 | c0003 | t0003 | g0032 | SAS | BEB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG04199 | hp1 | a0002 | c0003 | t0003 | g0064 | SAS | STU | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG04199 | hp2 | a0002 | c0003 | t0003 | g0219 | SAS | STU | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG04204 | hp1 | a0001 | c0002 | t0010 | g0319 | SAS | STU | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0310 | SAS | STU | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0252 | SAS | STU | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG04228 | hp2 | a0002 | c0013 | t0003 | g0017 | SAS | STU | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18522 | hp1 | a0003 | c0005 | t0011 | g0149 | AFR | YRI | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18522 | hp2 | a0004 | c0022 | t0021 | g0063 | AFR | YRI | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18612 | hp1 | a0001 | c0016 | t0006 | g0153 | EAS | CHB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18747 | hp1 | a0001 | c0001 | t0008 | g0155 | EAS | CHB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | CHB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18906 | hp1 | a0001 | c0004 | t0002 | g0367 | AFR | YRI | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0375 | AFR | YRI | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18941 | hp1 | a0001 | c0001 | t0008 | g0172 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18942 | hp2 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18945 | hp1 | a0001 | c0002 | t0042 | g0118 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18954 | hp2 | a0001 | c0002 | t0023 | g0175 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18956 | hp2 | a0001 | c0002 | t0016 | g0079 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18961 | hp1 | a0001 | c0010 | t0001 | g0151 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18961 | hp2 | a0001 | c0002 | t0006 | g0186 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18969 | hp1 | a0001 | c0010 | t0001 | g0152 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18970 | hp2 | a0006 | c0011 | t0006 | g0176 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18979 | hp1 | a0001 | c0001 | t0039 | g0127 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18979 | hp2 | a0001 | c0001 | t0050 | g0166 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18984 | hp1 | a0002 | c0003 | t0003 | g0111 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18984 | hp2 | a0001 | c0002 | t0006 | g0173 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18985 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18986 | hp2 | a0001 | c0001 | t0007 | g0331 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18989 | hp1 | a0001 | c0001 | t0008 | g0171 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18990 | hp2 | a0001 | c0002 | t0006 | g0163 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18995 | hp1 | a0001 | c0001 | t0022 | g0141 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18995 | hp2 | a0001 | c0002 | t0016 | g0080 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19009 | hp2 | a0001 | c0002 | t0006 | g0189 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19011 | hp2 | a0001 | c0001 | t0007 | g0365 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0382 | AFR | LWK | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0355 | AFR | LWK | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19057 | hp1 | a0001 | c0001 | t0008 | g0162 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19057 | hp2 | a0001 | c0002 | t0006 | g0006 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19060 | hp1 | a0001 | c0002 | t0046 | g0333 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0157 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19066 | hp1 | a0001 | c0002 | t0006 | g0006 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19074 | hp1 | a0001 | c0002 | t0006 | g0160 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19079 | hp2 | a0001 | c0002 | t0006 | g0015 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19084 | hp2 | a0001 | c0001 | t0022 | g0121 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19086 | hp2 | a0001 | c0002 | t0031 | g0042 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19087 | hp1 | a0001 | c0001 | t0008 | g0193 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19087 | hp2 | a0001 | c0002 | t0029 | g0140 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19090 | hp1 | a0001 | c0002 | t0016 | g0096 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19090 | hp2 | a0001 | c0001 | t0008 | g0179 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19240 | hp1 | a0003 | c0023 | t0011 | g0368 | AFR | YRI | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ASW | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ASW | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA20752 | hp2 | a0001 | c0002 | t0032 | g0019 | EUR | TSI | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA20805 | hp1 | a0002 | c0003 | t0003 | g0285 | EUR | TSI | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA20805 | hp2 | a0002 | c0003 | t0001 | g0045 | EUR | TSI | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA20905 | hp1 | a0001 | c0001 | t0027 | g0046 | SAS | GIH | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0275 | SAS | GIH | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG01123 | hp2 | a0005 | c0009 | t0007 | g0336 | AMR | CLM | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0203 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0376 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02486 | hp1 | a0001 | c0004 | t0002 | g0052 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02486 | hp2 | a0001 | c0002 | t0020 | g0150 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02559 | hp1 | a0001 | c0018 | t0040 | g0146 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG02559 | hp2 | a0001 | c0007 | t0003 | g0024 | AFR | ACB | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | USA | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
HG06807 | hp2 | a0001 | c0001 | t0021 | g0326 | AFR | USA | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA18955 | hp2 | a0001 | c0002 | t0006 | g0192 | EAS | JPT | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0229 | AFR | USA | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0292 | AFR | USA | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA21309 | hp1 | a0001 | c0004 | t0002 | g0228 | AFR | LWK | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0003 | g0038 | REF | REF | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0190 | REF | REF | SIM2_chr21_36694115_36754917 | SIM2 | chr21 | 36694115 | 36754917 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:36709180
|
C | T | 1 | a0005 | 3 | HG01123.hp2 HG01516.hp1 HG03491.hp1 |
missense_variant | MODERATE | c.188C>T | p.Ala63Val | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/11 | 820/4461 | 188/2004 | 63/667 | chr21 | 36709180 | ||
chr21:36743448
|
G | A | 1 | a0008 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.1060G>A | p.Asp354Asn | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/11 | 1692/4461 | 1060/2004 | 354/667 | chr21 | 36743448 | ||
chr21:36745007
|
C | A | 1 | a0002 | 46 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(43): Show |
missense_variant | MODERATE | c.1447C>A | p.Leu483Met | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/11 | 2079/4461 | 1447/2004 | 483/667 | chr21 | 36745007 | ||
chr21:36747781
|
G | T | 1 | a0003 | 6 | HG00735.hp1 HG01952.hp1 HG02886.hp2 others(3): Show |
missense_variant | MODERATE | c.1693G>T | p.Ala565Ser | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 2325/4461 | 1693/2004 | 565/667 | chr21 | 36747781 | ||
chr21:36747812
|
G | A | 1 | a0006 | 2 | HG02080.hp1 NA18970.hp2 |
missense_variant | MODERATE | c.1724G>A | p.Arg575His | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 2356/4461 | 1724/2004 | 575/667 | chr21 | 36747812 | ||
chr21:36747925
|
G | T | 1 | a0007 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1837G>T | p.Gly613Trp | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 2469/4461 | 1837/2004 | 613/667 | chr21 | 36747925 | ||
chr21:36748066
|
T | C | 1 | a0004 | 5 | HG00741.hp2 HG02615.hp1 HG02809.hp1 others(2): Show |
missense_variant | MODERATE | c.1978T>C | p.Ser660Pro | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 2610/4461 | 1978/2004 | 660/667 | chr21 | 36748066 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:36699800
|
C | A | 1 | a0001c0010 | 2 | NA18961.hp1 NA18969.hp1 |
synonymous_variant | LOW | c.54C>A | p.Gly18Gly | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | 686/4461 | 54/2004 | 18/667 | chr21 | 36699800 | ||
chr21:36719859
|
T | C | 1 | a0002c0013 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.387T>C | p.His129His | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/11 | 1019/4461 | 387/2004 | 129/667 | chr21 | 36719859 | ||
chr21:36719871
|
C | T | 4 | a0001c0004a0001c0007a0003c0023others(1): Show | 18 | HG01243.hp1 HG01257.hp1 HG01258.hp2 others(15): Show |
synonymous_variant | LOW | c.399C>T | p.His133His | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/11 | 1031/4461 | 399/2004 | 133/667 | chr21 | 36719871 | ||
chr21:36726223
|
G | A | 1 | a0001c0014 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.648G>A | p.Ser216Ser | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/11 | 1280/4461 | 648/2004 | 216/667 | chr21 | 36726223 | ||
chr21:36731105
|
C | T | 1 | a0001c0021 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.804C>T | p.His268His | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/11 | 1436/4461 | 804/2004 | 268/667 | chr21 | 36731105 | ||
chr21:36744739
|
G | A | 6 | a0001c0002a0001c0004a0001c0014others(3): Show | 118 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(115): Show |
synonymous_variant | LOW | c.1179G>A | p.Ser393Ser | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/11 | 1811/4461 | 1179/2004 | 393/667 | chr21 | 36744739 | ||
chr21:36744946
|
G | A | 4 | a0001c0018a0001c0021a0004c0006others(1): Show | 7 | HG00741.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
synonymous_variant | LOW | c.1386G>A | p.Pro462Pro | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/11 | 2018/4461 | 1386/2004 | 462/667 | chr21 | 36744946 | ||
chr21:36745132
|
C | T | 1 | a0002c0020 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.1572C>T | p.Tyr524Tyr | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/11 | 2204/4461 | 1572/2004 | 524/667 | chr21 | 36745132 | ||
chr21:36747792
|
G | C | 1 | a0001c0012 | 2 | HG01074.hp1 HG01081.hp2 |
synonymous_variant | LOW | c.1704G>C | p.Gly568Gly | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 2336/4461 | 1704/2004 | 568/667 | chr21 | 36747792 | ||
chr21:36747807
|
G | C | 1 | a0002c0019 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.1719G>C | p.Leu573Leu | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 2351/4461 | 1719/2004 | 573/667 | chr21 | 36747807 | ||
chr21:36747888
|
C | T | 1 | a0001c0008 | 3 | HG02647.hp1 HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.1800C>T | p.Leu600Leu | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 2432/4461 | 1800/2004 | 600/667 | chr21 | 36747888 | ||
chr21:36747945
|
C | T | 1 | a0001c0016 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.1857C>T | p.Ala619Ala | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 2489/4461 | 1857/2004 | 619/667 | chr21 | 36747945 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:36699238
|
G | A | 1 | a0001c0001t0024 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-509G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | 509 | chr21 | 36699238 | |||||
chr21:36699276
|
C | G | 1 | a0001c0001t0024 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-471C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | 471 | chr21 | 36699276 | |||||
chr21:36699318
|
C | G | 1 | a0001c0001t0053 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-429C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | 429 | chr21 | 36699318 | |||||
chr21:36699337
|
C | T | 1 | a0001c0012t0052 | 1 | HG01081.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-410C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | chr21 | 36699337 | ||||||
chr21:36699365
|
G | A | 68 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(65): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
5_prime_UTR_variant | MODIFIER | c.-382G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | 382 | chr21 | 36699365 | |||||
chr21:36699444
|
G | A | 1 | a0001c0001t0025 | 1 | HG02300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-303G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | 303 | chr21 | 36699444 | |||||
chr21:36699539
|
G | T | 1 | a0001c0002t0047 | 1 | HG02083.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-208G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | chr21 | 36699539 | ||||||
chr21:36699688
|
A | G | 9 | a0001c0001t0007a0001c0001t0045a0001c0002t0015others(6): Show | 27 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-59A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | 59 | chr21 | 36699688 | |||||
chr21:36699703
|
G | A | 1 | a0001c0001t0026 | 1 | HG00280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | 44 | chr21 | 36699703 | |||||
chr21:36699708
|
G | A | 1 | a0001c0001t0027 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/11 | 39 | chr21 | 36699708 | |||||
chr21:36748140
|
G | T | 1 | a0001c0002t0043 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 48 | chr21 | 36748140 | |||||
chr21:36748248
|
C | G | 11 | a0001c0001t0003a0001c0001t0013a0001c0007t0003others(8): Show | 53 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*156C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 156 | chr21 | 36748248 | |||||
chr21:36748341
|
G | A | 4 | a0001c0001t0009a0001c0001t0028a0001c0001t0048others(1): Show | 9 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*249G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 249 | chr21 | 36748341 | |||||
chr21:36748396
|
A | G | 2 | a0001c0002t0042a0001c0002t0046 | 2 | NA18945.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*304A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 304 | chr21 | 36748396 | |||||
chr21:36748417
|
G | A | 25 | a0001c0001t0002a0001c0002t0002a0001c0002t0006others(22): Show | 115 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*325G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 325 | chr21 | 36748417 | |||||
chr21:36748606
|
C | T | 2 | a0001c0001t0041a0001c0018t0040 | 2 | HG00741.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*514C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 514 | chr21 | 36748606 | |||||
chr21:36748722
|
T | C | 1 | a0001c0001t0036 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*630T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 630 | chr21 | 36748722 | |||||
chr21:36748831
|
A | G | 1 | a0001c0001t0051 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*739A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 739 | chr21 | 36748831 | |||||
chr21:36748882
|
T | C | 1 | a0001c0002t0029 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*790T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 790 | chr21 | 36748882 | |||||
chr21:36749115
|
C | T | 1 | a0001c0001t0039 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1023C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1023 | chr21 | 36749115 | |||||
chr21:36749236
|
T | C | 41 | a0001c0001t0002a0001c0001t0003a0001c0001t0013others(38): Show | 177 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1144T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1144 | chr21 | 36749236 | |||||
chr21:36749271
|
G | A | 7 | a0001c0001t0011a0001c0001t0012a0001c0001t0037others(4): Show | 11 | HG00735.hp1 HG01952.hp1 HG02886.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1179G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1179 | chr21 | 36749271 | |||||
chr21:36749278
|
A | G | 1 | a0001c0001t0051 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1186A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1186 | chr21 | 36749278 | |||||
chr21:36749322
|
C | T | 1 | a0001c0001t0038 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1230C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1230 | chr21 | 36749322 | |||||
chr21:36749423
|
C | G | 1 | a0001c0002t0044 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1331C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1331 | chr21 | 36749423 | |||||
chr21:36749442
|
AACTG | A | 3 | a0001c0002t0016a0001c0002t0029a0001c0002t0033 | 5 | HG03834.hp2 NA18956.hp2 NA18995.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1354_*1357delGACT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1354 | INFO_REALIGN_3_PRIME | chr21 | 36749442 | ||||
chr21:36749444
|
CTGACT | C | 23 | a0001c0001t0002a0001c0001t0022a0001c0001t0028others(20): Show | 112 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1354_*1358delGACT others(1): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1354 | INFO_REALIGN_3_PRIME | chr21 | 36749444 | ||||
chr21:36749448
|
C | CT | 9 | a0001c0001t0004a0001c0001t0008a0001c0001t0037others(6): Show | 48 | HG00621.hp2 HG00673.hp2 HG00741.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1374dupT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1375 | INFO_REALIGN_3_PRIME | chr21 | 36749448 | ||||
chr21:36749448
|
C | CTT | 4 | a0001c0001t0012a0001c0001t0050a0001c0007t0012others(1): Show | 6 | HG00735.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1373_*1374dupTT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1375 | INFO_REALIGN_3_PRIME | chr21 | 36749448 | ||||
chr21:36749448
|
CT | C | 14 | a0001c0001t0003a0001c0001t0009a0001c0001t0018others(11): Show | 63 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1374delT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1374 | INFO_REALIGN_3_PRIME | chr21 | 36749448 | ||||
chr21:36749466
|
T | G | 1 | a0001c0001t0041 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1374T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1374 | chr21 | 36749466 | |||||
chr21:36749583
|
G | A | 2 | a0001c0002t0010a0001c0002t0033 | 6 | HG03491.hp2 HG03492.hp1 HG03704.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1491G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1491 | chr21 | 36749583 | |||||
chr21:36749605
|
G | A | 1 | a0001c0001t0045 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1513G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1513 | chr21 | 36749605 | |||||
chr21:36749677
|
C | T | 1 | a0001c0002t0032 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1585C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1585 | chr21 | 36749677 | |||||
chr21:36749790
|
A | G | 1 | a0001c0002t0031 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1698A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1698 | chr21 | 36749790 | |||||
chr21:36749870
|
T | C | 1 | a0001c0001t0037 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 11/11 | 1778 | chr21 | 36749870 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:36699998
|
C | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0379a0001c0001t0004g0002others(25): Show | 31 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.175+77C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36699998 | ||||||
chr21:36700011
|
T | A | 1 | a0001c0002t0010g0014 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.175+90T>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700011 | ||||||
chr21:36700056
|
G | C | 133 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(130): Show | 136 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.175+135G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700056 | ||||||
chr21:36700117
|
C | A | 2 | a0001c0001t0005g0144a0001c0001t0005g0145 | 2 | NA18959.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.175+196C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700117 | ||||||
chr21:36700128
|
T | C | 4 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0018t0040g0146others(1): Show | 4 | HG02280.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+207T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700128 | ||||||
chr21:36700132
|
C | T | 1 | a0001c0002t0002g0143 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.175+211C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700132 | ||||||
chr21:36700154
|
C | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0379a0001c0001t0004g0002others(26): Show | 32 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.175+233C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700154 | ||||||
