Variant report

Variant	rs7845828
Chromosome Location	chr8:96366400-96366401
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10504945	0.98[ASN][1000 genomes]
rs867351	0.85[ASN][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	nsv429930	chr8:96317910-96454743	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3336817	chr8:96366356-96366753	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96365400-96366400	Enhancers	Fetal Intestine Large	intestine
2	chr8:96365600-96366600	Enhancers	Placenta Amnion	Placenta Amnion
3	chr8:96366000-96366400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:96366000-96366800	Enhancers	HSMMtube	muscle
5	chr8:96366200-96366400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:96366400-96366600	Enhancers	Fetal Intestine Small	intestine
7	chr8:96366400-96377000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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