Variant report

Variant	rs2087971
Chromosome Location	chr11:26612809-26612810
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 112 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs10430934	0.85[ASN][1000 genomes]
rs10767555	0.96[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10767558	0.85[ASN][1000 genomes]
rs10767560	0.85[ASN][1000 genomes]
rs10767564	0.84[ASN][1000 genomes]
rs10767565	0.83[ASN][1000 genomes]
rs10767566	0.83[ASN][1000 genomes]
rs10835009	0.85[ASN][1000 genomes]
rs10835011	0.85[ASN][1000 genomes]
rs10835012	0.84[ASN][1000 genomes]
rs10835013	0.85[ASN][1000 genomes]
rs10835014	0.85[ASN][1000 genomes]
rs10835015	0.85[ASN][1000 genomes]
rs10835018	0.85[ASN][1000 genomes]
rs10835020	0.85[ASN][1000 genomes]
rs10835022	0.85[ASN][1000 genomes]
rs10835023	0.85[ASN][1000 genomes]
rs10835024	0.85[ASN][1000 genomes]
rs10835025	0.86[ASN][1000 genomes]
rs10835026	0.83[ASN][1000 genomes]
rs10835027	0.85[ASN][1000 genomes]
rs10835028	0.85[ASN][1000 genomes]
rs10835029	0.85[ASN][1000 genomes]
rs10835030	0.85[ASN][1000 genomes]
rs10835032	0.82[ASN][1000 genomes]
rs10835033	0.80[ASN][1000 genomes]
rs10835034	0.84[ASN][1000 genomes]
rs10835035	0.84[ASN][1000 genomes]
rs10835036	0.83[ASN][1000 genomes]
rs10835037	0.83[ASN][1000 genomes]
rs10835038	0.81[ASN][1000 genomes]
rs10835039	0.83[ASN][1000 genomes]
rs10835040	0.83[ASN][1000 genomes]
rs10835041	0.83[ASN][1000 genomes]
rs10835044	0.83[ASN][1000 genomes]
rs11029623	0.88[ASN][1000 genomes]
rs11029638	0.83[ASN][1000 genomes]
rs11029645	0.85[ASN][1000 genomes]
rs11029646	0.85[ASN][1000 genomes]
rs11029647	0.85[ASN][1000 genomes]
rs11029648	0.85[ASN][1000 genomes]
rs11029650	0.85[ASN][1000 genomes]
rs11029651	0.85[ASN][1000 genomes]
rs11029654	0.85[ASN][1000 genomes]
rs11029656	0.82[ASN][1000 genomes]
rs11029659	0.82[ASN][1000 genomes]
rs11512173	0.85[ASN][1000 genomes]
rs11529839	0.87[ASN][1000 genomes]
rs12795885	0.81[ASN][1000 genomes]
rs1565760	0.84[ASN][1000 genomes]
rs1567352	0.85[ASN][1000 genomes]
rs1848564	0.88[ASN][1000 genomes]
rs1848565	0.85[ASN][1000 genomes]
rs2029713	0.84[ASN][1000 genomes]
rs2295	0.83[ASN][1000 genomes]
rs2350211	0.87[ASN][1000 genomes]
rs2839797	0.85[ASN][1000 genomes]
rs28403415	0.85[ASN][1000 genomes]
rs35290179	0.82[ASN][1000 genomes]
rs35760232	0.86[ASN][1000 genomes]
rs3937884	0.88[ASN][1000 genomes]
rs4255495	0.82[ASN][1000 genomes]
rs4268466	0.83[ASN][1000 genomes]
rs4288713	0.82[ASN][1000 genomes]
rs4316465	0.81[ASN][1000 genomes]
rs4320913	0.84[ASN][1000 genomes]
rs4396242	0.84[ASN][1000 genomes]
rs4469843	0.84[ASN][1000 genomes]
rs4474389	0.83[ASN][1000 genomes]
rs4480494	0.82[ASN][1000 genomes]
rs4497357	0.83[ASN][1000 genomes]
rs4498947	0.84[ASN][1000 genomes]
rs4551717	0.83[ASN][1000 genomes]
rs4922764	0.83[ASN][1000 genomes]
rs6484220	0.85[ASN][1000 genomes]
rs6484223	0.85[ASN][1000 genomes]
rs6484224	0.81[ASN][1000 genomes]
rs6484225	0.82[ASN][1000 genomes]
rs6484227	0.82[ASN][1000 genomes]
rs6484228	0.82[ASN][1000 genomes]
rs6484229	0.82[ASN][1000 genomes]
rs6484230	0.80[ASN][1000 genomes]
rs6484231	0.81[ASN][1000 genomes]
rs6484232	0.82[ASN][1000 genomes]
rs7106245	0.83[ASN][1000 genomes]
rs7107528	0.83[ASN][1000 genomes]
rs7107869	0.85[ASN][1000 genomes]
rs7112022	0.85[ASN][1000 genomes]
rs7116352	0.89[ASN][1000 genomes]
rs7122563	0.85[ASN][1000 genomes]
rs7124390	0.83[ASN][1000 genomes]
rs7124404	0.83[ASN][1000 genomes]
rs7479072	0.84[ASN][1000 genomes]
rs7925028	0.85[ASN][1000 genomes]
rs7929519	0.84[ASN][1000 genomes]
rs7929611	0.83[ASN][1000 genomes]
rs7932168	0.87[ASN][1000 genomes]
rs7933233	0.84[ASN][1000 genomes]
rs7933405	0.83[ASN][1000 genomes]
rs7938755	0.84[ASN][1000 genomes]
rs7941987	0.84[ASN][1000 genomes]
rs7942467	0.84[ASN][1000 genomes]
rs7942671	0.85[ASN][1000 genomes]
rs7942776	0.83[ASN][1000 genomes]
rs7943086	0.82[ASN][1000 genomes]
rs7943714	0.85[ASN][1000 genomes]
rs7946841	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044544	chr11:26506962-26967285	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1050121	chr11:26532655-26675303	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv540974	chr11:26532655-26675303	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv916187	chr11:26576875-27328603	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv975163	chr11:26609968-26620267	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26600400-26643000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:26603800-26623200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr11:26604000-26623600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:26606800-26614600	Weak transcription	Placenta	Placenta
5	chr11:26607600-26635400	Weak transcription	Adipose Nuclei	Adipose
6	chr11:26609200-26613800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:26610800-26619000	Weak transcription	Fetal Lung	lung

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