chr21:36700195
|
G | T | 16 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(13): Show | 16 | HG00423.hp2 HG00673.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.175+274G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700195 | ||||||
chr21:36700279
|
A | AT | 337 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(334): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.175+365dupT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36700279 | |||||
chr21:36700299
|
C | CCTTT | 15 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0199others(12): Show | 15 | HG02280.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.175+393_175+396dup others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36700299 | |||||
chr21:36700316
|
CTCTT | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0379a0001c0001t0004g0002others(26): Show | 32 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.175+401_175+404del others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36700316 | |||||
chr21:36700392
|
C | T | 3 | a0001c0001t0003g0147a0001c0001t0003g0148a0003c0005t0011g0149 | 3 | HG02280.hp1 HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.175+471C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700392 | ||||||
chr21:36700423
|
G | T | 1 | a0001c0001t0007g0365 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.175+502G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700423 | ||||||
chr21:36700465
|
A | C | 1 | a0001c0001t0024g0364 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.175+544A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700465 | ||||||
chr21:36700472
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0021others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.175+551T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700472 | ||||||
chr21:36700518
|
C | T | 1 | a0002c0003t0003g0356 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.175+597C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700518 | ||||||
chr21:36700527
|
T | G | 1 | a0001c0016t0006g0153 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.175+606T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700527 | ||||||
chr21:36700756
|
C | G | 4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0007g0355others(1): Show | 4 | HG02630.hp1 HG03453.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+835C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700756 | ||||||
chr21:36700775
|
G | A | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0018g0198 | 3 | HG02630.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.175+854G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700775 | ||||||
chr21:36700872
|
G | C | 16 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0002g0210others(13): Show | 16 | HG01099.hp1 HG01123.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.175+951G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700872 | ||||||
chr21:36700986
|
C | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0021others(211): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.175+1065C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36700986 | ||||||
chr21:36701002
|
C | T | 6 | a0001c0001t0001g0094a0001c0001t0003g0093a0001c0001t0007g0355others(3): Show | 6 | HG01952.hp1 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+1081C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701002 | ||||||
chr21:36701071
|
T | A | 3 | a0001c0001t0001g0322a0001c0002t0002g0010a0001c0004t0002g0323 | 4 | HG01975.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+1150T>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701071 | ||||||
chr21:36701166
|
C | G | 2 | a0001c0002t0002g0010a0001c0004t0002g0323 | 3 | HG01975.hp2 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.175+1245C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701166 | ||||||
chr21:36701273
|
G | A | 1 | a0002c0013t0003g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.175+1352G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701273 | ||||||
chr21:36701360
|
TTGTGCTG others(82): Show |
T | 1 | a0001c0002t0002g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.175+1440_175+1528d others(91): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701360 | ||||||
chr21:36701369
|
C | CCGCTGGG others(4): Show |
1 | a0001c0001t0004g0018 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.175+1449_175+1459d others(13): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36701369 | |||||
chr21:36701395
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0097others(103): Show | 109 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.175+1474G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701395 | ||||||
chr21:36701404
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.175+1483C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701404 | ||||||
chr21:36701413
|
C | A | 3 | a0001c0002t0002g0010a0001c0004t0002g0323a0003c0005t0011g0090 | 4 | HG01952.hp1 HG01975.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+1492C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701413 | ||||||
chr21:36701451
|
C | A | 1 | a0001c0018t0040g0146 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.175+1530C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701451 | ||||||
chr21:36701513
|
TG | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0021others(113): Show | 119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.175+1594delG | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36701513 | |||||
chr21:36701639
|
C | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG00544.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.175+1718C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701639 | ||||||
chr21:36701660
|
C | T | 2 | a0001c0001t0001g0199a0001c0002t0002g0200 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.175+1739C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701660 | ||||||
chr21:36701693
|
G | A | 1 | a0001c0007t0003g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.175+1772G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701693 | ||||||
chr21:36701706
|
T | G | 53 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0031others(50): Show | 54 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.175+1785T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701706 | ||||||
chr21:36701769
|
A | G | 15 | a0001c0001t0001g0099a0001c0001t0001g0196a0001c0001t0001g0197others(12): Show | 16 | HG00099.hp1 HG01069.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.175+1848A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701769 | ||||||
chr21:36701790
|
C | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(147): Show | 155 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.175+1869C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701790 | ||||||
chr21:36701896
|
A | G | 2 | a0001c0002t0002g0010a0001c0004t0002g0323 | 3 | HG01975.hp2 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.175+1975A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701896 | ||||||
chr21:36701905
|
T | C | 8 | a0001c0001t0001g0112a0001c0001t0001g0220a0001c0001t0008g0162others(5): Show | 8 | HG02027.hp2 NA18963.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+1984T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701905 | ||||||
chr21:36701940
|
G | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0021others(219): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.175+2019G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701940 | ||||||
chr21:36701953
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0066others(106): Show | 113 | HG00140.hp2 HG00558.hp2 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.175+2032C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36701953 | ||||||
chr21:36702005
|
G | A | 3 | a0001c0001t0012g0113a0001c0001t0037g0354a0001c0002t0017g0091 | 3 | HG02896.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175+2084G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36702005 | ||||||
chr21:36702445
|
C | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0055others(92): Show | 98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.175+2524C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36702445 | ||||||
chr21:36702606
|
ACTGGTCA others(2): Show |
A | 4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0009g0391others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+2688_175+2696d others(11): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36702606 | |||||
chr21:36702644
|
G | C | 56 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0072others(53): Show | 57 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.175+2723G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36702644 | ||||||
chr21:36702712
|
G | A | 1 | a0001c0001t0007g0365 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.175+2791G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36702712 | ||||||
chr21:36702750
|
G | A | 4 | a0001c0002t0002g0208a0001c0002t0002g0375a0001c0002t0015g0340others(1): Show | 4 | HG01123.hp1 HG02145.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+2829G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36702750 | ||||||
chr21:36702804
|
C | T | 10 | a0001c0002t0002g0373a0001c0002t0020g0150a0001c0004t0002g0228others(7): Show | 11 | HG00735.hp1 HG00741.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.175+2883C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36702804 | ||||||
chr21:36702843
|
A | T | 1 | a0001c0001t0001g0301 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.175+2922A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36702843 | ||||||
chr21:36702922
|
G | C | 1 | a0001c0001t0037g0354 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.175+3001G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36702922 | ||||||
chr21:36702939
|
G | GA | 31 | a0001c0001t0001g0008a0001c0001t0001g0286a0001c0001t0001g0302others(28): Show | 32 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.175+3020dupA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36702939 | |||||
chr21:36702939
|
G | GAA | 9 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0003g0147others(6): Show | 10 | HG01975.hp2 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+3019_175+3020d others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36702939 | |||||
chr21:36702939
|
G | GAAAA | 12 | a0001c0001t0001g0311a0001c0001t0004g0065a0001c0001t0004g0243others(9): Show | 12 | HG01168.hp2 HG01515.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+3020_175+3021i others(6): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36702939 | |||||
chr21:36702939
|
G | GAAAAA | 160 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(157): Show | 166 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.175+3020_175+3021i others(7): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36702939 | |||||
chr21:36702939
|
G | GAAAAAA | 6 | a0001c0001t0001g0260a0001c0001t0007g0342a0001c0001t0009g0372others(3): Show | 6 | HG00735.hp2 HG01433.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+3020_175+3021i others(8): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36702939 | |||||
chr21:36702942
|
G | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0025others(216): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.175+3021G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36702942 | ||||||
chr21:36702942
|
G | GA | 53 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0094others(50): Show | 56 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.175+3034dupA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36702942 | |||||
chr21:36702958
|
A | T | 1 | a0001c0002t0029g0140 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.175+3037A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36702958 | ||||||
chr21:36703013
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0055others(86): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.175+3092G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703013 | ||||||
chr21:36703070
|
G | C | 4 | a0001c0002t0002g0208a0001c0002t0002g0375a0001c0002t0015g0340others(1): Show | 4 | HG01123.hp1 HG02145.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+3149G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703070 | ||||||
chr21:36703299
|
C | T | 2 | a0001c0001t0003g0147a0001c0001t0003g0148 | 2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.175+3378C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703299 | ||||||
chr21:36703311
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.175+3390C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703311 | ||||||
chr21:36703325
|
A | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0025others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.175+3404A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703325 | ||||||
chr21:36703327
|
C | T | 2 | a0001c0001t0007g0334a0001c0001t0007g0335 | 2 | HG01255.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.175+3406C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703327 | ||||||
chr21:36703340
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0025others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.175+3419T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703340 | ||||||
chr21:36703382
|
G | C | 2 | a0001c0002t0002g0208a0001c0002t0044g0316 | 2 | HG01123.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.175+3461G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703382 | ||||||
chr21:36703404
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0280a0001c0001t0001g0286others(13): Show | 17 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(14): Show |
intron_variant | MODIFIER | c.175+3483G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703404 | ||||||
chr21:36703581
|
T | C | 16 | a0001c0001t0001g0350a0001c0001t0004g0279a0001c0001t0004g0297others(13): Show | 17 | HG00741.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.175+3660T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703581 | ||||||
chr21:36703640
|
C | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(302): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.175+3719C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703640 | ||||||
chr21:36703655
|
G | A | 2 | a0005c0009t0007g0336a0005c0009t0007g0338 | 2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.175+3734G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703655 | ||||||
chr21:36703661
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0280a0001c0001t0001g0286others(9): Show | 13 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+3740G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703661 | ||||||
chr21:36703712
|
G | A | 1 | a0001c0002t0002g0208 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.175+3791G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703712 | ||||||
chr21:36703732
|
G | T | 29 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0012g0327others(26): Show | 30 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.175+3811G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703732 | ||||||
chr21:36703756
|
C | T | 3 | a0001c0001t0001g0199a0001c0002t0002g0200a0001c0002t0002g0349 | 3 | HG02615.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.175+3835C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703756 | ||||||
chr21:36703801
|
A | G | 4 | a0001c0002t0002g0208a0001c0002t0002g0375a0001c0002t0015g0340others(1): Show | 4 | HG01123.hp1 HG02145.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+3880A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703801 | ||||||
chr21:36703805
|
G | A | 1 | a0001c0002t0044g0316 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.175+3884G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703805 | ||||||
chr21:36703807
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(173): Show | 183 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+3886G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703807 | ||||||
chr21:36703874
|
G | A | 1 | a0001c0001t0007g0355 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+3953G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703874 | ||||||
chr21:36703916
|
A | C | 6 | a0001c0002t0002g0208a0001c0002t0002g0375a0001c0002t0015g0340others(3): Show | 6 | HG01123.hp1 HG02145.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+3995A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703916 | ||||||
chr21:36703978
|
C | T | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(281): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.175+4057C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36703978 | ||||||
chr21:36704023
|
C | G | 25 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0012g0327others(22): Show | 26 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.175+4102C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36704023 | ||||||
chr21:36704062
|
G | C | 2 | a0001c0001t0011g0204a0003c0005t0011g0149 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.175+4141G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36704062 | ||||||
chr21:36704068
|
G | A | 1 | a0001c0002t0002g0373 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+4147G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36704068 | ||||||
chr21:36704103
|
G | A | 1 | a0001c0001t0004g0392 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175+4182G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36704103 | ||||||
chr21:36704195
|
C | T | 1 | a0001c0001t0007g0342 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.175+4274C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36704195 | ||||||
chr21:36704200
|
G | A | 3 | a0001c0001t0004g0065a0001c0001t0008g0181a0001c0002t0002g0298 | 3 | HG03017.hp1 HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.175+4279G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36704200 | ||||||
chr21:36704501
|
G | A | 1 | a0001c0001t0007g0342 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.175+4580G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36704501 | ||||||
chr21:36704718
|
G | A | 1 | a0001c0002t0002g0208 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.176-4450G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36704718 | ||||||
chr21:36704787
|
C | T | 5 | a0001c0001t0018g0198a0001c0002t0002g0373a0001c0007t0013g0381others(2): Show | 6 | HG00741.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-4381C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36704787 | ||||||
chr21:36704984
|
G | A | 1 | a0001c0002t0002g0208 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.176-4184G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36704984 | ||||||
chr21:36705168
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(280): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.176-4000A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36705168 | ||||||
chr21:36705210
|
C | T | 19 | a0001c0001t0001g0350a0001c0001t0004g0279a0001c0001t0004g0297others(16): Show | 20 | HG00741.hp2 HG01123.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.176-3958C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36705210 | ||||||
chr21:36705212
|
C | T | 2 | a0001c0002t0020g0150a0001c0004t0002g0395 | 2 | HG02486.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.176-3956C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36705212 | ||||||
chr21:36705244
|
G | T | 59 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0075others(56): Show | 60 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.176-3924G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36705244 | ||||||
chr21:36705260
|
G | A | 1 | a0002c0003t0003g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.176-3908G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36705260 | ||||||
chr21:36705464
|
A | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0280a0001c0001t0001g0286others(14): Show | 19 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(16): Show |
intron_variant | MODIFIER | c.176-3704A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36705464 | ||||||
chr21:36705703
|
G | C | 3 | a0001c0001t0001g0209a0001c0001t0002g0210a0001c0002t0002g0221 | 3 | HG02148.hp2 HG02683.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.176-3465G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36705703 | ||||||
chr21:36705801
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.176-3367G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36705801 | ||||||
chr21:36705980
|
