Variant report

Variant	rs73294894
Chromosome Location	chr8:85209391-85209392
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:85209341-85209469	HepG2	liver:	n/a	chr8:85209376-85209387

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:85209287..85211713-chr8:85211805..85214280,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000221185	TF binding region

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs16912697	1.00[AMR][1000 genomes]
rs59415044	1.00[AMR][1000 genomes]
rs73291385	1.00[AMR][1000 genomes]
rs73291389	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73291396	1.00[AMR][1000 genomes]
rs73291399	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73293026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73293085	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73293089	1.00[AMR][1000 genomes]
rs73293091	1.00[AMR][1000 genomes]
rs73293096	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73293097	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73293100	1.00[AMR][1000 genomes]
rs73293101	1.00[AMR][1000 genomes]
rs73294897	1.00[AMR][1000 genomes]
rs73294938	1.00[AMR][1000 genomes]
rs73294940	1.00[AMR][1000 genomes]
rs73296724	1.00[AMR][1000 genomes]
rs73296860	1.00[AMR][1000 genomes]
rs73296865	1.00[AMR][1000 genomes]
rs73299826	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73299828	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73299831	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73304840	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73304860	1.00[AMR][1000 genomes]
rs73304870	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73304881	1.00[AMR][1000 genomes]
rs73304882	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73304884	1.00[AMR][1000 genomes]
rs73306919	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73306938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73306940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73306942	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73306944	1.00[AMR][1000 genomes]
rs73306952	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73306956	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73306959	1.00[AMR][1000 genomes]
rs73306964	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2753846	chr8:84637092-85239703	Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv831374	chr8:85103604-85308976	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1842719	chr8:85198548-85268951	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:85203800-85210200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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