Variant report

Variant	rs200075798
Chromosome Location	chr10:23433952-23433953
allele	G/T
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	esv3427167	chr10:23433696-23435794	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	inside rSNPs	diseases
2	esv2276149	chr10:23433950-23433956	Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv1386687	chr10:23433950-23433956	Weak transcription	n/a	n/a	inside rSNPs	diseases
4	esv2493475	chr10:23433951-23433956	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23433000-23437200	Weak transcription	Pancreas	Pancrea
2	chr10:23433600-23434600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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