Variant report

Variant	rs73825708
Chromosome Location	chr4:76959146-76959147
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000225846	TF binding region
CXCL11	TF binding region
ENSG00000156219	Chromatin interaction
ENSG00000169248	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs41490646	1.00[AMR][1000 genomes]
rs55647336	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57567974	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59539700	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59610986	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59666396	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73825717	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73825721	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73825725	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73825726	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73825730	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73825731	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73825733	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73825868	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73825877	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73825879	0.86[AFR][1000 genomes];1.00[AMR][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	esv3353539	chr4:76530136-76993859	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv529613	chr4:76654941-77081576	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv1004627	chr4:76793910-76999584	Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	esv19222	chr4:76948569-76977780	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv1802071	chr4:76948817-76972594	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv1815228	chr4:76955027-76959624	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76958200-76972600	Weak transcription	Right Atrium	heart
2	chr4:76958400-76963200	Weak transcription	HUVEC	blood vessel

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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