Variant report

Variant	rs60221291
Chromosome Location	chr7:19705033-19705034
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:18630158..18631096-chr7:19704896..19705753,2	MCF-7	breast:
2	chr7:19161360..19162323-chr7:19704757..19705725,5	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs17141796	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2390154	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3735616	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58056591	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58354969	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60983452	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60986520	0.91[AMR][1000 genomes]
rs61052896	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66483938	0.91[AMR][1000 genomes]
rs66857203	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67008311	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67320494	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67480144	0.91[AMR][1000 genomes]
rs67667438	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs67685641	0.82[AMR][1000 genomes]
rs6946719	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73076839	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73270117	0.91[AMR][1000 genomes]
rs73271905	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73271979	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73272001	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73274010	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73274011	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73274016	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73274017	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73274019	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73274023	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73274032	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73274033	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73274035	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73274039	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9690343	0.88[AMR][1000 genomes];1.00[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	nsv1018601	chr7:19272360-20008881	Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
2	nsv1020275	chr7:19677535-19730557	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1033223	chr7:19682192-20461375	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv538795	chr7:19682192-20461375	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19703600-19705200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:19703600-19705200	Enhancers	Muscle Satellite Cultured Cells	--
3	chr7:19703800-19705200	Enhancers	Fetal Stomach	stomach
4	chr7:19704000-19705200	Enhancers	Primary B cells from cord blood	blood
5	chr7:19704000-19705200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:19704600-19705200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:19704600-19707600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr7:19705000-19705200	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr7:19705000-19707600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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