Variant report

Variant	rs371424036
Chromosome Location	chr4:96528477-96528478
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2648717	chr4:96527343-96529922	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv2404517	chr4:96528231-96529879	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3465762	chr4:96528284-96529799	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3465758	chr4:96528336-96529769	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3465759	chr4:96528341-96529760	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3465760	chr4:96528356-96529719	Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3465761	chr4:96528410-96529690	Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3465763	chr4:96528424-96529686	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96527800-96528600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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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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