Variant report

Variant	rs395470
Chromosome Location	chr14:56540833-56540834
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]
rs377471	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	esv34106	chr14:56346245-56550642	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56539400-56541000	Enhancers	Ovary	ovary
2	chr14:56539800-56541800	Enhancers	Fetal Stomach	stomach
3	chr14:56540000-56541200	Enhancers	Fetal Lung	lung
4	chr14:56540600-56541000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr14:56540600-56541000	Enhancers	Gastric	stomach
6	chr14:56540600-56541200	Enhancers	Lung	lung
7	chr14:56540600-56541200	Enhancers	Pancreas	Pancrea
8	chr14:56540600-56541200	Enhancers	Spleen	Spleen

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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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