Variant report

Variant	rs1836960
Chromosome Location	chr6:81210081-81210082
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10452562	1.00[EUR][1000 genomes]
rs16891800	1.00[EUR][1000 genomes]
rs4498303	1.00[EUR][1000 genomes]
rs4562096	1.00[EUR][1000 genomes]
rs4583942	1.00[EUR][1000 genomes]
rs56384135	1.00[EUR][1000 genomes]
rs56792199	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57987456	1.00[EUR][1000 genomes]
rs61163277	1.00[EUR][1000 genomes]
rs6454160	1.00[EUR][1000 genomes]
rs6454173	1.00[EUR][1000 genomes]
rs6902405	1.00[EUR][1000 genomes]
rs6928467	1.00[EUR][1000 genomes]
rs6933538	1.00[EUR][1000 genomes]
rs6938082	1.00[EUR][1000 genomes]
rs73471450	1.00[EUR][1000 genomes]
rs73471494	1.00[EUR][1000 genomes]
rs73471501	1.00[EUR][1000 genomes]
rs73473428	1.00[EUR][1000 genomes]
rs73473435	1.00[EUR][1000 genomes]
rs73475610	1.00[EUR][1000 genomes]
rs73748607	1.00[EUR][1000 genomes]
rs73748610	1.00[EUR][1000 genomes]
rs73748616	1.00[EUR][1000 genomes]
rs7747214	1.00[EUR][1000 genomes]
rs7747880	1.00[EUR][1000 genomes]
rs7756784	1.00[EUR][1000 genomes]
rs7768308	1.00[EUR][1000 genomes]
rs7768835	1.00[EUR][1000 genomes]
rs7772770	1.00[EUR][1000 genomes]
rs7773470	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531333	chr6:81042427-81836484	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1019670	chr6:81086504-81569984	ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv915714	chr6:81134888-81366749	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1019932	chr6:81155458-81217868	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv886311	chr6:81166178-81239971	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv886312	chr6:81166178-81309481	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv886313	chr6:81177227-81239971	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81208000-81222600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:81208200-81212200	Weak transcription	Fetal Intestine Small	intestine
3	chr6:81208400-81211200	Weak transcription	Fetal Intestine Large	intestine
4	chr6:81208600-81211600	Weak transcription	HepG2	liver
5	chr6:81208800-81210400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr6:81209000-81210600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:81209600-81210400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr6:81209600-81210400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:81209600-81210400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr6:81209600-81210600	Enhancers	Fetal Heart	heart
11	chr6:81209800-81210200	Enhancers	HUES6 Cell Line	embryonic stem cell

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