Variant report

Variant	rs55751745
Chromosome Location	chr3:133143088-133143089
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:132439632..132442220-chr3:133141166..133143810,2	K562	blood:
2	chr3:132444895..132445778-chr3:133142129..133143849,5	K562	blood:
3	chr3:132440764..132443232-chr3:133142306..133144547,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000248724	Chromatin interaction
ENSG00000113971	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10935062	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10935063	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13073286	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1871356	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1871357	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2086254	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2293601	0.85[EUR][1000 genomes]
rs2370243	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2370244	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28615290	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2887689	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2887690	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4133679	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4286432	0.82[EUR][1000 genomes]
rs4635703	0.82[EUR][1000 genomes]
rs6781120	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6781394	0.88[ASN][1000 genomes]
rs6804296	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7427918	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9820011	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9827245	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9853488	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9858482	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9858615	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9858947	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9877839	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877504	chr3:133122216-133172374	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv591820	chr3:133134361-133143318	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv522281	chr3:133137434-133167363	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1007047	chr3:133137664-133181388	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1006289	chr3:133137664-133186808	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133142200-133144600	Enhancers	Primary B cells from peripheral blood	blood
2	chr3:133142600-133144200	Enhancers	GM12878-XiMat	blood
3	chr3:133142800-133143200	Enhancers	Primary B cells from cord blood	blood
4	chr3:133142800-133143800	Weak transcription	Liver	Liver
5	chr3:133142800-133145200	Weak transcription	Osteobl	bone
6	chr3:133142800-133147000	Weak transcription	Placenta	Placenta
7	chr3:133142800-133147200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:133142800-133147400	Weak transcription	Esophagus	oesophagus
9	chr3:133142800-133151800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr3:133142800-133154000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr3:133143000-133145200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr3:133143000-133145400	Weak transcription	HSMMtube	muscle
13	chr3:133143000-133145800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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