Variant report

Variant	rs3796167
Chromosome Location	chr3:156114048-156114049
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]
rs3772248	1.00[CHB][hapmap]
rs816547	1.00[CHB][hapmap]

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	nsv1014755	chr3:155889430-156411894	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	esv1806015	chr3:156095513-156114898	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 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	chr3:156108200-156117000	Weak transcription	HSMMtube	muscle
2	chr3:156111200-156161600	Weak transcription	Aorta	Aorta
3	chr3:156113400-156115600	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr3:156113600-156115400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr3:156113600-156115400	Enhancers	Colon Smooth Muscle	Colon
6	chr3:156113600-156115800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:156113800-156114600	Enhancers	Fetal Kidney	kidney
8	chr3:156114000-156115400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:156114000-156115800	Enhancers	NHDF-Ad	bronchial

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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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