Variant report

Variant	rs532448810
Chromosome Location	chr8:36243386-36243387
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034989	chr8:36242017-36436244	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	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	chr8:36243000-36243400	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr8:36243000-36243600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:36243000-36243600	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr8:36243200-36243600	Enhancers	H9 Cell Line	embryonic stem cell
5	chr8:36243200-36243600	Enhancers	HUES48 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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