Variant report

Variant	rs538366508
Chromosome Location	chr5:116489719-116489720
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752839	chr5:116461101-116504101	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
2	esv3335438	chr5:116488253-116491451	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
3	esv3333294	chr5:116488903-116491301	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
4	esv1698181	chr5:116489718-116489719	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116485600-116497600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:116489000-116494200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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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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