Variant report

Variant	rs7611697
Chromosome Location	chr3:79212886-79212887
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11922032	1.00[CEU][hapmap]
rs11925014	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11925923	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11928467	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1378635	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1378636	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17016804	1.00[CEU][hapmap]
rs17016815	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17016836	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17336055	0.89[YRI][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17395825	0.89[YRI][hapmap]
rs2124389	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2124390	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2168372	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34673005	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4334606	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4519664	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4532095	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs5016999	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6766824	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6786720	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6791591	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6804495	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6804803	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs716681	1.00[CEU][hapmap]
rs7617560	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs966144	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[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	nsv834745	chr3:79055426-79227937	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 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	chr3:79210600-79216800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:79210600-79219000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr3:79211400-79213200	Enhancers	Fetal Heart	heart
4	chr3:79211400-79216600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:79211400-79216800	Weak transcription	Brain Germinal Matrix	brain
6	chr3:79211800-79217000	Weak transcription	Fetal Brain Female	brain
7	chr3:79212400-79213800	Weak transcription	Fetal Brain Male	brain
8	chr3:79212400-79216400	Weak transcription	Osteobl	bone
9	chr3:79212400-79216600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr3:79212600-79216400	Weak transcription	NHDF-Ad	bronchial

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