Variant report

Variant	rs73288157
Chromosome Location	chr8:85020814-85020815
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs58325610	1.00[AFR][1000 genomes]
rs58601555	1.00[AFR][1000 genomes]
rs73288182	1.00[AFR][1000 genomes]
rs73300515	1.00[AFR][1000 genomes]
rs73302473	1.00[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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:85020400-85021800	Enhancers	Duodenum Mucosa	Duodenum
2	chr8:85020600-85021200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:85020600-85021400	Enhancers	Fetal Intestine Small	intestine
4	chr8:85020600-85021800	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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