Variant report

Variant	rs7805266
Chromosome Location	chr7:150891899-150891900
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12533831	0.83[ASN][1000 genomes]
rs12703116	0.95[ASN][1000 genomes]
rs1469550	0.83[ASN][1000 genomes]
rs2435609	0.83[ASN][1000 genomes]
rs2487151	0.83[ASN][1000 genomes]
rs4726003	0.83[ASN][1000 genomes]
rs4726006	0.85[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	esv1821419	chr7:150593315-150974269	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
2	nsv889476	chr7:150729212-150951819	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	120 gene(s)	inside rSNPs	diseases
3	nsv831188	chr7:150735204-150912875	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
4	nsv609034	chr7:150830015-150893629	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150885000-150910000	Weak transcription	Right Atrium	heart
2	chr7:150889600-150893000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr7:150889800-150892600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:150891000-150892000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
5	chr7:150891200-150892000	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr7:150891600-150893800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr7:150891800-150892000	Bivalent Enhancer	Fetal Intestine Small	intestine
8	chr7:150891800-150892800	Enhancers	Adipose Nuclei	Adipose
9	chr7:150891800-150893200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr7:150891800-150893400	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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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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