Variant report

Variant	rs3784267
Chromosome Location	chr15:43528614-43528615
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11070391	0.89[EUR][1000 genomes]
rs11070396	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11070397	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11070398	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11855754	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12592725	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12899266	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16957511	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1834643	0.92[EUR][1000 genomes]
rs2042742	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2241516	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28756768	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2899077	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2947019	0.91[EUR][1000 genomes]
rs34646108	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3784268	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4924709	0.90[ASN][1000 genomes]
rs494863	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs495286	0.88[EUR][1000 genomes]
rs497138	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs499280	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs530305	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs531850	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs538218	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs540587	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6493078	0.86[ASN][1000 genomes]
rs7174915	0.89[EUR][1000 genomes]
rs7183814	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8027371	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044522	chr15:43115348-43658417	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv1044508	chr15:43270637-43658417	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3784267	CCNDBP1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43523600-43530800	Weak transcription	K562	blood
2	chr15:43524800-43530200	Weak transcription	Adipose Nuclei	Adipose
3	chr15:43527000-43530400	Weak transcription	Esophagus	oesophagus
4	chr15:43528000-43529000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr15:43528000-43531600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr15:43528200-43529000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr15:43528400-43528800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr15:43528400-43529400	Enhancers	Primary B cells from peripheral blood	blood
9	chr15:43528600-43529000	Enhancers	Primary hematopoietic stem cells	blood

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