Variant report

Variant	rs11802447
Chromosome Location	chr1:158361185-158361186
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10218454	0.96[AFR][1000 genomes]
rs10218671	1.00[EUR][1000 genomes]
rs10218835	0.84[AFR][1000 genomes]
rs11799342	0.92[EUR][1000 genomes]
rs11799345	0.92[EUR][1000 genomes]
rs11800438	1.00[EUR][1000 genomes]
rs11807406	0.92[EUR][1000 genomes]
rs11807851	0.92[EUR][1000 genomes]
rs11808256	0.92[EUR][1000 genomes]
rs11809338	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11810662	1.00[EUR][1000 genomes]
rs11810950	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11810954	0.85[EUR][1000 genomes]
rs11811766	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1321643	1.00[EUR][1000 genomes]
rs1321644	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13376124	1.00[EUR][1000 genomes]
rs16840119	1.00[EUR][1000 genomes]
rs57394063	0.92[EUR][1000 genomes]
rs57853663	0.92[EUR][1000 genomes]
rs58034709	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58407932	1.00[EUR][1000 genomes]
rs58929010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59924999	0.92[EUR][1000 genomes]
rs60368784	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61275000	0.92[EUR][1000 genomes]
rs61469898	1.00[EUR][1000 genomes]
rs6701913	1.00[EUR][1000 genomes]
rs73012040	0.92[EUR][1000 genomes]
rs73012047	0.92[EUR][1000 genomes]
rs73012048	0.92[EUR][1000 genomes]
rs73012049	0.92[EUR][1000 genomes]
rs73012050	0.92[EUR][1000 genomes]
rs73012051	0.92[EUR][1000 genomes]
rs73013909	0.92[EUR][1000 genomes]
rs73013913	0.92[EUR][1000 genomes]
rs73013914	0.92[EUR][1000 genomes]
rs73013916	0.92[EUR][1000 genomes]
rs73013917	0.92[EUR][1000 genomes]
rs73013920	0.92[EUR][1000 genomes]
rs73013941	1.00[EUR][1000 genomes]
rs73013974	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73015892	1.00[EUR][1000 genomes]
rs74121316	0.92[EUR][1000 genomes]
rs74121366	1.00[EUR][1000 genomes]
rs7537699	1.00[AMR][1000 genomes];1.00[EUR][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	nsv999542	chr1:158015715-158368132	Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv872479	chr1:158118787-158484285	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv872480	chr1:158153526-158450238	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv831692	chr1:158223459-158392016	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv998569	chr1:158317392-158443389	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island lncRNA	6 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	chr1:158358800-158362600	Enhancers	Dnd41	blood
2	chr1:158359800-158361200	Enhancers	Thymus	Thymus
3	chr1:158360200-158363800	Weak transcription	Primary B cells from cord blood	blood
4	chr1:158360400-158362000	Enhancers	Fetal Thymus	thymus
5	chr1:158360800-158364000	Weak transcription	Primary T cells from cord blood	blood

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