Variant report

Variant	rs4134367
Chromosome Location	chr16:80077002-80077003
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12051173	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[JPT][hapmap];0.88[ASN][1000 genomes]
rs12325508	1.00[CHB][hapmap]
rs16944260	1.00[ASN][1000 genomes]
rs16952080	1.00[CHB][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.88[ASN][1000 genomes]
rs16952105	0.96[ASN][1000 genomes]
rs16952121	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16952193	1.00[ASN][1000 genomes]
rs16952202	1.00[ASN][1000 genomes]
rs4888068	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap]
rs4889069	0.88[ASN][1000 genomes]
rs4889078	0.82[ASN][1000 genomes]
rs4889080	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4889082	1.00[ASN][1000 genomes]
rs4889085	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs59263895	0.88[ASN][1000 genomes]
rs73573920	0.96[ASN][1000 genomes]
rs73573922	0.96[ASN][1000 genomes]
rs8063394	1.00[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	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv573294	chr16:80005642-80131944	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr16:80072800-80085200	Weak transcription	Esophagus	oesophagus
2	chr16:80073200-80078000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:80075000-80079600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr16:80075800-80077400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr16:80076000-80078200	Enhancers	Fetal Stomach	stomach
6	chr16:80076000-80079600	Weak transcription	Fetal Intestine Large	intestine
7	chr16:80076400-80081200	Enhancers	Ovary	ovary
8	chr16:80076800-80078200	Enhancers	Stomach Smooth Muscle	stomach

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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