Variant report

Variant	rs812006
Chromosome Location	chr12:63781842-63781843
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:63779288..63781863-chr12:63785380..63788131,2	K562	blood:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1146110	0.88[ASN][1000 genomes]
rs1146115	0.86[ASN][1000 genomes]
rs1146116	0.92[ASN][1000 genomes]
rs1146117	0.94[ASN][1000 genomes]
rs1250671	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1250672	0.94[ASN][1000 genomes]
rs1250675	0.94[ASN][1000 genomes]
rs1250677	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1250680	0.92[ASN][1000 genomes]
rs1251630	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1251764	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1251765	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1251766	0.91[ASN][1000 genomes]
rs1251767	0.91[ASN][1000 genomes]
rs1272078	0.92[ASN][1000 genomes]
rs1733691	0.92[ASN][1000 genomes]
rs1733692	0.85[AMR][1000 genomes]
rs477614	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs477883	0.83[EUR][1000 genomes]
rs488736	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs512936	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs517142	0.94[ASN][1000 genomes]
rs520269	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs531618	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs534886	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs547213	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs566400	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs699623	0.94[ASN][1000 genomes]
rs699624	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs786853	0.93[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs786860	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs805033	0.94[ASN][1000 genomes]
rs810873	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs812546	0.85[ASN][1000 genomes]
rs936147	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046836	chr12:63392391-64377169	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv1035736	chr12:63526274-63920372	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv541510	chr12:63526274-63920372	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1052866	chr12:63562442-63879794	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv541511	chr12:63562442-63879794	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv832439	chr12:63688083-63865226	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1044694	chr12:63746069-63920831	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv2422401	chr12:63778527-64017057	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63778200-63783200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:63781200-63782000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr12:63781200-63782200	Enhancers	Fetal Intestine Large	intestine
4	chr12:63781400-63782200	Enhancers	Fetal Intestine Small	intestine
5	chr12:63781600-63782000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:63781800-63782000	Enhancers	Gastric	stomach
7	chr12:63781800-63784400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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