Variant report

Variant	rs9561880
Chromosome Location	chr13:96147878-96147879
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10219866	0.96[ASN][1000 genomes]
rs11617639	0.94[ASN][1000 genomes]
rs11619150	0.96[ASN][1000 genomes]
rs11843974	0.87[ASN][1000 genomes]
rs12427460	0.86[ASN][1000 genomes]
rs12866697	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12872431	0.96[ASN][1000 genomes]
rs12876693	0.92[ASN][1000 genomes]
rs12876913	0.95[ASN][1000 genomes]
rs1570903	0.95[ASN][1000 genomes]
rs1570904	0.95[ASN][1000 genomes]
rs1890373	0.96[ASN][1000 genomes]
rs4322517	0.96[ASN][1000 genomes]
rs4335657	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4351928	0.85[ASN][1000 genomes]
rs4387474	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4394950	0.87[ASN][1000 genomes]
rs4402421	0.86[ASN][1000 genomes]
rs4403921	0.90[ASN][1000 genomes]
rs4408415	0.83[ASN][1000 genomes]
rs4409957	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4466958	0.95[ASN][1000 genomes]
rs4547209	0.95[ASN][1000 genomes]
rs4564445	0.96[ASN][1000 genomes]
rs4564446	0.93[ASN][1000 genomes]
rs4587819	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4609701	0.96[ASN][1000 genomes]
rs4771917	0.86[ASN][1000 genomes]
rs4773907	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4773908	0.87[ASN][1000 genomes]
rs4773909	0.86[ASN][1000 genomes]
rs4773910	0.95[ASN][1000 genomes]
rs4773911	0.95[ASN][1000 genomes]
rs4773912	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6492792	0.96[ASN][1000 genomes]
rs6492793	0.90[ASN][1000 genomes]
rs6492796	0.96[ASN][1000 genomes]
rs6492797	0.96[ASN][1000 genomes]
rs6492798	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6492799	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7139829	0.87[ASN][1000 genomes]
rs7322391	0.96[ASN][1000 genomes]
rs7326265	0.96[ASN][1000 genomes]
rs7326546	0.96[ASN][1000 genomes]
rs7328468	0.96[ASN][1000 genomes]
rs7332888	0.96[ASN][1000 genomes]
rs7332917	0.96[ASN][1000 genomes]
rs7338647	0.96[ASN][1000 genomes]
rs7489425	0.84[ASN][1000 genomes]
rs7982486	0.96[ASN][1000 genomes]
rs7982563	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7984234	0.96[ASN][1000 genomes]
rs7990054	0.96[ASN][1000 genomes]
rs7992297	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7995104	0.90[ASN][1000 genomes]
rs7995959	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8002444	0.96[ASN][1000 genomes]
rs8002639	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs877960	0.94[ASN][1000 genomes]
rs877961	0.95[ASN][1000 genomes]
rs877962	0.92[ASN][1000 genomes]
rs927786	0.86[ASN][1000 genomes]
rs927787	0.85[ASN][1000 genomes]
rs927788	0.86[ASN][1000 genomes]
rs9302074	0.96[ASN][1000 genomes]
rs9302075	0.87[ASN][1000 genomes]
rs9302076	0.85[ASN][1000 genomes]
rs946228	0.85[ASN][1000 genomes]
rs946231	0.96[ASN][1000 genomes]
rs9516589	0.96[ASN][1000 genomes]
rs9516590	0.96[ASN][1000 genomes]
rs9524982	0.95[ASN][1000 genomes]
rs9524983	0.95[ASN][1000 genomes]
rs9524984	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9524986	0.94[ASN][1000 genomes]
rs9524987	0.92[ASN][1000 genomes]
rs9524988	0.92[ASN][1000 genomes]
rs9524989	0.85[ASN][1000 genomes]
rs9524991	0.84[ASN][1000 genomes]
rs9590285	0.96[ASN][1000 genomes]
rs9590286	0.91[ASN][1000 genomes]
rs9590287	0.94[ASN][1000 genomes]
rs9590288	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043019	chr13:95924585-96152616	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv2752652	chr13:96059024-96181597	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv900933	chr13:96138087-96215289	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96145000-96152600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:96147200-96148800	Weak transcription	Esophagus	oesophagus

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