Variant report

Variant	rs2850820
Chromosome Location	chr11:104606938-104606939
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10791723	0.81[ASN][1000 genomes]
rs10791724	0.83[ASN][1000 genomes]
rs10791725	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10895716	0.85[ASN][1000 genomes]
rs10895718	0.81[ASN][1000 genomes]
rs10895723	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10895725	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10895726	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10895727	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11226465	0.88[ASN][1000 genomes]
rs11226470	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11226473	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11226477	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11226478	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11226487	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11226489	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1147027	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1147028	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1147030	0.89[AFR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1147046	0.85[EUR][1000 genomes]
rs1147047	0.85[EUR][1000 genomes]
rs1200648	0.85[EUR][1000 genomes]
rs1201819	0.85[EUR][1000 genomes]
rs12270999	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12271078	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12293362	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12796922	0.86[ASN][1000 genomes]
rs12803940	0.82[ASN][1000 genomes]
rs1893462	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1893463	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1942504	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1942517	0.85[ASN][1000 genomes]
rs1942519	0.85[ASN][1000 genomes]
rs1944525	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1944526	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1944539	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2000730	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2105710	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2155161	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2187130	0.82[ASN][1000 genomes]
rs4393279	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4466799	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4584548	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4755048	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4755049	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6591092	0.85[ASN][1000 genomes]
rs6591093	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7109427	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7122441	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7123412	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7130311	0.85[EUR][1000 genomes]
rs7938134	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7942166	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7945330	0.80[EUR][1000 genomes];0.89[ASN][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	nsv1044271	chr11:104136156-104666252	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1046098	chr11:104207210-105003661	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1054456	chr11:104358924-104805251	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv531430	chr11:104380924-105194452	Genic enhancers Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv832254	chr11:104412769-104607277	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv2761706	chr11:104523335-104634024	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1050346	chr11:104548749-104664665	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104603200-104607200	Weak transcription	Dnd41	blood
2	chr11:104603600-104607400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr11:104605600-104608400	Enhancers	HUVEC	blood vessel
4	chr11:104606200-104607200	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr11:104606800-104607800	Enhancers	Monocytes-CD14+_RO01746	blood

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