Variant report

Variant	rs1228971
Chromosome Location	chr7:84104530-84104531
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1014498	0.93[EUR][1000 genomes]
rs1029538	0.93[EUR][1000 genomes]
rs1228897	0.93[EUR][1000 genomes]
rs1228899	0.93[EUR][1000 genomes]
rs1228900	0.91[EUR][1000 genomes]
rs1228902	0.86[EUR][1000 genomes]
rs1228903	0.85[EUR][1000 genomes]
rs1228904	0.92[EUR][1000 genomes]
rs1228905	0.90[EUR][1000 genomes]
rs1228906	0.84[EUR][1000 genomes]
rs1228907	0.94[EUR][1000 genomes]
rs1228908	0.92[EUR][1000 genomes]
rs1228910	0.94[EUR][1000 genomes]
rs1228911	0.95[EUR][1000 genomes]
rs1228914	0.90[EUR][1000 genomes]
rs1228917	0.91[EUR][1000 genomes]
rs1228918	0.92[EUR][1000 genomes]
rs1228920	0.91[EUR][1000 genomes]
rs1228921	0.93[EUR][1000 genomes]
rs1228924	0.93[EUR][1000 genomes]
rs1228925	0.93[EUR][1000 genomes]
rs1228926	0.91[EUR][1000 genomes]
rs1228928	0.93[EUR][1000 genomes]
rs1228932	0.92[EUR][1000 genomes]
rs1228941	0.93[EUR][1000 genomes]
rs1228964	0.86[EUR][1000 genomes]
rs1228967	0.87[EUR][1000 genomes]
rs1228968	0.93[EUR][1000 genomes]
rs1228969	0.94[EUR][1000 genomes]
rs1228972	0.95[EUR][1000 genomes]
rs1228973	0.95[EUR][1000 genomes]
rs1228974	0.93[EUR][1000 genomes]
rs1228975	0.87[EUR][1000 genomes]
rs1228977	0.93[EUR][1000 genomes]
rs1228978	0.93[EUR][1000 genomes]
rs1235296	0.88[CEU][hapmap];0.92[EUR][1000 genomes]
rs2527524	0.93[EUR][1000 genomes]
rs2706910	0.84[EUR][1000 genomes]
rs9690554	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	esv2754468	chr7:83851249-84166749	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv534431	chr7:84001059-84138511	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv949446	chr7:84003501-84763823	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv888634	chr7:84086502-84196258	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv888635	chr7:84086502-84344258	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84098800-84107000	Weak transcription	NHDF-Ad	bronchial

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