C | T | 61 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0075others(58): Show | 62 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.176-3188C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36705980 | ||||||
chr21:36706115
|
C | G | 10 | a0001c0001t0009g0372a0001c0001t0009g0388a0001c0001t0009g0389others(7): Show | 10 | HG01123.hp1 HG02145.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.176-3053C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36706115 | ||||||
chr21:36706191
|
A | C | 15 | a0001c0001t0001g0322a0001c0001t0001g0379a0001c0001t0009g0203others(12): Show | 15 | HG01433.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.176-2977A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36706191 | ||||||
chr21:36706253
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(203): Show | 213 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.176-2915C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36706253 | ||||||
chr21:36706326
|
C | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(97): Show | 105 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.176-2842C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36706326 | ||||||
chr21:36706362
|
C | T | 5 | a0001c0001t0018g0198a0001c0002t0002g0373a0001c0007t0013g0381others(2): Show | 6 | HG00741.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-2806C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36706362 | ||||||
chr21:36706389
|
C | A | 1 | a0001c0002t0002g0143 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.176-2779C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36706389 | ||||||
chr21:36706482
|
G | T | 1 | a0001c0001t0001g0040 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.176-2686G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36706482 | ||||||
chr21:36706702
|
G | A | 9 | a0001c0001t0009g0372a0001c0001t0009g0388a0001c0001t0009g0389others(6): Show | 9 | HG01123.hp1 HG02145.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.176-2466G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36706702 | ||||||
chr21:36706754
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.176-2414G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36706754 | ||||||
chr21:36706808
|
C | T | 2 | a0001c0002t0002g0292a0001c0002t0006g0007 | 3 | HG01069.hp2 HG01071.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.176-2360C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36706808 | ||||||
chr21:36707029
|
G | C | 1 | a0001c0001t0028g0390 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.176-2139G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707029 | ||||||
chr21:36707093
|
C | T | 4 | a0001c0002t0002g0208a0001c0002t0002g0375a0001c0002t0015g0340others(1): Show | 4 | HG01123.hp1 HG02145.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-2075C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707093 | ||||||
chr21:36707102
|
C | A | 1 | a0001c0004t0034g0050 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.176-2066C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707102 | ||||||
chr21:36707546
|
A | G | 1 | a0001c0004t0035g0370 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.176-1622A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707546 | ||||||
chr21:36707586
|
G | T | 1 | a0001c0001t0005g0180 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.176-1582G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707586 | ||||||
chr21:36707587
|
T | G | 1 | a0002c0003t0014g0341 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.176-1581T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707587 | ||||||
chr21:36707634
|
A | G | 3 | a0001c0002t0002g0374a0002c0003t0003g0051a0003c0005t0011g0090 | 3 | HG00639.hp1 HG01952.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.176-1534A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707634 | ||||||
chr21:36707637
|
G | A | 1 | a0001c0001t0005g0180 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.176-1531G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707637 | ||||||
chr21:36707654
|
C | A | 8 | a0001c0001t0001g0086a0001c0002t0002g0056a0001c0002t0002g0057others(5): Show | 8 | HG01192.hp1 HG01243.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-1514C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707654 | ||||||
chr21:36707964
|
C | G | 1 | a0001c0001t0004g0243 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.176-1204C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707964 | ||||||
chr21:36707969
|
C | G | 1 | a0001c0001t0004g0243 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.176-1199C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707969 | ||||||
chr21:36707970
|
C | CCGCAGTT others(18): Show |
1 | a0001c0001t0004g0102 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.176-1197_176-1196i others(27): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36707970 | |||||
chr21:36707970
|
C | CCGCAGTT others(18): Show |
294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(291): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.176-1197_176-1196i others(27): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36707970 | |||||
chr21:36707970
|
C | CCTGGCCC others(24): Show |
1 | a0001c0001t0004g0243 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.176-1197_176-1196i others(33): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 36707970 | |||||
chr21:36707973
|
G | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(293): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.176-1195G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36707973 | ||||||
chr21:36708018
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(301): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.176-1150T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708018 | ||||||
chr21:36708287
|
T | G | 1 | a0001c0001t0005g0169 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.176-881T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708287 | ||||||
chr21:36708322
|
T | G | 1 | a0001c0001t0001g0261 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.176-846T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708322 | ||||||
chr21:36708439
|
C | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(301): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.176-729C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708439 | ||||||
chr21:36708454
|
A | G | 1 | a0003c0005t0012g0371 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.176-714A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708454 | ||||||
chr21:36708479
|
C | G | 10 | a0001c0001t0009g0372a0001c0001t0009g0388a0001c0001t0009g0389others(7): Show | 11 | HG00741.hp2 HG02723.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-689C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708479 | ||||||
chr21:36708536
|
C | G | 1 | a0001c0001t0007g0365 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.176-632C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708536 | ||||||
chr21:36708600
|
G | A | 1 | a0001c0002t0002g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.176-568G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708600 | ||||||
chr21:36708616
|
A | T | 1 | a0001c0001t0012g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.176-552A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708616 | ||||||
chr21:36708673
|
G | A | 1 | a0001c0002t0002g0382 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-495G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708673 | ||||||
chr21:36708800
|
C | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0280a0001c0001t0001g0286others(8): Show | 12 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(9): Show |
intron_variant | MODIFIER | c.176-368C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708800 | ||||||
chr21:36708866
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.176-302G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708866 | ||||||
chr21:36708942
|
G | C | 1 | a0002c0003t0003g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.176-226G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36708942 | ||||||
chr21:36709096
|
C | A | 20 | a0001c0001t0001g0073a0001c0001t0001g0135a0001c0001t0001g0138others(17): Show | 20 | HG00673.hp1 HG01167.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.176-72C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 1/10 | chr21 | 36709096 | ||||||
chr21:36709262
|
T | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(302): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.258+12T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36709262 | ||||||
chr21:36709277
|
C | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(296): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.258+27C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36709277 | ||||||
chr21:36709312
|
C | T | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.258+62C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36709312 | ||||||
chr21:36709598
|
G | A | 2 | a0001c0001t0037g0354a0001c0001t0049g0362 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.258+348G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36709598 | ||||||
chr21:36709600
|
G | T | 1 | a0001c0001t0004g0325 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.258+350G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36709600 | ||||||
chr21:36709666
|
G | A | 2 | a0001c0001t0037g0354a0001c0001t0049g0362 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.258+416G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36709666 | ||||||
chr21:36709767
|
T | C | 4 | a0001c0002t0002g0208a0001c0002t0002g0375a0001c0002t0015g0340others(1): Show | 4 | HG01123.hp1 HG02145.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+517T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36709767 | ||||||
chr21:36709882
|
G | T | 1 | a0001c0001t0005g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.258+632G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36709882 | ||||||
chr21:36709968
|
G | A | 23 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0012g0327others(20): Show | 23 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.258+718G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36709968 | ||||||
chr21:36710402
|
C | A | 2 | a0001c0002t0002g0366a0001c0002t0002g0382 | 2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.258+1152C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36710402 | ||||||
chr21:36710432
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.258+1182C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36710432 | ||||||
chr21:36710512
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(219): Show | 229 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.258+1262C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36710512 | ||||||
chr21:36710601
|
A | G | 1 | a0001c0002t0006g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.258+1351A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36710601 | ||||||
chr21:36710605
|
T | TA | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(276): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.258+1363dupA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr21 | 36710605 | |||||
chr21:36710605
|
T | TAA | 21 | a0001c0001t0004g0084a0001c0001t0013g0328a0001c0001t0024g0364others(18): Show | 22 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.258+1362_258+1363d others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr21 | 36710605 | |||||
chr21:36710606
|
A | AAT | 4 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0012g0327others(1): Show | 4 | HG01175.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+1357_258+1358i others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr21 | 36710606 | |||||
chr21:36710639
|
A | G | 8 | a0001c0001t0009g0372a0001c0001t0009g0388a0001c0001t0009g0389others(5): Show | 9 | HG00741.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+1389A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36710639 | ||||||
chr21:36710819
|
A | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(301): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.258+1569A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36710819 | ||||||
chr21:36710942
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0018g0287a0001c0012t0052g0288 | 3 | HG01081.hp2 HG01943.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.259-1591G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36710942 | ||||||
chr21:36710961
|
A | T | 1 | a0001c0002t0002g0202 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.259-1572A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36710961 | ||||||
chr21:36711249
|
C | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(301): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.259-1284C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36711249 | ||||||
chr21:36711275
|
C | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(301): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.259-1258C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36711275 | ||||||
chr21:36711337
|
A | G | 4 | a0001c0001t0003g0093a0001c0008t0013g0383a0001c0008t0013g0384others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-1196A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36711337 | ||||||
chr21:36711361
|
T | C | 1 | a0002c0003t0003g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-1172T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36711361 | ||||||
chr21:36711439
|
G | A | 14 | a0001c0001t0003g0093a0001c0001t0009g0372a0001c0001t0009g0388others(11): Show | 15 | HG00741.hp2 HG02559.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-1094G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36711439 | ||||||
chr21:36711690
|
C | A | 1 | a0001c0002t0002g0304 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.259-843C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36711690 | ||||||
chr21:36711946
|
G | T | 1 | a0001c0001t0001g0350 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259-587G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36711946 | ||||||
chr21:36711967
|
T | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(303): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.259-566T>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36711967 | ||||||
chr21:36712379
|
C | T | 1 | a0001c0001t0021g0326 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.259-154C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36712379 | ||||||
chr21:36712465
|
G | C | 3 | a0001c0001t0001g0199a0001c0002t0002g0200a0001c0002t0002g0349 | 3 | HG02615.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.259-68G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36712465 | ||||||
chr21:36712473
|
G | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0280a0001c0001t0001g0286others(24): Show | 30 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.259-60G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 2/10 | chr21 | 36712473 | ||||||
chr21:36712663
|
C | T | 1 | a0002c0003t0003g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.348+41C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36712663 | ||||||
chr21:36712681
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.348+59T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36712681 | ||||||
chr21:36713144
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(251): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.348+522G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36713144 | ||||||
chr21:36713183
|
A | G | 2 | a0001c0004t0015g0346a0001c0004t0015g0347 | 2 | HG01243.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.348+561A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36713183 | ||||||
chr21:36713198
|
C | T | 1 | a0001c0001t0018g0020 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.348+576C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36713198 | ||||||
chr21:36713218
|
G | A | 4 | a0001c0001t0018g0198a0001c0002t0002g0373a0001c0007t0013g0381others(1): Show | 5 | HG02809.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+596G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36713218 | ||||||
chr21:36713442
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(283): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.348+820T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36713442 | ||||||
chr21:36713556
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.348+934T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36713556 | ||||||
chr21:36713971
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(284): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.348+1349G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36713971 | ||||||
chr21:36714011
|
A | T | 3 | a0001c0001t0004g0065a0001c0001t0008g0181a0001c0002t0002g0298 | 3 | HG03017.hp1 HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.348+1389A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36714011 | ||||||
chr21:36714026
|
A | G | 1 | a0001c0002t0002g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.348+1404A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36714026 | ||||||
chr21:36714089
|
A | G | 1 | a0002c0003t0003g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.348+1467A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36714089 | ||||||
chr21:36714094
|
C | T | 4 | a0001c0001t0009g0230a0001c0002t0002g0201a0001c0002t0002g0202others(1): Show | 4 | HG02965.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+1472C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36714094 | ||||||
chr21:36714278
|
A | G | 1 | a0001c0002t0029g0140 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.348+1656A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36714278 | ||||||
chr21:36714394
|
G | A | 5 | a0001c0001t0005g0187a0001c0001t0053g0078a0001c0002t0002g0069others(2): Show | 5 | HG02602.hp2 HG03654.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+1772G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36714394 | ||||||
chr21:36714492
|
T | C | 5 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0009g0203others(2): Show | 5 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+1870T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36714492 | ||||||
chr21:36714629
|
G | A | 1 | a0001c0002t0015g0340 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.348+2007G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36714629 | ||||||
chr21:36714849
|
G | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(283): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.348+2227G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36714849 | ||||||
chr21:36714939
|
A | G | 1 | a0001c0004t0002g0012 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.348+2317A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36714939 | ||||||
chr21:36715186
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0247 | 2 | NA19009.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.348+2564C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36715186 | ||||||
chr21:36715187
|
G | A | 1 | a0001c0002t0002g0143 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.348+2565G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36715187 | ||||||
chr21:36715193
|
C | T | 14 | a0001c0001t0001g0073a0001c0001t0001g0135a0001c0001t0001g0138others(11): Show | 14 | HG00673.hp1 HG02129.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.348+2571C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36715193 | ||||||
chr21:36715278
|
A | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.348+2656A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36715278 | ||||||
chr21:36715341
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(103): Show | 111 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.348+2719A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36715341 | ||||||
chr21:36715352
|
G | A | 9 | a0001c0001t0001g0262a0001c0001t0001g0273a0001c0001t0005g0170others(6): Show | 9 | HG00738.hp1 HG02071.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+2730G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36715352 | ||||||
chr21:36715515
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0280a0001c0001t0001g0286others(13): Show | 18 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(15): Show |
intron_variant | MODIFIER | c.348+2893G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36715515 | ||||||
chr21:36715764
|
A | C | 1 | a0001c0001t0001g0257 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.348+3142A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36715764 | ||||||
chr21:36715904
|
