Variant report

Variant	rs564598761
Chromosome Location	chr21:17364370-17364371
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 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
3	esv3338941	chr21:17363731-17364979	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 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	chr21:17363800-17364800	Weak transcription	Hela-S3	cervix

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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