Variant report

Variant	rs67767464
Chromosome Location	chr3:179710124-179710125
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10513766	0.97[EUR][1000 genomes]
rs12054131	0.95[EUR][1000 genomes]
rs2031045	0.95[EUR][1000 genomes]
rs41463648	0.84[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs41513245	0.97[EUR][1000 genomes]
rs55829880	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs55895012	0.85[EUR][1000 genomes]
rs55903935	0.97[EUR][1000 genomes]
rs55952695	0.98[EUR][1000 genomes]
rs55996513	0.95[EUR][1000 genomes]
rs56006824	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56100025	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56116940	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56145741	0.98[EUR][1000 genomes]
rs56273619	0.98[EUR][1000 genomes]
rs56335806	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56362569	0.83[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs57313970	0.97[EUR][1000 genomes]
rs57943546	0.98[EUR][1000 genomes]
rs6443686	0.94[EUR][1000 genomes]
rs66486754	0.95[EUR][1000 genomes]
rs66810269	0.98[EUR][1000 genomes]
rs66906982	0.84[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs66924709	0.84[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs67219312	0.90[EUR][1000 genomes]
rs6771088	0.96[EUR][1000 genomes]
rs6789142	0.95[EUR][1000 genomes]
rs68011865	0.84[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs6804267	0.84[EUR][1000 genomes]
rs6809015	0.97[EUR][1000 genomes]
rs68185071	0.98[EUR][1000 genomes]
rs68188167	0.82[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs73178101	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73180003	1.00[EUR][1000 genomes]
rs73180017	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73180024	1.00[EUR][1000 genomes]
rs73180036	0.97[EUR][1000 genomes]
rs73180045	0.97[EUR][1000 genomes]
rs73180054	0.95[EUR][1000 genomes]
rs73180061	0.94[EUR][1000 genomes]
rs73180081	0.88[EUR][1000 genomes]
rs73180091	0.88[EUR][1000 genomes]
rs73180095	0.88[EUR][1000 genomes]
rs7645574	0.97[EUR][1000 genomes]
rs9290689	0.97[EUR][1000 genomes]
rs9816489	0.96[EUR][1000 genomes]
rs9828328	0.96[EUR][1000 genomes]
rs9844416	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9849079	0.95[EUR][1000 genomes]
rs9855659	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829807	chr3:179527567-179745153	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv829808	chr3:179574614-179754321	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv534210	chr3:179666123-179899347	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1000756	chr3:179672703-179827373	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179689400-179710200	Weak transcription	Fetal Brain Male	brain
2	chr3:179700800-179721000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr3:179703000-179710200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr3:179703800-179725200	Weak transcription	Dnd41	blood
5	chr3:179708600-179710400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr3:179708800-179710400	Enhancers	HMEC	breast
7	chr3:179709200-179710400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:179709200-179710600	Enhancers	Brain Substantia Nigra	brain
9	chr3:179709400-179710200	Weak transcription	Brain Angular Gyrus	brain
10	chr3:179709400-179710800	Enhancers	Brain Hippocampus Middle	brain
11	chr3:179709800-179710400	Enhancers	Brain Anterior Caudate	brain
12	chr3:179709800-179710600	Enhancers	A549	lung

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