GT | G | 7 | a0001c0001t0018g0198a0001c0001t0037g0354a0001c0001t0049g0362others(4): Show | 8 | HG02622.hp1 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+3292delT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 36715904 | |||||
chr21:36715948
|
A | G | 1 | a0001c0004t0035g0370 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+3326A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36715948 | ||||||
chr21:36716000
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0004g0002a0001c0002t0002g0377others(1): Show | 5 | HG02145.hp2 HG02257.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+3378C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716000 | ||||||
chr21:36716061
|
G | A | 2 | a0001c0001t0001g0066a0002c0003t0003g0281 | 2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.348+3439G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716061 | ||||||
chr21:36716121
|
C | T | 2 | a0002c0003t0003g0225a0002c0003t0003g0232 | 2 | HG01496.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.348+3499C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716121 | ||||||
chr21:36716249
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(210): Show | 220 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.349-3572G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716249 | ||||||
chr21:36716347
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.349-3474T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716347 | ||||||
chr21:36716394
|
AC | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(208): Show | 218 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.349-3426delC | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716394 | ||||||
chr21:36716624
|
A | T | 1 | a0001c0002t0043g0030 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.349-3197A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716624 | ||||||
chr21:36716632
|
A | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(290): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.349-3189A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716632 | ||||||
chr21:36716633
|
C | T | 1 | a0002c0003t0003g0274 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.349-3188C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716633 | ||||||
chr21:36716704
|
A | G | 13 | a0001c0001t0001g0094a0001c0001t0011g0204a0001c0001t0012g0327others(10): Show | 13 | HG00741.hp1 HG01106.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-3117A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716704 | ||||||
chr21:36716796
|
A | G | 66 | a0001c0001t0001g0037a0001c0001t0001g0075a0001c0001t0001g0076others(63): Show | 67 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.349-3025A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716796 | ||||||
chr21:36716860
|
A | AT | 35 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0135others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.349-2947dupT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 36716860 | |||||
chr21:36716860
|
AT | A | 89 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0075others(86): Show | 91 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.349-2947delT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 36716860 | |||||
chr21:36716874
|
T | C | 72 | a0001c0001t0001g0037a0001c0001t0001g0075a0001c0001t0001g0076others(69): Show | 74 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.349-2947T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716874 | ||||||
chr21:36716980
|
T | C | 1 | a0001c0010t0001g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.349-2841T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36716980 | ||||||
chr21:36717051
|
A | T | 2 | a0001c0001t0001g0130a0001c0001t0004g0131 | 2 | NA19011.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.349-2770A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36717051 | ||||||
chr21:36717265
|
A | G | 4 | a0001c0001t0018g0198a0001c0002t0002g0373a0001c0007t0013g0381others(1): Show | 5 | HG02809.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-2556A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36717265 | ||||||
chr21:36717328
|
A | C | 1 | a0001c0001t0004g0018 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.349-2493A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36717328 | ||||||
chr21:36717329
|
A | C | 1 | a0001c0001t0004g0018 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.349-2492A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36717329 | ||||||
chr21:36717450
|
C | CT | 100 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0073others(97): Show | 102 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.349-2356dupT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 36717450 | |||||
chr21:36717579
|
C | T | 21 | a0001c0001t0001g0094a0001c0001t0001g0322a0001c0001t0001g0379others(18): Show | 21 | HG01106.hp2 HG01175.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.349-2242C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36717579 | ||||||
chr21:36717585
|
T | G | 10 | a0001c0001t0001g0002a0001c0001t0004g0002a0001c0002t0002g0374others(7): Show | 11 | HG00639.hp1 HG00741.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.349-2236T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36717585 | ||||||
chr21:36717592
|
C | T | 1 | a0001c0002t0002g0373 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.349-2229C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36717592 | ||||||
chr21:36717860
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(106): Show | 114 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.349-1961T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36717860 | ||||||
chr21:36718010
|
G | T | 2 | a0001c0001t0037g0354a0001c0001t0049g0362 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.349-1811G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718010 | ||||||
chr21:36718130
|
G | A | 8 | a0001c0001t0001g0031a0001c0001t0001g0109a0001c0001t0001g0110others(5): Show | 9 | HG00408.hp1 HG00438.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-1691G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718130 | ||||||
chr21:36718257
|
C | T | 1 | a0004c0022t0021g0063 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.349-1564C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718257 | ||||||
chr21:36718282
|
T | C | 1 | a0002c0003t0003g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.349-1539T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718282 | ||||||
chr21:36718439
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0004g0002a0001c0002t0002g0374others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-1382G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718439 | ||||||
chr21:36718511
|
T | C | 1 | a0001c0001t0004g0248 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.349-1310T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718511 | ||||||
chr21:36718584
|
C | T | 2 | a0001c0001t0001g0324a0002c0003t0003g0048 | 2 | HG00099.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.349-1237C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718584 | ||||||
chr21:36718597
|
C | T | 1 | a0001c0001t0005g0195 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.349-1224C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718597 | ||||||
chr21:36718707
|
T | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(239): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.349-1114T>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718707 | ||||||
chr21:36718768
|
G | T | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.349-1053G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718768 | ||||||
chr21:36718784
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0004g0002a0001c0001t0021g0326others(7): Show | 11 | HG00639.hp1 HG01884.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.349-1037C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718784 | ||||||
chr21:36718846
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.349-975G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718846 | ||||||
chr21:36718913
|
A | C | 1 | a0001c0001t0004g0242 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.349-908A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718913 | ||||||
chr21:36718928
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0246a0001c0001t0001g0260others(7): Show | 11 | HG01074.hp1 HG01081.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-893C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718928 | ||||||
chr21:36718958
|
T | G | 1 | a0001c0018t0040g0146 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349-863T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36718958 | ||||||
chr21:36719059
|
G | A | 19 | a0001c0001t0001g0073a0001c0001t0001g0135a0001c0001t0001g0138others(16): Show | 19 | HG00673.hp1 HG01167.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.349-762G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36719059 | ||||||
chr21:36719230
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(264): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.349-591T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36719230 | ||||||
chr21:36719342
|
C | T | 8 | a0001c0002t0002g0309a0001c0002t0002g0310a0002c0003t0001g0045others(5): Show | 8 | HG01070.hp2 HG01256.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-479C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36719342 | ||||||
chr21:36719388
|
T | C | 3 | a0001c0001t0001g0350a0001c0002t0030g0227a0002c0003t0003g0028 | 3 | HG02735.hp2 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.349-433T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36719388 | ||||||
chr21:36719517
|
G | A | 1 | a0001c0001t0004g0018 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.349-304G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36719517 | ||||||
chr21:36719738
|
A | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(216): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.349-83A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36719738 | ||||||
chr21:36719770
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0004g0002a0001c0002t0002g0377others(2): Show | 6 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-51C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36719770 | ||||||
chr21:36719771
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0061a0001c0001t0001g0073others(9): Show | 13 | HG01109.hp1 HG01255.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-50G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 3/10 | chr21 | 36719771 | ||||||
chr21:36719946
|
G | GA | 21 | a0001c0001t0001g0142a0001c0001t0003g0093a0001c0001t0041g0054others(18): Show | 22 | HG00741.hp1 HG01081.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.457+28dupA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr21 | 36719946 | |||||
chr21:36719946
|
GA | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0075others(30): Show | 35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.457+28delA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr21 | 36719946 | |||||
chr21:36719947
|
A | G | 3 | a0001c0001t0004g0297a0001c0001t0004g0392a0001c0002t0002g0376 | 3 | HG01891.hp1 HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.457+18A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36719947 | ||||||
chr21:36720011
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0004g0002a0001c0002t0002g0377others(2): Show | 6 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+82C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720011 | ||||||
chr21:36720028
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0004g0002a0001c0002t0002g0377others(2): Show | 6 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+99G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720028 | ||||||
chr21:36720079
|
C | A | 1 | a0001c0001t0001g0311 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.457+150C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720079 | ||||||
chr21:36720098
|
T | C | 4 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0021g0326others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+169T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720098 | ||||||
chr21:36720104
|
C | T | 1 | a0001c0001t0007g0355 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.457+175C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720104 | ||||||
chr21:36720156
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.457+227G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720156 | ||||||
chr21:36720399
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(110): Show | 117 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.457+470T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720399 | ||||||
chr21:36720432
|
T | C | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.457+503T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720432 | ||||||
chr21:36720556
|
T | C | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0007g0011others(1): Show | 5 | HG01070.hp1 HG01071.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+627T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720556 | ||||||
chr21:36720585
|
G | A | 1 | a0003c0005t0012g0394 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.457+656G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720585 | ||||||
chr21:36720618
|
T | G | 9 | a0001c0001t0009g0203a0001c0001t0009g0372a0001c0001t0009g0388others(6): Show | 10 | HG01175.hp2 HG01975.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.457+689T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720618 | ||||||
chr21:36720623
|
A | G | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.457+694A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720623 | ||||||
chr21:36720770
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(171): Show | 180 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.457+841T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720770 | ||||||
chr21:36720855
|
G | T | 1 | a0002c0003t0003g0028 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.457+926G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720855 | ||||||
chr21:36720876
|
A | G | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(320): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.457+947A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720876 | ||||||
chr21:36720934
|
C | T | 1 | a0001c0001t0004g0312 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.457+1005C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36720934 | ||||||
chr21:36721072
|
A | G | 1 | a0001c0001t0004g0103 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.457+1143A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721072 | ||||||
chr21:36721159
|
A | C | 1 | a0001c0004t0034g0050 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.457+1230A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721159 | ||||||
chr21:36721296
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.457+1367T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721296 | ||||||
chr21:36721328
|
G | A | 1 | a0001c0001t0008g0171 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.457+1399G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721328 | ||||||
chr21:36721541
|
G | A | 2 | a0001c0001t0041g0054a0001c0002t0002g0313 | 2 | HG00741.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.458-1504G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721541 | ||||||
chr21:36721571
|
G | C | 2 | a0001c0001t0001g0094a0001c0001t0012g0327 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.458-1474G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721571 | ||||||
chr21:36721646
|
C | T | 26 | a0001c0001t0003g0093a0001c0001t0009g0203a0001c0001t0009g0372others(23): Show | 27 | HG00741.hp1 HG01175.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.458-1399C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721646 | ||||||
chr21:36721718
|
G | A | 1 | a0001c0001t0012g0327 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.458-1327G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721718 | ||||||
chr21:36721787
|
C | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0061a0001c0001t0001g0073others(21): Show | 26 | HG00735.hp1 HG01109.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.458-1258C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721787 | ||||||
chr21:36721809
|
C | T | 1 | a0001c0001t0004g0392 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458-1236C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721809 | ||||||
chr21:36721858
|
T | C | 1 | a0001c0001t0021g0326 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.458-1187T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721858 | ||||||
chr21:36721967
|
G | A | 3 | a0001c0014t0002g0378a0002c0003t0003g0038a0002c0003t0003g0356 | 3 | HG01884.hp1 HG03239.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.458-1078G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36721967 | ||||||
chr21:36722044
|
G | A | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.458-1001G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36722044 | ||||||
chr21:36722073
|
G | C | 2 | a0001c0001t0004g0106a0001c0001t0005g0169 | 2 | HG02074.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.458-972G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36722073 | ||||||
chr21:36722248
|
A | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0136a0001c0002t0002g0004others(1): Show | 5 | NA18953.hp1 NA18968.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-797A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36722248 | ||||||
chr21:36722360
|
A | T | 1 | a0002c0003t0003g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.458-685A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36722360 | ||||||
chr21:36722621
|
C | T | 2 | a0002c0003t0014g0352a0002c0003t0014g0353 | 2 | HG00099.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.458-424C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36722621 | ||||||
chr21:36722628
|
G | GTCCT | 22 | a0001c0001t0001g0055a0001c0001t0009g0230a0001c0001t0011g0204others(19): Show | 22 | HG01358.hp2 HG01433.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.458-414_458-411dup others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr21 | 36722628 | |||||
chr21:36722658
|
G | A | 1 | a0001c0001t0008g0155 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.458-387G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36722658 | ||||||
chr21:36722692
|
C | G | 1 | a0001c0001t0004g0103 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.458-353C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36722692 | ||||||
chr21:36722759
|
C | T | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.458-286C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36722759 | ||||||
chr21:36722850
|
A | G | 3 | a0001c0001t0053g0078a0002c0003t0003g0224a0002c0003t0019g0188 | 3 | HG02602.hp2 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.458-195A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36722850 | ||||||
chr21:36722978
|
C | T | 1 | a0002c0003t0003g0285 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.458-67C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36722978 | ||||||
chr21:36723004
|
C | T | 1 | a0002c0003t0003g0276 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.458-41C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 4/10 | chr21 | 36723004 | ||||||
chr21:36723134
|
C | T | 1 | a0001c0001t0005g0169 | 1 | HG02074.hp2 | splice_region_variant&intron_variant | LOW | c.543+4C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36723134 | ||||||
chr21:36723135
|
G | A | 1 | a0001c0002t0032g0019 | 1 | NA20752.hp2 | splice_region_variant&intron_variant | LOW | c.543+5G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36723135 | ||||||
chr21:36723195
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0012g0327 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.543+65G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36723195 | ||||||
chr21:36723215
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.543+85G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36723215 | ||||||
chr21:36723261
|
C | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.543+131C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36723261 | ||||||
chr21:36723277
|
T | C | 3 | a0001c0001t0041g0054a0001c0004t0002g0323a0001c0007t0012g0393 | 3 | HG00741.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.543+147T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36723277 | ||||||
chr21:36723491
|
