Variant report

Variant	rs2079387
Chromosome Location	chr7:7672350-7672351
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10236714	0.82[JPT][hapmap]
rs10250880	0.84[ASN][1000 genomes]
rs11772656	0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs13438316	0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs1557996	1.00[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs16878455	1.00[CHB][hapmap]
rs2051911	0.82[ASN][1000 genomes]
rs2108065	1.00[CHB][hapmap]
rs28579471	0.80[ASN][1000 genomes]
rs2881867	0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs3757528	1.00[CHB][hapmap]
rs3779375	1.00[CHB][hapmap]
rs3807857	1.00[CHB][hapmap]
rs4725006	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6463710	1.00[CHB][hapmap]
rs6948086	0.82[ASN][1000 genomes]
rs6966601	1.00[CHB][hapmap]
rs7777893	0.84[ASN][1000 genomes]
rs7781543	0.84[ASN][1000 genomes]
rs7782245	1.00[CHB][hapmap]
rs7788388	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs7793675	0.84[ASN][1000 genomes]
rs7801325	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949293	chr7:6990891-7711883	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv1026758	chr7:7187491-8075259	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
3	nsv887472	chr7:7405069-7680697	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers 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
4	nsv606042	chr7:7427535-7876466	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv887474	chr7:7519603-7679644	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv887475	chr7:7519603-7679644	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
7	nsv887476	chr7:7519603-7680697	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	nsv887477	chr7:7531819-7810122	Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
9	nsv1032670	chr7:7535515-8017077	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
10	nsv8043	chr7:7589195-7862802	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
11	nsv1034199	chr7:7617835-7691176	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
12	nsv606044	chr7:7652372-7727101	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
13	nsv887478	chr7:7670718-7917360	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7639800-7674600	Weak transcription	A549	lung
2	chr7:7649000-7679000	Weak transcription	HSMM	muscle
3	chr7:7669000-7679000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr7:7670800-7674800	Weak transcription	Primary T cells from cord blood	blood
5	chr7:7671000-7673600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:7671400-7679200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr7:7671600-7674800	Weak transcription	Primary B cells from peripheral blood	blood
8	chr7:7671600-7679200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:7671600-7679200	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr7:7671800-7674600	Weak transcription	Lung	lung
11	chr7:7671800-7674800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:7671800-7678800	Weak transcription	NHDF-Ad	bronchial
13	chr7:7672000-7674800	Weak transcription	Fetal Thymus	thymus
14	chr7:7672000-7675200	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr7:7672000-7675400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:7672000-7675600	Weak transcription	Fetal Intestine Small	intestine
17	chr7:7672000-7679000	Weak transcription	Fetal Intestine Large	intestine
18	chr7:7672000-7679200	Weak transcription	Aorta	Aorta
19	chr7:7672200-7674600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr7:7672200-7674600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:7672200-7675400	Weak transcription	Thymus	Thymus
22	chr7:7672200-7677800	Weak transcription	HepG2	liver
23	chr7:7672200-7679200	Weak transcription	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links