Variant report

Variant	rs35211174
Chromosome Location	chr11:36710276-36710277
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:36710108..36712201-chr11:36728263..36730385,2	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10219403	0.87[AFR][1000 genomes]
rs11033700	1.00[AMR][1000 genomes]
rs11033701	1.00[AMR][1000 genomes]
rs11033702	1.00[AMR][1000 genomes]
rs11033704	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11033705	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11033726	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11033738	0.81[AFR][1000 genomes]
rs11033739	0.87[AFR][1000 genomes]
rs11033740	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11033754	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11820706	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11824427	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11825620	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11828016	1.00[AMR][1000 genomes]
rs12271060	1.00[AMR][1000 genomes]
rs12271149	1.00[AMR][1000 genomes]
rs12271279	1.00[AMR][1000 genomes]
rs12271312	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12272928	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12273684	1.00[AMR][1000 genomes]
rs12273796	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12274228	1.00[AMR][1000 genomes]
rs12274720	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12276673	1.00[AMR][1000 genomes]
rs12277745	1.00[AMR][1000 genomes]
rs12277943	0.90[AFR][1000 genomes]
rs12279639	1.00[AMR][1000 genomes]
rs12280515	1.00[AMR][1000 genomes]
rs12280564	1.00[AMR][1000 genomes]
rs12283026	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12286152	1.00[AMR][1000 genomes]
rs13377317	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16929080	1.00[AMR][1000 genomes]
rs16929093	1.00[AMR][1000 genomes]
rs4150999	1.00[AMR][1000 genomes]
rs4151011	1.00[AMR][1000 genomes]
rs4151030	1.00[AMR][1000 genomes]
rs4151047	1.00[AMR][1000 genomes]
rs57273606	1.00[AMR][1000 genomes]
rs7119565	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9971624	0.95[AFR][1000 genomes];1.00[AMR][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	nsv467791	chr11:36108497-36999385	Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv554003	chr11:36108497-36999385	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv832123	chr11:36582872-36757443	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv467792	chr11:36624187-36898373	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv554005	chr11:36624187-36898373	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv467793	chr11:36632515-37171833	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv554006	chr11:36632515-37171833	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36707800-36713600	Weak transcription	Fetal Lung	lung
2	chr11:36708000-36715200	Enhancers	Dnd41	blood
3	chr11:36708800-36710600	Enhancers	Fetal Stomach	stomach
4	chr11:36710000-36711400	Flanking Active TSS	Fetal Thymus	thymus
5	chr11:36710200-36710400	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
6	chr11:36710200-36710800	Flanking Bivalent TSS/Enh	Thymus	Thymus

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