Variant report

Variant	rs536747102
Chromosome Location	chr6:23466821-23466822
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3499590	chr6:23459223-23467221	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	esv3502044	chr6:23459623-23467421	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv3502045	chr6:23459623-23467421	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv981369	chr6:23465968-23469623	Enhancers	n/a	n/a	inside rSNPs	n/a
5	esv2422291	chr6:23466080-23600459	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv601124	chr6:23466670-23506490	Enhancers Weak transcription	Chromatin interactive region	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	chr6:23466400-23467800	Enhancers	Fetal Brain Male	brain

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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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