Variant report

Variant	rs9373347
Chromosome Location	chr6:142779885-142779886
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10484733	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs11155241	0.86[EUR][1000 genomes]
rs11155242	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs11759653	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs12189838	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12190271	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs12197866	0.85[CEU][hapmap];0.89[EUR][1000 genomes]
rs12213892	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs13198644	1.00[EUR][1000 genomes]
rs1329705	0.93[EUR][1000 genomes]
rs1329707	0.90[EUR][1000 genomes]
rs17071756	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs1928528	1.00[EUR][1000 genomes]
rs2294775	0.92[CEU][hapmap];0.83[CHB][hapmap];1.00[EUR][1000 genomes]
rs262117	0.92[EUR][1000 genomes]
rs262120	0.84[EUR][1000 genomes]
rs262130	0.84[EUR][1000 genomes]
rs3817928	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs4304190	1.00[EUR][1000 genomes]
rs643975	0.84[EUR][1000 genomes]
rs6570511	0.92[CEU][hapmap];0.83[CHB][hapmap];0.99[EUR][1000 genomes]
rs6900087	0.92[CEU][hapmap];0.89[EUR][1000 genomes]
rs6900233	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs6901807	0.99[EUR][1000 genomes]
rs6903424	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs6906468	0.99[EUR][1000 genomes]
rs6912639	0.99[EUR][1000 genomes]
rs6922607	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs6925979	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs7756434	0.99[EUR][1000 genomes]
rs7757571	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs7765770	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs7776356	1.00[EUR][1000 genomes]
rs9321870	0.80[EUR][1000 genomes]
rs9403386	0.82[CHB][hapmap]
rs984932	0.87[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142748000-142782600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:142751600-142780000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:142766200-142782800	Weak transcription	NHLF	lung
4	chr6:142773600-142780000	Weak transcription	Fetal Lung	lung
5	chr6:142773800-142780000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:142774600-142780400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:142774800-142780200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr6:142778400-142780200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr6:142779200-142783400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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