Variant report

Variant	rs35721291
Chromosome Location	chr8:96327874-96327875
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs13278690	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96326800-96328200	Enhancers	Brain Anterior Caudate	brain
2	chr8:96327000-96328000	Enhancers	Brain Angular Gyrus	brain
3	chr8:96327000-96328200	Enhancers	Pancreas	Pancrea
4	chr8:96327000-96329800	Enhancers	Brain Substantia Nigra	brain
5	chr8:96327200-96330200	Enhancers	Brain Hippocampus Middle	brain
6	chr8:96327400-96330200	Enhancers	Brain Cingulate Gyrus	brain
7	chr8:96327600-96328000	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr8:96327600-96328200	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr8:96327600-96329000	Enhancers	Brain Germinal Matrix	brain

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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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