Variant report

Variant	rs7704789
Chromosome Location	chr5:154375937-154375938
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12108907	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56325403	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61430349	0.91[AFR][1000 genomes]
rs6580125	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73807225	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7702533	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7735146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv968117	chr5:154371654-154381973	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
2	nsv883058	chr5:154375465-154432580	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:154373200-154376400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr5:154373200-154376800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr5:154375400-154377800	Enhancers	HUVEC	blood vessel
4	chr5:154375600-154380400	Weak transcription	HepG2	liver

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

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