Variant report

Variant	rs61876069
Chromosome Location	chr11:23775604-23775605
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs11819925	0.93[EUR][1000 genomes]
rs11820608	0.93[EUR][1000 genomes]
rs11820669	0.93[EUR][1000 genomes]
rs11822638	0.93[EUR][1000 genomes]
rs11825290	0.87[EUR][1000 genomes]
rs11826810	0.91[EUR][1000 genomes]
rs11827258	0.91[EUR][1000 genomes]
rs11827769	0.93[EUR][1000 genomes]
rs11828396	0.87[EUR][1000 genomes]
rs11828544	0.89[EUR][1000 genomes]
rs4265597	0.84[EUR][1000 genomes]
rs4337039	0.93[EUR][1000 genomes]
rs4641473	0.84[EUR][1000 genomes]
rs56725851	0.89[EUR][1000 genomes]
rs57681918	0.93[EUR][1000 genomes]
rs58247909	0.89[EUR][1000 genomes]
rs58471055	0.89[EUR][1000 genomes]
rs58510850	0.89[EUR][1000 genomes]
rs61467820	0.87[EUR][1000 genomes]
rs61699497	0.93[EUR][1000 genomes]
rs61876062	1.00[EUR][1000 genomes]
rs61876063	1.00[EUR][1000 genomes]
rs61876065	0.91[EUR][1000 genomes]
rs61876066	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61876067	0.84[EUR][1000 genomes]
rs61876068	0.84[EUR][1000 genomes]
rs61876070	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61876071	1.00[EUR][1000 genomes]
rs61876074	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61876075	0.89[EUR][1000 genomes]
rs61876076	0.87[EUR][1000 genomes]
rs61876077	0.89[EUR][1000 genomes]
rs61876078	0.89[EUR][1000 genomes]
rs61876079	0.89[EUR][1000 genomes]
rs61876082	0.85[EUR][1000 genomes]
rs61876083	0.89[EUR][1000 genomes]
rs61876084	0.89[EUR][1000 genomes]
rs61876085	0.89[EUR][1000 genomes]
rs61876087	0.89[EUR][1000 genomes]
rs61876110	0.91[EUR][1000 genomes]
rs61876111	0.89[EUR][1000 genomes]
rs61876112	0.89[EUR][1000 genomes]
rs61876114	0.89[EUR][1000 genomes]
rs61876115	0.89[EUR][1000 genomes]
rs61876116	0.89[EUR][1000 genomes]
rs61876117	0.87[EUR][1000 genomes]
rs61876118	0.87[EUR][1000 genomes]
rs7116643	0.87[EUR][1000 genomes]
rs73423725	0.87[EUR][1000 genomes]
rs73439876	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv553757	chr11:23564329-23896729	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv897062	chr11:23687928-24031627	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916840	chr11:23710275-24064119	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv897063	chr11:23723766-23940407	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv897064	chr11:23767292-23859991	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv897065	chr11:23767292-23882931	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23771600-23776600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr11:23772000-23776600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:23772400-23782400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:23775400-23775800	Enhancers	Colon Smooth Muscle	Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links