Variant report

Variant	rs7735712
Chromosome Location	chr5:90141594-90141595
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10514337	0.83[CHB][hapmap]
rs11956622	0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs12655163	0.96[ASN][1000 genomes]
rs12655900	0.84[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs12657829	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs16869117	0.82[CHB][hapmap]
rs16869133	0.83[CHB][hapmap];0.81[ASN][1000 genomes]
rs16869139	0.88[JPT][hapmap];0.86[ASN][1000 genomes]
rs16869140	0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs16869151	0.89[JPT][hapmap];0.88[ASN][1000 genomes]
rs16869163	0.89[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs1983366	0.82[CEU][hapmap];0.89[JPT][hapmap];0.88[ASN][1000 genomes]
rs2366932	0.88[ASN][1000 genomes]
rs2438361	0.82[CEU][hapmap];0.83[CHB][hapmap];0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs2438366	0.82[ASN][1000 genomes]
rs2438375	0.84[ASN][1000 genomes]
rs2438377	0.93[ASN][1000 genomes]
rs2438379	0.82[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs2438380	0.82[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap]
rs2443076	0.82[CEU][hapmap];0.83[CHB][hapmap];0.81[ASN][1000 genomes]
rs2443084	0.96[ASN][1000 genomes]
rs3107223	0.82[CEU][hapmap];0.83[CHB][hapmap];0.81[ASN][1000 genomes]
rs3763073	0.89[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs73771103	0.89[AFR][1000 genomes]
rs879571	0.82[CEU][hapmap];0.83[CHB][hapmap];0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs9764492	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv531965	chr5:89886550-90145002	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
3	nsv882367	chr5:89956991-90209824	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv1015449	chr5:89968626-90219398	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	nsv517049	chr5:90003131-90262475	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90104600-90142000	Weak transcription	Brain Anterior Caudate	brain
2	chr5:90110200-90149600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr5:90112000-90151200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:90112000-90160600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr5:90112000-90175800	Weak transcription	Fetal Brain Female	brain
6	chr5:90112200-90142200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:90127200-90144600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:90137000-90145400	Weak transcription	K562	blood
9	chr5:90137200-90144600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr5:90137400-90148800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr5:90137600-90144600	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr5:90138000-90144400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:90138000-90146000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr5:90138000-90148600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:90138200-90142000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr5:90138800-90142200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:90139600-90141800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr5:90140000-90142200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr5:90141000-90142400	Enhancers	Fetal Brain Male	brain

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