Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:17364798..17365299-chr9:107784199..107784699,2	Hela-S3	cervix:

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs16990117	1.00[EUR][1000 genomes]
rs16990578	1.00[EUR][1000 genomes]
rs16990828	1.00[EUR][1000 genomes]
rs16992521	1.00[EUR][1000 genomes]
rs16992557	1.00[EUR][1000 genomes]
rs16992628	1.00[EUR][1000 genomes]
rs366082	1.00[EUR][1000 genomes]
rs367091	1.00[EUR][1000 genomes]
rs392028	1.00[EUR][1000 genomes]
rs41384050	1.00[EUR][1000 genomes]
rs56141957	1.00[EUR][1000 genomes]
rs58289432	1.00[EUR][1000 genomes]
rs58297914	1.00[EUR][1000 genomes]
rs59169113	1.00[EUR][1000 genomes]
rs73346759	1.00[EUR][1000 genomes]
rs73892584	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73892585	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73892591	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73892592	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73892593	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73892594	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73892599	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73892601	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73894705	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73894706	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73894707	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73894709	1.00[EUR][1000 genomes]
rs73894710	1.00[EUR][1000 genomes]
rs764003	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064664	chr21:17336936-17405756	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3376626	chr21:17363331-17365429	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17363400-17365200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr21:17363400-17365600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr21:17363400-17365600	Enhancers	HUVEC	blood vessel
4	chr21:17363600-17365200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr21:17364400-17365200	Enhancers	HSMM	muscle
6	chr21:17364600-17365200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr21:17364600-17365200	Enhancers	Osteobl	bone
8	chr21:17364800-17365200	Enhancers	Hela-S3	cervix
9	chr21:17364800-17365200	Enhancers	NH-A	brain
10	chr21:17364800-17368400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr21:17365000-17367400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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