Variant report

Variant	rs7614868
Chromosome Location	chr3:112526080-112526081
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs13064268	0.81[ASN][1000 genomes]
rs13064475	0.81[ASN][1000 genomes]
rs13064496	0.81[ASN][1000 genomes]
rs1387015	0.98[ASN][1000 genomes]
rs1387021	0.87[ASN][1000 genomes]
rs2399432	0.87[ASN][1000 genomes]
rs6773083	0.87[ASN][1000 genomes]
rs6784658	0.86[ASN][1000 genomes]
rs9809591	0.87[ASN][1000 genomes]
rs9835599	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3329419	chr3:112236688-112620544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv432477	chr3:112390310-112603310	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv877343	chr3:112470586-112597706	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112519200-112526400	Weak transcription	NHDF-Ad	bronchial
2	chr3:112521000-112529800	Weak transcription	A549	lung
3	chr3:112521600-112531600	Weak transcription	Stomach Mucosa	stomach
4	chr3:112522200-112526400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr3:112522200-112526400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr3:112522400-112526200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr3:112523000-112526200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr3:112523000-112526400	Weak transcription	Primary T cells from cord blood	blood
9	chr3:112524400-112528600	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr3:112524800-112528600	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr3:112525400-112526400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr3:112526000-112526800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:112526000-112527600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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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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