G | C | 1 | a0001c0001t0004g0088 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.543+361G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36723491 | ||||||
chr21:36723743
|
A | G | 2 | a0001c0001t0001g0272a0001c0001t0001g0311 | 2 | HG03688.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.543+613A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36723743 | ||||||
chr21:36723909
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(102): Show | 109 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.543+779C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36723909 | ||||||
chr21:36724128
|
C | A | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.543+998C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724128 | ||||||
chr21:36724189
|
G | A | 1 | a0001c0001t0018g0020 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.543+1059G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724189 | ||||||
chr21:36724338
|
G | A | 1 | a0001c0001t0013g0328 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.543+1208G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724338 | ||||||
chr21:36724353
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0012g0327 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.543+1223A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724353 | ||||||
chr21:36724353
|
A | T | 3 | a0001c0001t0041g0054a0001c0004t0002g0323a0001c0007t0012g0393 | 3 | HG00741.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.543+1223A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724353 | ||||||
chr21:36724360
|
C | A | 1 | a0002c0003t0003g0281 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.543+1230C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724360 | ||||||
chr21:36724414
|
G | A | 1 | a0003c0005t0012g0371 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.543+1284G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724414 | ||||||
chr21:36724484
|
T | C | 1 | a0001c0001t0027g0046 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.543+1354T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724484 | ||||||
chr21:36724542
|
G | C | 2 | a0001c0002t0002g0374a0003c0005t0011g0090 | 2 | HG01952.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.543+1412G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724542 | ||||||
chr21:36724562
|
A | C | 1 | a0002c0003t0003g0285 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.543+1432A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724562 | ||||||
chr21:36724575
|
G | A | 5 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0002t0020g0150others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+1445G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724575 | ||||||
chr21:36724607
|
A | C | 1 | a0001c0002t0006g0015 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.543+1477A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724607 | ||||||
chr21:36724674
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(105): Show | 112 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.544-1445T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724674 | ||||||
chr21:36724815
|
T | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(156): Show | 165 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.544-1304T>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724815 | ||||||
chr21:36724920
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(169): Show | 178 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.544-1199T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724920 | ||||||
chr21:36724947
|
T | C | 2 | a0001c0002t0017g0091a0001c0002t0017g0092 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.544-1172T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36724947 | ||||||
chr21:36725097
|
G | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.544-1022G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725097 | ||||||
chr21:36725118
|
G | C | 1 | a0002c0003t0003g0303 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.544-1001G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725118 | ||||||
chr21:36725188
|
A | C | 33 | a0001c0001t0001g0055a0001c0001t0001g0199a0001c0001t0009g0230others(30): Show | 34 | HG00741.hp2 HG01358.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.544-931A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725188 | ||||||
chr21:36725200
|
A | G | 33 | a0001c0001t0001g0055a0001c0001t0001g0199a0001c0001t0009g0230others(30): Show | 34 | HG00741.hp2 HG01358.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.544-919A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725200 | ||||||
chr21:36725234
|
C | T | 1 | a0001c0001t0013g0328 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.544-885C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725234 | ||||||
chr21:36725359
|
C | T | 2 | a0001c0002t0002g0139a0001c0002t0006g0006 | 3 | NA18991.hp1 NA19057.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.544-760C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725359 | ||||||
chr21:36725389
|
G | A | 1 | a0001c0001t0009g0372 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.544-730G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725389 | ||||||
chr21:36725404
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.544-715G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725404 | ||||||
chr21:36725706
|
G | A | 1 | a0001c0002t0015g0340 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.544-413G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725706 | ||||||
chr21:36725777
|
T | C | 51 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0075others(48): Show | 52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.544-342T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725777 | ||||||
chr21:36725781
|
C | T | 1 | a0001c0001t0012g0327 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-338C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725781 | ||||||
chr21:36725814
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.544-305T>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725814 | ||||||
chr21:36725817
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.544-302C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725817 | ||||||
chr21:36725964
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.544-155G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36725964 | ||||||
chr21:36726001
|
A | G | 1 | a0001c0001t0004g0103 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.544-118A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36726001 | ||||||
chr21:36726098
|
C | A | 4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0002t0017g0091others(1): Show | 4 | HG02630.hp1 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-21C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 5/10 | chr21 | 36726098 | ||||||
chr21:36726351
|
C | T | 1 | a0001c0004t0034g0050 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.743+33C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36726351 | ||||||
chr21:36726674
|
A | G | 1 | a0002c0003t0003g0281 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.743+356A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36726674 | ||||||
chr21:36726750
|
G | C | 14 | a0001c0001t0003g0093a0001c0004t0002g0052a0001c0004t0002g0053others(11): Show | 14 | HG01243.hp1 HG02486.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.743+432G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36726750 | ||||||
chr21:36726797
|
G | A | 1 | a0001c0001t0008g0171 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.743+479G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36726797 | ||||||
chr21:36726807
|
G | A | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.743+489G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36726807 | ||||||
chr21:36726910
|
G | A | 4 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+592G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36726910 | ||||||
chr21:36726913
|
T | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0094others(76): Show | 82 | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.743+595T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36726913 | ||||||
chr21:36727141
|
G | A | 1 | a0001c0001t0049g0362 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.743+823G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727141 | ||||||
chr21:36727335
|
TA | T | 45 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0199others(42): Show | 46 | HG00741.hp1 HG01175.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.743+1021delA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 36727335 | |||||
chr21:36727408
|
G | T | 21 | a0001c0001t0001g0055a0001c0001t0001g0199a0001c0001t0009g0230others(18): Show | 21 | HG01433.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.743+1090G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727408 | ||||||
chr21:36727441
|
G | T | 1 | a0002c0003t0014g0341 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.743+1123G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727441 | ||||||
chr21:36727569
|
C | T | 1 | a0007c0017t0002g0293 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.743+1251C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727569 | ||||||
chr21:36727570
|
G | A | 1 | a0001c0001t0037g0354 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.743+1252G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727570 | ||||||
chr21:36727595
|
C | T | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.743+1277C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727595 | ||||||
chr21:36727652
|
G | A | 2 | a0001c0001t0048g0361a0001c0002t0002g0010 | 3 | HG01975.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.743+1334G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727652 | ||||||
chr21:36727715
|
G | C | 2 | a0001c0002t0017g0091a0001c0002t0017g0092 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.743+1397G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727715 | ||||||
chr21:36727870
|
TC | T | 21 | a0001c0001t0003g0093a0001c0001t0041g0054a0001c0001t0049g0362others(18): Show | 22 | HG00741.hp1 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.743+1553delC | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727870 | ||||||
chr21:36727871
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.743+1553C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727871 | ||||||
chr21:36727923
|
G | C | 2 | a0001c0001t0001g0094a0001c0001t0012g0327 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.743+1605G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727923 | ||||||
chr21:36727984
|
G | T | 3 | a0001c0001t0001g0322a0001c0001t0001g0379a0001c0001t0012g0113 | 3 | HG02572.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.743+1666G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36727984 | ||||||
chr21:36728006
|
C | G | 20 | a0001c0001t0001g0055a0001c0001t0001g0199a0001c0001t0009g0230others(17): Show | 20 | HG01433.hp2 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.743+1688C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728006 | ||||||
chr21:36728044
|
C | A | 1 | a0001c0001t0037g0354 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.743+1726C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728044 | ||||||
chr21:36728206
|
G | A | 22 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0199others(19): Show | 22 | HG01433.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.743+1888G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728206 | ||||||
chr21:36728432
|
C | G | 1 | a0002c0003t0003g0081 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.743+2114C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728432 | ||||||
chr21:36728456
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.743+2138C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728456 | ||||||
chr21:36728457
|
G | A | 1 | a0001c0002t0002g0139 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.743+2139G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728457 | ||||||
chr21:36728474
|
C | T | 1 | a0001c0002t0023g0165 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.743+2156C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728474 | ||||||
chr21:36728505
|
G | A | 22 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0199others(19): Show | 22 | HG01433.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.743+2187G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728505 | ||||||
chr21:36728550
|
T | C | 1 | a0008c0015t0001g0268 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.743+2232T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728550 | ||||||
chr21:36728551
|
C | A | 1 | a0008c0015t0001g0268 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.743+2233C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728551 | ||||||
chr21:36728791
|
A | G | 7 | a0001c0001t0018g0198a0001c0001t0021g0326a0001c0001t0024g0364others(4): Show | 8 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.744-2254A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728791 | ||||||
chr21:36728961
|
C | T | 1 | a0001c0001t0013g0328 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.744-2084C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728961 | ||||||
chr21:36728965
|
T | C | 2 | a0001c0002t0017g0091a0001c0002t0017g0092 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.744-2080T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36728965 | ||||||
chr21:36729204
|
G | T | 1 | a0001c0002t0002g0375 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.744-1841G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729204 | ||||||
chr21:36729261
|
C | T | 2 | a0001c0001t0048g0361a0001c0002t0002g0010 | 3 | HG01975.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.744-1784C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729261 | ||||||
chr21:36729302
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.744-1743G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729302 | ||||||
chr21:36729367
|
G | T | 4 | a0001c0002t0002g0374a0003c0005t0011g0090a0003c0005t0011g0149others(1): Show | 4 | HG01952.hp1 HG02258.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.744-1678G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729367 | ||||||
chr21:36729392
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.744-1653C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729392 | ||||||
chr21:36729639
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.744-1406C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729639 | ||||||
chr21:36729650
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.744-1395G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729650 | ||||||
chr21:36729677
|
C | T | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.744-1368C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729677 | ||||||
chr21:36729718
|
T | G | 4 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.744-1327T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729718 | ||||||
chr21:36729773
|
T | G | 1 | a0003c0005t0011g0380 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.744-1272T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729773 | ||||||
chr21:36729777
|
C | T | 1 | a0001c0001t0007g0331 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.744-1268C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729777 | ||||||
chr21:36729778
|
G | A | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.744-1267G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729778 | ||||||
chr21:36729817
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0012g0327 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.744-1228G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729817 | ||||||
chr21:36729820
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.744-1225C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729820 | ||||||
chr21:36729833
|
C | T | 1 | a0002c0003t0003g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.744-1212C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729833 | ||||||
chr21:36729853
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.744-1192C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729853 | ||||||
chr21:36729854
|
G | A | 1 | a0001c0001t0024g0364 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.744-1191G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729854 | ||||||
chr21:36729971
|
G | A | 2 | a0002c0003t0003g0225a0002c0003t0003g0232 | 2 | HG01496.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.744-1074G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36729971 | ||||||
chr21:36730199
|
C | T | 2 | a0001c0001t0037g0354a0002c0003t0003g0051 | 2 | HG00639.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.744-846C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730199 | ||||||
chr21:36730205
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0136a0001c0002t0002g0004others(1): Show | 5 | NA18953.hp1 NA18968.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.744-840C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730205 | ||||||
chr21:36730244
|
G | A | 3 | a0001c0001t0004g0047a0001c0001t0004g0106a0001c0001t0005g0169 | 3 | HG02074.hp2 HG02165.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.744-801G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730244 | ||||||
chr21:36730310
|
G | A | 2 | a0001c0001t0048g0361a0001c0002t0002g0010 | 3 | HG01975.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.744-735G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730310 | ||||||
chr21:36730367
|
G | A | 5 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0002t0017g0091others(2): Show | 5 | HG00735.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.744-678G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730367 | ||||||
chr21:36730418
|
C | T | 2 | a0001c0001t0048g0361a0001c0002t0002g0010 | 3 | HG01975.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.744-627C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730418 | ||||||
chr21:36730524
|
T | C | 1 | a0001c0001t0005g0156 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.744-521T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730524 | ||||||
chr21:36730577
|
C | T | 1 | a0002c0003t0003g0281 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.744-468C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730577 | ||||||
chr21:36730603
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.744-442C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730603 | ||||||
chr21:36730779
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.744-266A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730779 | ||||||
chr21:36730879
|
G | A | 1 | a0001c0002t0020g0150 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.744-166G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 6/10 | chr21 | 36730879 | ||||||
chr21:36731166
|
C | T | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.850+15C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731166 | ||||||
chr21:36731226
|
G | A | 1 | a0001c0001t0004g0236 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.850+75G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731226 | ||||||
chr21:36731281
|
C | T | 12 | a0001c0001t0018g0198a0001c0001t0021g0326a0001c0001t0024g0364others(9): Show | 13 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.850+130C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731281 | ||||||
chr21:36731301
|
C | T | 12 | a0001c0001t0018g0198a0001c0001t0021g0326a0001c0001t0024g0364others(9): Show | 13 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.850+150C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731301 | ||||||
chr21:36731303
|
C | T | 1 | a0001c0002t0015g0351 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.850+152C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731303 | ||||||
chr21:36731316
|
G | A | 3 | a0001c0001t0037g0354a0001c0014t0002g0378a0003c0005t0012g0394 | 3 | HG00735.hp1 HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.850+165G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731316 | ||||||
chr21:36731317
|
GCTGCCTG others(17): Show |
G | 3 | a0001c0001t0037g0354a0001c0014t0002g0378a0003c0005t0012g0394 | 3 | HG00735.hp1 HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.850+167_850+190del others(24): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731317 | ||||||
chr21:36731329
|
C | T | 103 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0062others(100): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.850+178C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731329 | ||||||
chr21:36731346
