Variant report

Variant	rs114080373
Chromosome Location	chr7:96550175-96550176
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	nsv607874	chr7:96543340-96550696	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96549800-96551200	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr7:96549800-96551200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr7:96550000-96550200	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr7:96550000-96551000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr7:96550000-96551200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr7:96550000-96551400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr7:96550000-96551400	Enhancers	NHEK	skin
8	chr7:96550000-96551600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	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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