Variant report

Variant	rs61149083
Chromosome Location	chr6:81472727-81472728
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10485284	0.91[AFR][1000 genomes]
rs11754366	0.91[AFR][1000 genomes]
rs11755359	0.93[AFR][1000 genomes]
rs11756075	0.91[AFR][1000 genomes]
rs11757791	0.93[AFR][1000 genomes]
rs11759374	0.85[AFR][1000 genomes]
rs12662185	0.92[AFR][1000 genomes]
rs12662485	0.80[AFR][1000 genomes]
rs12662681	0.91[AFR][1000 genomes]
rs12662716	0.91[AFR][1000 genomes]
rs12662746	0.83[AFR][1000 genomes]
rs12663298	0.98[AFR][1000 genomes]
rs13197064	0.93[AFR][1000 genomes]
rs13197173	0.88[AFR][1000 genomes]
rs13197442	0.93[AFR][1000 genomes]
rs13198210	0.88[AFR][1000 genomes]
rs13198536	0.98[AFR][1000 genomes]
rs13201732	0.93[AFR][1000 genomes]
rs13208947	0.91[AFR][1000 genomes]
rs13212232	0.98[AFR][1000 genomes]
rs13219453	0.93[AFR][1000 genomes]
rs16892247	0.98[AFR][1000 genomes]
rs17777424	0.93[AFR][1000 genomes]
rs34173535	0.93[AFR][1000 genomes]
rs34192295	0.93[AFR][1000 genomes]
rs34391976	0.93[AFR][1000 genomes]
rs34394883	0.88[AFR][1000 genomes]
rs34504200	0.88[AFR][1000 genomes]
rs34691222	0.93[AFR][1000 genomes]
rs34899637	0.93[AFR][1000 genomes]
rs34957820	0.93[AFR][1000 genomes]
rs35052062	0.88[AFR][1000 genomes]
rs35372769	0.93[AFR][1000 genomes]
rs35520373	0.93[AFR][1000 genomes]
rs4451106	0.91[AFR][1000 genomes]
rs56070062	0.93[AFR][1000 genomes]
rs57763740	0.93[AFR][1000 genomes]
rs58728621	0.93[AFR][1000 genomes]
rs60135513	0.93[AFR][1000 genomes]
rs61367693	0.93[AFR][1000 genomes]
rs66868615	0.93[AFR][1000 genomes]
rs67341284	0.91[AFR][1000 genomes]
rs67738363	0.93[AFR][1000 genomes]
rs6918630	0.91[AFR][1000 genomes]
rs6921328	0.93[AFR][1000 genomes]
rs6934808	0.98[AFR][1000 genomes]
rs6939652	0.91[AFR][1000 genomes]
rs71566924	0.93[AFR][1000 genomes]
rs71566925	0.93[AFR][1000 genomes]
rs73463671	0.80[AFR][1000 genomes]
rs73465709	0.80[AFR][1000 genomes]
rs73465794	0.98[AFR][1000 genomes]
rs73465795	0.98[AFR][1000 genomes]
rs73465800	0.98[AFR][1000 genomes]
rs73468217	0.98[AFR][1000 genomes]
rs73468236	0.98[AFR][1000 genomes]
rs73468238	0.98[AFR][1000 genomes]
rs73468242	0.88[AFR][1000 genomes]
rs73748841	0.93[AFR][1000 genomes]
rs73748842	1.00[AFR][1000 genomes]
rs73748844	0.91[AFR][1000 genomes]
rs73748847	0.95[AFR][1000 genomes]
rs946484	0.93[AFR][1000 genomes]
rs997835	0.88[AFR][1000 genomes]
rs998078	0.88[AFR][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	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	nsv886315	chr6:81352515-81946866	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv886316	chr6:81390313-81554464	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv886317	chr6:81428336-81536597	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv886318	chr6:81447367-81769538	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81472400-81473000	Enhancers	Pancreatic Islets	Pancreatic Islet

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