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.850+195C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731346 | ||||||
chr21:36731439
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.850+288G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731439 | ||||||
chr21:36731518
|
T | C | 2 | a0001c0001t0005g0187a0001c0002t0002g0069 | 2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.850+367T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731518 | ||||||
chr21:36731693
|
C | G | 7 | a0001c0001t0009g0203a0001c0001t0009g0372a0001c0001t0009g0388others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.850+542C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731693 | ||||||
chr21:36731755
|
C | T | 11 | a0001c0001t0018g0198a0001c0001t0024g0364a0001c0001t0037g0354others(8): Show | 12 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+604C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731755 | ||||||
chr21:36731772
|
A | G | 1 | a0001c0001t0002g0117 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.850+621A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731772 | ||||||
chr21:36731909
|
G | A | 1 | a0001c0001t0008g0155 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.850+758G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36731909 | ||||||
chr21:36732044
|
G | A | 1 | a0001c0004t0015g0346 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850+893G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732044 | ||||||
chr21:36732102
|
C | T | 2 | a0001c0002t0017g0091a0001c0002t0017g0092 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.850+951C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732102 | ||||||
chr21:36732103
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.850+952G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732103 | ||||||
chr21:36732120
|
T | C | 1 | a0002c0003t0003g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.850+969T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732120 | ||||||
chr21:36732222
|
G | A | 2 | a0001c0001t0004g0065a0001c0001t0008g0181 | 2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.850+1071G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732222 | ||||||
chr21:36732281
|
G | C | 1 | a0001c0001t0004g0047 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850+1130G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732281 | ||||||
chr21:36732437
|
C | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0037others(147): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.850+1286C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732437 | ||||||
chr21:36732520
|
G | A | 7 | a0001c0001t0001g0286a0001c0001t0001g0302a0002c0003t0003g0219others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+1369G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732520 | ||||||
chr21:36732542
|
A | G | 370 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(367): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.850+1391A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732542 | ||||||
chr21:36732597
|
C | T | 4 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+1446C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732597 | ||||||
chr21:36732635
|
G | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | NA18970.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.850+1484G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732635 | ||||||
chr21:36732760
|
C | T | 3 | a0001c0001t0004g0065a0001c0001t0008g0181a0002c0003t0003g0064 | 3 | HG03710.hp2 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.850+1609C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36732760 | ||||||
chr21:36733083
|
C | G | 2 | a0001c0001t0045g0344a0001c0002t0002g0098 | 2 | HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.850+1932C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733083 | ||||||
chr21:36733167
|
G | A | 2 | a0001c0002t0017g0091a0001c0002t0017g0092 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.850+2016G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733167 | ||||||
chr21:36733239
|
T | A | 1 | a0001c0001t0001g0311 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.850+2088T>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733239 | ||||||
chr21:36733258
|
T | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00408.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.850+2107T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733258 | ||||||
chr21:36733560
|
A | AT | 31 | a0001c0001t0001g0036a0001c0001t0001g0073a0001c0001t0001g0077others(28): Show | 32 | HG00621.hp1 HG00741.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.850+2426dupT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36733560 | |||||
chr21:36733560
|
AT | A | 15 | a0001c0001t0001g0055a0001c0001t0001g0100a0001c0001t0018g0020others(12): Show | 16 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.850+2426delT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36733560 | |||||
chr21:36733577
|
T | C | 2 | a0001c0002t0017g0091a0001c0002t0017g0092 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.850+2426T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733577 | ||||||
chr21:36733712
|
A | C | 4 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+2561A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733712 | ||||||
chr21:36733726
|
A | AT | 7 | a0001c0001t0018g0198a0001c0001t0024g0364a0001c0001t0037g0354others(4): Show | 8 | HG00735.hp1 HG00741.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.850+2583dupT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36733726 | |||||
chr21:36733759
|
C | T | 1 | a0001c0001t0013g0328 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.850+2608C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733759 | ||||||
chr21:36733761
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0037others(144): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.850+2610C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733761 | ||||||
chr21:36733803
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.850+2652C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733803 | ||||||
chr21:36733813
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.850+2662G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733813 | ||||||
chr21:36733908
|
C | T | 69 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0062others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.850+2757C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733908 | ||||||
chr21:36733964
|
C | A | 1 | a0001c0001t0008g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.850+2813C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36733964 | ||||||
chr21:36734011
|
G | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(118): Show | 124 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.850+2860G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734011 | ||||||
chr21:36734043
|
CAG | C | 18 | a0001c0001t0001g0062a0001c0001t0001g0122a0001c0001t0001g0124others(15): Show | 18 | HG00438.hp2 HG00558.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.850+2893_850+2894d others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734043 | ||||||
chr21:36734143
|
A | G | 1 | a0001c0002t0002g0010 | 2 | HG01975.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.850+2992A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734143 | ||||||
chr21:36734242
|
A | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(271): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.850+3091A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734242 | ||||||
chr21:36734267
|
A | G | 1 | a0003c0005t0011g0380 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.850+3116A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734267 | ||||||
chr21:36734316
|
C | A | 1 | a0001c0001t0001g0247 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.850+3165C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734316 | ||||||
chr21:36734365
|
G | A | 4 | a0001c0001t0001g0094a0001c0001t0012g0327a0001c0014t0002g0378others(1): Show | 4 | HG00639.hp1 HG01884.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+3214G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734365 | ||||||
chr21:36734375
|
A | G | 2 | a0001c0001t0048g0361a0001c0002t0002g0010 | 3 | HG01975.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.850+3224A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734375 | ||||||
chr21:36734436
|
A | G | 2 | a0001c0001t0001g0073a0002c0003t0003g0064 | 2 | HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.850+3285A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734436 | ||||||
chr21:36734492
|
C | A | 3 | a0002c0003t0003g0291a0002c0003t0003g0320a0002c0003t0014g0348 | 3 | HG00738.hp2 HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.850+3341C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734492 | ||||||
chr21:36734531
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.850+3380C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734531 | ||||||
chr21:36734550
|
T | TG | 17 | a0001c0001t0001g0002a0001c0001t0001g0262a0001c0001t0001g0273others(14): Show | 18 | HG00738.hp1 HG01109.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.850+3401dupG | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36734550 | |||||
chr21:36734590
|
C | A | 2 | a0001c0002t0017g0091a0001c0002t0017g0092 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.850+3439C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734590 | ||||||
chr21:36734716
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.850+3565C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734716 | ||||||
chr21:36734756
|
T | A | 1 | a0001c0001t0001g0250 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.850+3605T>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734756 | ||||||
chr21:36734821
|
C | T | 2 | a0001c0001t0004g0106a0001c0001t0005g0169 | 2 | HG02074.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.850+3670C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734821 | ||||||
chr21:36734978
|
C | T | 1 | a0001c0002t0002g0003 | 2 | NA18997.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.850+3827C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36734978 | ||||||
chr21:36735005
|
G | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(144): Show | 151 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.850+3854G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735005 | ||||||
chr21:36735009
|
G | C | 2 | a0001c0002t0017g0091a0001c0002t0017g0092 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.850+3858G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735009 | ||||||
chr21:36735037
|
T | C | 1 | a0001c0001t0004g0325 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.850+3886T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735037 | ||||||
chr21:36735046
|
C | T | 2 | a0001c0001t0003g0147a0001c0001t0003g0148 | 2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.850+3895C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735046 | ||||||
chr21:36735057
|
C | T | 1 | a0001c0001t0004g0248 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.850+3906C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735057 | ||||||
chr21:36735070
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0302 | 2 | HG00140.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.850+3919C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735070 | ||||||
chr21:36735141
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.850+3990C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735141 | ||||||
chr21:36735202
|
A | G | 2 | a0001c0001t0048g0361a0001c0002t0002g0010 | 3 | HG01975.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.850+4051A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735202 | ||||||
chr21:36735316
|
G | C | 396 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(393): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.850+4165G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735316 | ||||||
chr21:36735398
|
G | A | 2 | a0001c0002t0017g0091a0001c0002t0017g0092 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.850+4247G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735398 | ||||||
chr21:36735404
|
T | C | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0022others(314): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.850+4253T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735404 | ||||||
chr21:36735521
|
C | A | 1 | a0001c0001t0024g0364 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.850+4370C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735521 | ||||||
chr21:36735558
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0055others(95): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.850+4407T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735558 | ||||||
chr21:36735574
|
G | GC | 396 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(393): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.850+4424dupC | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36735574 | |||||
chr21:36735686
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.850+4535G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735686 | ||||||
chr21:36735753
|
C | T | 1 | a0001c0002t0020g0283 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.850+4602C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735753 | ||||||
chr21:36735891
|
C | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0262a0001c0001t0001g0322others(13): Show | 17 | HG00738.hp1 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.850+4740C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36735891 | ||||||
chr21:36736055
|
C | T | 15 | a0001c0001t0007g0355a0001c0001t0011g0204a0001c0001t0049g0362others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.850+4904C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736055 | ||||||
chr21:36736074
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0018g0198 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.850+4923C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736074 | ||||||
chr21:36736117
|
A | G | 2 | a0001c0001t0049g0362a0003c0005t0012g0371 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.850+4966A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736117 | ||||||
chr21:36736162
|
C | T | 45 | a0001c0001t0001g0089a0001c0001t0001g0199a0001c0001t0001g0254others(42): Show | 45 | HG00280.hp1 HG00408.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.850+5011C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736162 | ||||||
chr21:36736186
|
T | C | 8 | a0001c0001t0012g0327a0001c0001t0013g0328a0001c0002t0002g0366others(5): Show | 9 | HG01106.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.850+5035T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736186 | ||||||
chr21:36736319
|
C | T | 1 | a0001c0001t0004g0103 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.850+5168C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736319 | ||||||
chr21:36736391
|
T | C | 1 | a0001c0001t0041g0054 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850+5240T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736391 | ||||||
chr21:36736406
|
G | A | 78 | a0001c0001t0001g0126a0001c0001t0001g0199a0001c0001t0001g0322others(75): Show | 79 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.850+5255G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736406 | ||||||
chr21:36736407
|
C | T | 7 | a0001c0001t0037g0354a0001c0001t0049g0362a0001c0008t0013g0383others(4): Show | 7 | HG00735.hp1 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.850+5256C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736407 | ||||||
chr21:36736417
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.850+5266C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736417 | ||||||
chr21:36736428
|
A | C | 1 | a0001c0001t0005g0168 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.850+5277A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736428 | ||||||
chr21:36736473
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.851-5244G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736473 | ||||||
chr21:36736475
|
G | A | 3 | a0001c0001t0048g0361a0001c0002t0044g0316a0001c0014t0002g0378 | 3 | HG01884.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.851-5242G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736475 | ||||||
chr21:36736531
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0280 | 4 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-5186G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736531 | ||||||
chr21:36736604
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.851-5113C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736604 | ||||||
chr21:36736731
|
T | TCCTTC | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.851-4976_851-4972d others(7): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736731 | |||||
chr21:36736746
|
T | C | 41 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0254others(38): Show | 44 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.851-4971T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736746 | ||||||
chr21:36736747
|
C | CCTTTCCT others(52): Show |
1 | a0001c0001t0004g0103 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.851-4935_851-4877d others(61): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736747 | |||||
chr21:36736752
|
CCTCCCTC others(47): Show |
C | 1 | a0001c0001t0048g0361 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.851-4962_851-4909d others(56): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736752 | |||||
chr21:36736753
|
C | CT | 38 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0254others(35): Show | 41 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.851-4963dupT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736753 | |||||
chr21:36736755
|
C | T | 38 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0254others(35): Show | 41 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.851-4962C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736755 | ||||||
chr21:36736771
|
T | C | 1 | a0002c0003t0003g0317 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.851-4946T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736771 | ||||||
chr21:36736780
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(239): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.851-4937C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736780 | ||||||
chr21:36736781
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(239): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.851-4936T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736781 | ||||||
chr21:36736782
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(239): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.851-4935T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736782 | ||||||
chr21:36736786
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(239): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.851-4931C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736786 | ||||||
chr21:36736789
|
CTTTCTT | C | 38 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0254others(35): Show | 41 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.851-4920_851-4915d others(8): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736789 | |||||
chr21:36736795
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(239): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.851-4922T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736795 | ||||||
chr21:36736795
|
T | TTCTC | 23 | a0001c0001t0001g0199a0001c0001t0003g0093a0001c0001t0003g0147others(20): Show | 24 | HG01952.hp1 HG01975.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.851-4921_851-4920i others(6): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736795 | |||||
chr21:36736834
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0280a0001c0001t0007g0334others(1): Show | 5 | HG01255.hp1 HG01346.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-4883T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736834 | ||||||
chr21:36736835
|
CTTTCTCT others(10): Show |
C | 1 | a0001c0001t0001g0261 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.851-4880_851-4864d others(19): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736835 | |||||
chr21:36736837
|
TTCTC | T | 36 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0254others(33): Show | 39 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.851-4878_851-4875d others(6): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736837 | |||||
chr21:36736839
