Variant report

Variant	rs236776
Chromosome Location	chr4:103086980-103086981
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12640056	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs151364	0.89[AMR][1000 genomes]
rs151385	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs151386	0.84[EUR][1000 genomes]
rs151479	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs151480	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs151481	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs151482	0.89[AMR][1000 genomes]
rs151498	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs151499	0.84[EUR][1000 genomes]
rs17031983	0.85[CHB][hapmap];0.83[JPT][hapmap]
rs173137	0.88[AMR][1000 genomes]
rs173138	0.89[AMR][1000 genomes]
rs180877	0.89[AMR][1000 genomes]
rs189328	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs190223	0.89[AMR][1000 genomes]
rs236745	0.83[AMR][1000 genomes]
rs236761	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs236762	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs236768	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs236769	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs236770	0.84[EUR][1000 genomes]
rs236775	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs236777	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs236778	0.90[EUR][1000 genomes]
rs236779	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs236780	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs236781	0.88[EUR][1000 genomes]
rs238477	0.80[ASN][1000 genomes]
rs238478	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2850374	0.83[JPT][hapmap]
rs6842661	0.85[CHB][hapmap];0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869164	chr4:102483189-103213842	Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv879682	chr4:102859835-103088491	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103084200-103090600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:103085200-103089400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:103085600-103089800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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