Variant report

Variant	rs2190303
Chromosome Location	chr7:71499256-71499257
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10229928	0.95[EUR][1000 genomes]
rs10266409	0.82[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs10280768	0.97[AFR][1000 genomes]
rs17144279	0.83[AFR][1000 genomes]
rs17144283	0.80[AFR][1000 genomes]
rs59254802	0.95[EUR][1000 genomes]
rs59381375	0.95[EUR][1000 genomes]
rs6964123	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73368174	0.95[EUR][1000 genomes]
rs844678	0.86[EUR][1000 genomes]
rs844679	0.99[EUR][1000 genomes]
rs844680	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs844685	0.94[EUR][1000 genomes]
rs844686	0.95[EUR][1000 genomes]
rs844704	0.95[EUR][1000 genomes]
rs844705	0.95[EUR][1000 genomes]
rs844707	0.95[EUR][1000 genomes]
rs844708	0.95[EUR][1000 genomes]
rs844710	0.93[EUR][1000 genomes]
rs844711	0.95[EUR][1000 genomes]
rs844785	0.95[EUR][1000 genomes]
rs844789	0.94[EUR][1000 genomes]
rs844790	0.95[EUR][1000 genomes]
rs844791	0.95[EUR][1000 genomes]
rs844792	0.95[EUR][1000 genomes]
rs844793	0.95[EUR][1000 genomes]
rs844794	0.95[EUR][1000 genomes]
rs844795	0.95[EUR][1000 genomes]
rs844796	0.95[EUR][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	nsv1026896	chr7:71003462-71721516	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1027496	chr7:71162362-71575116	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916220	chr7:71200006-71708048	Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv531372	chr7:71300090-71909517	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	nsv491610	chr7:71422560-71803630	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv831023	chr7:71443549-71588033	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv531373	chr7:71487076-71765613	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv817506	chr7:71488542-71935721	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 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	chr7:71493400-71503600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:71495400-71502400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:71497800-71500400	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr7:71498600-71500000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr7:71498600-71502000	Weak transcription	Fetal Thymus	thymus
6	chr7:71498800-71507000	Weak transcription	Thymus	Thymus
7	chr7:71499000-71500800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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