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.851-4878C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736839 | ||||||
chr21:36736845
|
CTTTTCTT others(7): Show |
C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(240): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.851-4855_851-4842d others(16): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736845 | |||||
chr21:36736846
|
TTTTCTTT others(11): Show |
T | 1 | a0001c0001t0005g0194 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.851-4856_851-4839d others(20): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736846 | |||||
chr21:36736847
|
T | TTCTGTCT others(20): Show |
3 | a0001c0001t0041g0054a0001c0004t0002g0323a0001c0007t0012g0393 | 3 | HG00741.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.851-4869_851-4868i others(29): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36736847 | |||||
chr21:36736859
|
T | TCTTTC | 3 | a0001c0001t0041g0054a0001c0004t0002g0323a0001c0007t0012g0393 | 3 | HG00741.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.851-4858_851-4857i others(7): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736859 | ||||||
chr21:36736859
|
T | TGTCTTTC others(34): Show |
1 | a0001c0001t0001g0231 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.851-4858_851-4857i others(43): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736859 | ||||||
chr21:36736897
|
T | G | 13 | a0001c0001t0001g0199a0001c0001t0009g0203a0001c0001t0009g0372others(10): Show | 13 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.851-4820T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736897 | ||||||
chr21:36736910
|
G | A | 2 | a0001c0001t0001g0076a0002c0003t0003g0218 | 2 | HG01192.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.851-4807G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736910 | ||||||
chr21:36736949
|
C | A | 1 | a0002c0019t0019g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.851-4768C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736949 | ||||||
chr21:36736979
|
T | C | 14 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0073others(11): Show | 14 | HG01109.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.851-4738T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736979 | ||||||
chr21:36736987
|
C | T | 14 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0073others(11): Show | 14 | HG01109.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.851-4730C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36736987 | ||||||
chr21:36737177
|
T | C | 3 | a0001c0001t0001g0257a0001c0002t0002g0229a0001c0004t0034g0050 | 3 | HG02895.hp2 NA18970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.851-4540T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737177 | ||||||
chr21:36737183
|
C | T | 9 | a0001c0001t0009g0203a0001c0001t0009g0230a0001c0001t0009g0372others(6): Show | 9 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-4534C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737183 | ||||||
chr21:36737251
|
G | A | 5 | a0001c0001t0003g0093a0001c0001t0003g0147a0001c0001t0003g0148others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-4466G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737251 | ||||||
chr21:36737300
|
C | T | 1 | a0001c0001t0024g0364 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.851-4417C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737300 | ||||||
chr21:36737379
|
C | T | 10 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0001g0196others(7): Show | 10 | HG01109.hp1 HG01358.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.851-4338C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737379 | ||||||
chr21:36737381
|
G | C | 5 | a0001c0001t0003g0093a0001c0001t0003g0147a0001c0001t0003g0148others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-4336G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737381 | ||||||
chr21:36737424
|
G | C | 2 | a0001c0002t0002g0206a0001c0002t0002g0207 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.851-4293G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737424 | ||||||
chr21:36737468
|
G | A | 2 | a0001c0001t0012g0327a0003c0005t0012g0394 | 2 | HG00735.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.851-4249G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737468 | ||||||
chr21:36737472
|
G | A | 2 | a0001c0001t0001g0073a0001c0002t0002g0252 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.851-4245G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737472 | ||||||
chr21:36737472
|
G | T | 1 | a0002c0003t0003g0083 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.851-4245G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737472 | ||||||
chr21:36737557
|
A | G | 1 | a0001c0002t0002g0298 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.851-4160A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737557 | ||||||
chr21:36737619
|
C | T | 1 | a0001c0021t0005g0358 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.851-4098C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737619 | ||||||
chr21:36737647
|
A | T | 1 | a0001c0001t0013g0328 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.851-4070A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737647 | ||||||
chr21:36737680
|
G | A | 1 | a0001c0004t0002g0012 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.851-4037G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737680 | ||||||
chr21:36737684
|
T | C | 11 | a0001c0001t0002g0117a0001c0001t0004g0027a0001c0001t0004g0074others(8): Show | 11 | HG00621.hp2 HG02040.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.851-4033T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737684 | ||||||
chr21:36737693
|
A | G | 51 | a0001c0001t0001g0008a0001c0001t0001g0239a0001c0001t0001g0240others(48): Show | 53 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.851-4024A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737693 | ||||||
chr21:36737769
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.851-3948G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737769 | ||||||
chr21:36737817
|
C | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0086a0001c0001t0001g0318others(3): Show | 6 | HG00639.hp2 HG01358.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.851-3900C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737817 | ||||||
chr21:36737869
|
G | T | 99 | a0001c0001t0001g0311a0001c0001t0002g0117a0001c0001t0004g0018others(96): Show | 102 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.851-3848G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737869 | ||||||
chr21:36737946
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.851-3771A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737946 | ||||||
chr21:36737961
|
C | CA | 51 | a0001c0001t0001g0031a0001c0001t0001g0055a0001c0001t0001g0094others(48): Show | 54 | HG00597.hp1 HG01168.hp1 HG01169.hp2 others(51): Show |
intron_variant | MODIFIER | c.851-3735dupA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAA | 9 | a0001c0001t0001g0272a0001c0001t0018g0020a0001c0002t0002g0295others(6): Show | 9 | HG00741.hp2 HG01515.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-3736_851-3735d others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA | 42 | a0001c0001t0001g0199a0001c0001t0007g0334a0001c0001t0007g0335others(39): Show | 42 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.851-3741_851-3735d others(9): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0008a0001c0001t0001g0280a0001c0001t0001g0286others(11): Show | 15 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.851-3742_851-3735d others(10): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(3): Show |
6 | a0001c0002t0017g0091a0001c0002t0017g0092a0001c0008t0013g0384others(3): Show | 6 | HG01516.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-3744_851-3735d others(12): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0003g0093a0001c0001t0003g0148a0001c0007t0013g0381others(3): Show | 6 | HG01123.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-3745_851-3735d others(13): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0003g0147a0001c0007t0003g0024 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.851-3746_851-3735d others(14): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(7): Show |
2 | a0001c0002t0002g0313a0001c0002t0006g0160 | 2 | NA18957.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.851-3748_851-3735d others(16): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(10): Show |
3 | a0001c0002t0002g0208a0001c0002t0002g0234a0001c0002t0032g0019 | 3 | HG01123.hp1 NA18987.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.851-3751_851-3735d others(19): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(11): Show |
2 | a0001c0002t0002g0211a0001c0002t0002g0233 | 2 | HG01256.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.851-3752_851-3735d others(20): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(12): Show |
12 | a0001c0001t0004g0018a0001c0001t0004g0047a0001c0001t0004g0103others(9): Show | 12 | HG02015.hp2 HG02080.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.851-3753_851-3735d others(21): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(13): Show |
12 | a0001c0001t0004g0027a0001c0001t0004g0035a0001c0001t0004g0074others(9): Show | 12 | HG00621.hp2 HG00673.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.851-3754_851-3735d others(22): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(14): Show |
16 | a0001c0001t0002g0117a0001c0001t0004g0065a0001c0001t0004g0236others(13): Show | 16 | HG01070.hp2 HG02080.hp2 HG03225.hp1 others(13): Show |
intron_variant | MODIFIER | c.851-3755_851-3735d others(23): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(15): Show |
13 | a0001c0001t0004g0102a0001c0001t0004g0321a0001c0001t0021g0326others(10): Show | 13 | HG00280.hp1 HG01175.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.851-3735_851-3734i others(24): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(16): Show |
15 | a0001c0001t0004g0088a0001c0001t0004g0105a0001c0002t0002g0004others(12): Show | 16 | HG00621.hp1 HG00735.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.851-3735_851-3734i others(25): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(17): Show |
9 | a0001c0001t0004g0279a0001c0002t0002g0056a0001c0002t0002g0058others(6): Show | 9 | HG01106.hp1 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-3735_851-3734i others(26): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(18): Show |
3 | a0001c0001t0004g0297a0001c0001t0004g0325a0001c0002t0006g0007 | 4 | HG01069.hp2 HG01071.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-3735_851-3734i others(27): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(19): Show |
2 | a0001c0002t0002g0252a0001c0002t0002g0292 | 2 | HG04228.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.851-3735_851-3734i others(28): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(20): Show |
2 | a0001c0002t0002g0087a0001c0002t0002g0267 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.851-3735_851-3734i others(29): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737961
|
C | CAAAAAAA others(27): Show |
1 | a0001c0002t0047g0120 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.851-3735_851-3734i others(36): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737961 | |||||
chr21:36737972
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.851-3735_851-3724d others(14): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737972 | |||||
chr21:36737973
|
A | AAAAAAAA others(5): Show |
1 | a0002c0003t0003g0282 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.851-3735_851-3734i others(14): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737973 | |||||
chr21:36737973
|
A | AAAAAAAA others(4): Show |
8 | a0001c0001t0001g0073a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG01358.hp2 HG01433.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.851-3727_851-3717d others(13): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737973 | |||||
chr21:36737973
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.851-3727_851-3717d others(13): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737973 | |||||
chr21:36737982
|
A | G | 1 | a0002c0003t0003g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.851-3735A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737982 | ||||||
chr21:36737983
|
G | C | 1 | a0002c0003t0003g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.851-3734G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737983 | ||||||
chr21:36737984
|
C | A | 1 | a0002c0003t0003g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.851-3733C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36737984 | ||||||
chr21:36737984
|
C | CA | 54 | a0001c0001t0001g0008a0001c0001t0001g0239a0001c0001t0001g0240others(51): Show | 56 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.851-3724dupA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36737984 | |||||
chr21:36738002
|
A | C | 6 | a0001c0001t0013g0328a0001c0002t0002g0374a0003c0005t0011g0090others(3): Show | 6 | HG01106.hp2 HG01952.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-3715A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738002 | ||||||
chr21:36738018
|
A | C | 1 | a0001c0001t0007g0342 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.851-3699A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738018 | ||||||
chr21:36738039
|
G | C | 13 | a0001c0001t0001g0199a0001c0001t0009g0203a0001c0001t0009g0230others(10): Show | 13 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.851-3678G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738039 | ||||||
chr21:36738090
|
A | G | 1 | a0001c0001t0005g0169 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.851-3627A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738090 | ||||||
chr21:36738333
|
C | T | 2 | a0001c0001t0004g0251a0001c0002t0002g0313 | 2 | HG00673.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.851-3384C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738333 | ||||||
chr21:36738361
|
C | T | 1 | a0001c0001t0004g0108 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.851-3356C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738361 | ||||||
chr21:36738550
|
C | A | 1 | a0002c0003t0003g0317 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.851-3167C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738550 | ||||||
chr21:36738837
|
G | C | 189 | a0001c0001t0001g0008a0001c0001t0001g0199a0001c0001t0001g0239others(186): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.851-2880G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738837 | ||||||
chr21:36738849
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.851-2868G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738849 | ||||||
chr21:36738942
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0005g0194 | 2 | HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.851-2775G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738942 | ||||||
chr21:36738983
|
G | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0280a0001c0001t0007g0334others(1): Show | 5 | HG01255.hp1 HG01346.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-2734G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36738983 | ||||||
chr21:36739060
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.851-2657C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36739060 | ||||||
chr21:36739077
|
ACCT | A | 59 | a0001c0001t0001g0008a0001c0001t0001g0239a0001c0001t0001g0240others(56): Show | 61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.851-2632_851-2630d others(5): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36739077 | |||||
chr21:36739198
|
A | G | 1 | a0001c0001t0024g0364 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.851-2519A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36739198 | ||||||
chr21:36739226
|
T | G | 3 | a0001c0001t0041g0054a0001c0004t0002g0323a0001c0007t0012g0393 | 3 | HG00741.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.851-2491T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36739226 | ||||||
chr21:36739759
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.851-1958C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36739759 | ||||||
chr21:36739828
|
T | C | 3 | a0001c0001t0041g0054a0001c0004t0002g0323a0001c0007t0012g0393 | 3 | HG00741.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.851-1889T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36739828 | ||||||
chr21:36739906
|
C | CAG | 232 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0094others(229): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.851-1810_851-1809d others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36739906 | |||||
chr21:36739919
|
G | A | 111 | a0001c0001t0001g0265a0001c0001t0001g0296a0001c0001t0002g0117others(108): Show | 113 | HG00280.hp1 HG00558.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.851-1798G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36739919 | ||||||
chr21:36739983
|
G | C | 1 | a0001c0001t0001g0205 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.851-1734G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36739983 | ||||||
chr21:36740005
|
A | G | 1 | a0001c0007t0012g0393 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.851-1712A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36740005 | ||||||
chr21:36740009
|
G | A | 3 | a0001c0001t0002g0117a0001c0001t0009g0230a0001c0007t0012g0393 | 3 | HG02965.hp2 HG03041.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.851-1708G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36740009 | ||||||
chr21:36740009
|
G | GAGAA | 45 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0116others(42): Show | 47 | HG00408.hp1 HG00673.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.851-1660_851-1657d others(6): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740009
|
G | GAGAAAGA others(1): Show |
31 | a0001c0001t0001g0115a0001c0001t0001g0126a0001c0001t0001g0128others(28): Show | 31 | HG00099.hp2 HG01099.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.851-1664_851-1657d others(10): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740009
|
G | GAGAAAGA others(5): Show |
9 | a0001c0001t0001g0209a0001c0001t0004g0248a0001c0001t0004g0325others(6): Show | 9 | HG02145.hp1 HG02148.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-1668_851-1657d others(14): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740009
|
G | GAGAAAGA others(9): Show |
1 | a0001c0004t0034g0050 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.851-1672_851-1657d others(18): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740009
|
G | GAGAAAGA others(13): Show |
1 | a0001c0001t0004g0279 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.851-1676_851-1657d others(22): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740009
|
GAGAA | G | 57 | a0001c0001t0001g0025a0001c0001t0001g0070a0001c0001t0001g0073others(54): Show | 58 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.851-1660_851-1657d others(6): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740009
|
GAGAAAGA others(1): Show |
G | 53 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0039others(50): Show | 56 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.851-1664_851-1657d others(10): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740009
|
GAGAAAGA others(5): Show |
G | 35 | a0001c0001t0001g0023a0001c0001t0001g0055a0001c0001t0001g0067others(32): Show | 36 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.851-1668_851-1657d others(14): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740009
|
GAGAAAGA others(9): Show |
G | 51 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0239others(48): Show | 53 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.851-1672_851-1657d others(18): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740009
|
GAGAAAGA others(17): Show |
G | 1 | a0001c0001t0007g0335 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.851-1680_851-1657d others(26): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740009
|
GAGAAAGA others(21): Show |
G | 2 | a0002c0003t0003g0317a0002c0019t0019g0182 | 2 | HG02683.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.851-1684_851-1657d others(30): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740009 | |||||
chr21:36740013
|
A | G | 4 | a0001c0001t0001g0136a0001c0001t0001g0379a0001c0002t0002g0049others(1): Show | 4 | HG00735.hp1 HG02572.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-1704A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36740013 | ||||||
chr21:36740055
|
GAA | G | 15 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0062others(12): Show | 15 | HG00544.hp1 HG00558.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.851-1660_851-1659d others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740055 | |||||
chr21:36740059
|
G | GAAAGAA | 5 | a0001c0004t0002g0053a0001c0004t0002g0367a0001c0004t0015g0346others(2): Show | 5 | HG02622.hp1 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-1657_851-1656i others(8): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740059 | |||||
chr21:36740059
|
G | GAAAGAAA others(7): Show |
1 | a0001c0004t0002g0395 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.851-1657_851-1656i others(16): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36740059 | |||||
chr21:36740083
|
T | C | 4 | a0001c0001t0013g0328a0001c0001t0041g0054a0001c0004t0002g0323others(1): Show | 4 | HG00741.hp1 HG01106.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-1634T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36740083 | ||||||
chr21:36740480
|
G | C | 55 | a0001c0001t0001g0008a0001c0001t0001g0239a0001c0001t0001g0240others(52): Show | 57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.851-1237G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36740480 | ||||||
chr21:36740775
|
C | G | 1 | a0001c0001t0013g0328 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.851-942C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36740775 | ||||||
chr21:36740982
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0004g0002 | 3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.851-735C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36740982 | ||||||
chr21:36741000
|
C | T | 1 | a0001c0001t0004g0035 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.851-717C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36741000 | ||||||
chr21:36741089
|
G | C | 1 | a0003c0005t0012g0394 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.851-628G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36741089 | ||||||
chr21:36741213
|
A | G | 1 | a0002c0003t0003g0281 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.851-504A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36741213 | ||||||
chr21:36741214
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.851-503A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36741214 | ||||||
chr21:36741540
|
C | CGT | 11 | a0001c0001t0001g0199a0001c0001t0009g0203a0001c0001t0009g0230others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.851-165_851-164dup others(2): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 36741540 | |||||
chr21:36741578
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.851-139G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36741578 | ||||||
chr21:36741585
|
C | T | 1 | a0004c0022t0021g0063 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.851-132C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36741585 | ||||||
chr21:36741589
|
C | T | 5 | a0001c0001t0001g0254a0001c0001t0001g0322a0001c0001t0001g0379others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-128C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36741589 | ||||||
chr21:36741601
|
G | A | 4 | a0001c0002t0002g0374a0003c0005t0011g0090a0003c0005t0011g0149others(1): Show | 4 | HG01952.hp1 HG02258.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-116G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36741601 | ||||||
chr21:36741647
|
C | T | 1 | a0001c0002t0002g0098 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.851-70C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36741647 | ||||||
chr21:36741697
|
C | A | 185 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0094others(182): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.851-20C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 7/10 | chr21 | 36741697 | ||||||
chr21:36741909
|
C | G | 5 | a0001c0002t0002g0366a0001c0002t0002g0374a0003c0005t0011g0090others(2): Show | 5 | HG01952.hp1 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.998+45C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36741909 | ||||||
chr21:36741959
|
C | T | 1 | a0001c0002t0032g0019 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.998+95C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36741959 | ||||||
chr21:36742001
|
A | AT | 50 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0350others(47): Show | 53 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.998+149dupT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr21 | 36742001 | |||||
chr21:36742031
|
G | T | 1 | a0001c0002t0002g0208 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.998+167G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742031 | ||||||
chr21:36742125
|
C | T | 3 | a0001c0002t0006g0186a0001c0002t0023g0175a0007c0017t0002g0293 | 3 | HG00621.hp1 NA18954.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.998+261C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742125 | ||||||
chr21:36742141
|
A | G | 118 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0001g0094others(115): Show | 124 | HG00280.hp1 HG00558.hp2 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.998+277A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742141 | ||||||
chr21:36742216
|
A | G | 2 | a0001c0018t0040g0146a0003c0005t0012g0394 | 2 | HG00735.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.998+352A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742216 | ||||||
chr21:36742257
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.998+393T>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742257 | ||||||
chr21:36742400
|
C | CT | 22 | a0001c0001t0001g0199a0001c0001t0007g0355a0001c0002t0002g0033others(19): Show | 22 | HG01175.hp2 HG01358.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.998+547dupT | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr21 | 36742400 | |||||
chr21:36742426
|
A | G | 1 | a0001c0002t0023g0175 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.998+562A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742426 | ||||||
chr21:36742426
|
A | T | 1 | a0001c0002t0002g0069 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.998+562A>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742426 | ||||||
chr21:36742462
|
C | T | 2 | a0001c0002t0002g0087a0001c0002t0002g0267 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.998+598C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742462 | ||||||
chr21:36742466
|
GGA | G | 396 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(393): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.998+604_998+605del others(2): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr21 | 36742466 | |||||
chr21:36742565
|
A | G | 1 | a0001c0001t0053g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.998+701A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742565 | ||||||
chr21:36742618
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0004g0002a0001c0001t0045g0344others(1): Show | 5 | HG01099.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.998+754T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742618 | ||||||
chr21:36742669
|
G | C | 238 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0055others(235): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.999-718G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742669 | ||||||
chr21:36742848
|
A | G | 1 | a0004c0006t0004g0387 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.999-539A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36742848 | ||||||
chr21:36743213
|
A | G | 2 | a0001c0001t0041g0054a0001c0007t0012g0393 | 2 | HG00741.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.999-174A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36743213 | ||||||
chr21:36743367
|
G | A | 2 | a0001c0001t0041g0054a0001c0007t0012g0393 | 2 | HG00741.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.999-20G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 8/10 | chr21 | 36743367 | ||||||
chr21:36743607
|
C | T | 1 | a0004c0006t0008g0359 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1167+52C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | chr21 | 36743607 | ||||||
chr21:36743808
|
G | A | 8 | a0001c0001t0003g0093a0001c0001t0003g0147a0001c0001t0003g0148others(5): Show | 8 | HG02280.hp1 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167+253G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | chr21 | 36743808 | ||||||
chr21:36743971
|
G | A | 39 | a0001c0001t0002g0210a0001c0002t0002g0003a0001c0002t0002g0004others(36): Show | 43 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1167+416G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | chr21 | 36743971 | ||||||
chr21:36744175
|
T | C | 5 | a0001c0001t0018g0198a0001c0001t0037g0354a0001c0008t0013g0383others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168-553T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | chr21 | 36744175 | ||||||
chr21:36744274
|
G | T | 1 | a0005c0009t0007g0339 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1168-454G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | chr21 | 36744274 | ||||||
chr21:36744277
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1168-451A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | chr21 | 36744277 | ||||||
chr21:36744310
|
A | AC | 107 | a0001c0001t0002g0210a0001c0001t0041g0054a0001c0002t0002g0003others(104): Show | 115 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(112): Show |
intron_variant | MODIFIER | c.1168-417dupC | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr21 | 36744310 | |||||
chr21:36744311
|
C | CA | 47 | a0001c0001t0001g0002a0001c0001t0001g0112a0001c0001t0001g0196others(44): Show | 49 | HG00621.hp2 HG00741.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1168-400dupA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr21 | 36744311 | |||||
chr21:36744311
|
C | CAA | 21 | a0001c0001t0001g0261a0001c0001t0004g0018a0001c0001t0004g0027others(18): Show | 21 | HG00673.hp2 HG01099.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.1168-401_1168-400d others(4): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr21 | 36744311 | |||||
chr21:36744312
|
A | C | 4 | a0001c0002t0002g0060a0001c0002t0002g0249a0001c0018t0040g0146others(1): Show | 4 | HG00735.hp1 HG01517.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-416A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | chr21 | 36744312 | ||||||
chr21:36744424
|
GAAAGAAA others(7): Show |
G | 25 | a0001c0001t0001g0026a0001c0001t0001g0072a0001c0001t0001g0104others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.1168-292_1168-279d others(16): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr21 | 36744424 | |||||
chr21:36744428
|
GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0005g0180 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1168-292_1168-283d others(12): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr21 | 36744428 | |||||
chr21:36744466
|
GAGAA | G | 182 | a0001c0001t0001g0122a0001c0001t0001g0196a0001c0001t0001g0197others(179): Show | 191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1168-242_1168-239d others(6): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr21 | 36744466 | |||||
chr21:36745204
|
C | T | 105 | a0001c0001t0002g0210a0001c0002t0002g0003a0001c0002t0002g0004others(102): Show | 112 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(109): Show |
intron_variant | MODIFIER | c.1576+68C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745204 | ||||||
chr21:36745235
|
C | G | 1 | a0001c0001t0024g0364 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1576+99C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745235 | ||||||
chr21:36745263
|
C | T | 4 | a0001c0001t0037g0354a0001c0008t0013g0383a0001c0008t0013g0384others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576+127C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745263 | ||||||
chr21:36745281
|
T | C | 3 | a0001c0001t0001g0209a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG01167.hp1 HG01169.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1576+145T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745281 | ||||||
chr21:36745441
|
T | G | 41 | a0001c0001t0001g0265a0001c0001t0001g0296a0001c0001t0002g0117others(38): Show | 41 | HG00621.hp2 HG00673.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.1576+305T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745441 | ||||||
chr21:36745459
|
T | G | 1 | a0001c0002t0043g0030 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1576+323T>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745459 | ||||||
chr21:36745499
|
C | T | 2 | a0001c0001t0038g0133a0001c0010t0001g0152 | 2 | HG00423.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1576+363C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745499 | ||||||
chr21:36745558
|
ATGCCAGT others(8): Show |
A | 5 | a0001c0001t0003g0093a0001c0001t0003g0147a0001c0001t0003g0148others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1576+425_1576+439d others(17): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 36745558 | |||||
chr21:36745574
|
T | C | 3 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386 | 3 | HG02647.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1576+438T>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745574 | ||||||
chr21:36745637
|
C | A | 1 | a0002c0019t0019g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1576+501C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745637 | ||||||
chr21:36745668
|
C | T | 3 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386 | 3 | HG02647.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1576+532C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745668 | ||||||
chr21:36745739
|
C | T | 1 | a0002c0003t0019g0161 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1576+603C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745739 | ||||||
chr21:36745788
|
G | C | 44 | a0002c0003t0003g0028a0002c0003t0003g0029a0002c0003t0003g0032others(41): Show | 44 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1576+652G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745788 | ||||||
chr21:36745813
|
C | T | 1 | a0001c0002t0002g0315 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1576+677C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745813 | ||||||
chr21:36745949
|
C | T | 5 | a0001c0001t0003g0093a0001c0001t0003g0147a0001c0001t0003g0148others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1576+813C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745949 | ||||||
chr21:36745965
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1576+829C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745965 | ||||||
chr21:36745974
|
G | A | 1 | a0001c0001t0041g0054 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1576+838G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36745974 | ||||||
chr21:36746240
|
G | A | 3 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386 | 3 | HG02647.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1576+1104G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746240 | ||||||
chr21:36746291
|
G | A | 3 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386 | 3 | HG02647.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1576+1155G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746291 | ||||||
chr21:36746312
|
C | CA | 111 | a0001c0001t0001g0199a0001c0001t0002g0210a0001c0002t0002g0003others(108): Show | 119 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.1576+1188dupA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 36746312 | |||||
chr21:36746406
|
C | T | 112 | a0001c0001t0001g0199a0001c0001t0002g0210a0001c0002t0002g0003others(109): Show | 120 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1577-1259C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746406 | ||||||
chr21:36746436
|
CCTT | C | 3 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386 | 3 | HG02647.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1577-1226_1577-122 others(7): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 36746436 | |||||
chr21:36746514
|
A | C | 2 | a0001c0018t0040g0146a0003c0005t0012g0394 | 2 | HG00735.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1577-1151A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746514 | ||||||
chr21:36746627
|
A | G | 2 | a0001c0002t0002g0223a0001c0014t0002g0378 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1577-1038A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746627 | ||||||
chr21:36746632
|
G | C | 1 | a0001c0001t0037g0354 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1577-1033G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746632 | ||||||
chr21:36746633
|
G | C | 3 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386 | 3 | HG02647.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1577-1032G>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746633 | ||||||
chr21:36746639
|
A | C | 218 | a0001c0001t0001g0199a0001c0001t0002g0117a0001c0001t0002g0210others(215): Show | 227 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1577-1026A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746639 | ||||||
chr21:36746640
|
C | A | 3 | a0001c0001t0001g0256a0001c0001t0004g0264a0001c0001t0005g0184 | 3 | NA18985.hp2 NA19056.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1577-1025C>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746640 | ||||||
chr21:36746665
|
C | T | 1 | a0001c0001t0004g0251 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1577-1000C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746665 | ||||||
chr21:36746728
|
A | C | 1 | a0004c0006t0008g0359 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1577-937A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36746728 | ||||||
chr21:36747016
|
A | G | 1 | a0001c0014t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1577-649A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36747016 | ||||||
chr21:36747026
|
AAAAC | A | 44 | a0001c0001t0002g0117a0001c0001t0004g0018a0001c0001t0004g0027others(41): Show | 45 | HG00621.hp2 HG00673.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1577-623_1577-620d others(6): Show |
SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 36747026 | |||||
chr21:36747042
|
C | G | 1 | a0001c0002t0002g0252 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1577-623C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36747042 | ||||||
chr21:36747056
|
A | C | 3 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386 | 3 | HG02647.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1577-609A>C | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36747056 | ||||||
chr21:36747096
|
T | TG | 112 | a0001c0001t0001g0199a0001c0001t0002g0210a0001c0002t0002g0003others(109): Show | 120 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1577-568dupG | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 36747096 | |||||
chr21:36747173
|
G | A | 1 | a0001c0021t0005g0358 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1577-492G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36747173 | ||||||
chr21:36747197
|
G | A | 1 | a0001c0002t0030g0227 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1577-468G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36747197 | ||||||
chr21:36747289
|
G | T | 3 | a0001c0008t0013g0383a0001c0008t0013g0384a0001c0008t0013g0386 | 3 | HG02647.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1577-376G>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36747289 | ||||||
chr21:36747343
|
C | CA | 9 | a0001c0001t0001g0055a0001c0001t0001g0260a0001c0001t0004g0065others(6): Show | 9 | HG01175.hp1 HG01978.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1577-308dupA | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 36747343 | |||||
chr21:36747357
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | NA18977.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1577-308A>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36747357 | ||||||
chr21:36747390
|
C | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0271a0001c0001t0018g0287 | 3 | HG01943.hp2 HG02273.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1577-275C>G | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36747390 | ||||||
chr21:36747534
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0300a0001c0001t0005g0158 | 3 | NA18942.hp2 NA18977.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1577-131G>A | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36747534 | ||||||
chr21:36747660
|
C | T | 1 | a0001c0001t0041g0054 | 1 | HG00741.hp1 | splice_region_variant&intron_variant | LOW | c.1577-5C>T | SIM2 | ENSG00000159263.16 | transcript | ENST00000290399.11 | protein_coding | 10/10 | chr21 | 36747660 |