Variant report

Variant	rs115728692
Chromosome Location	chr4:97915446-97915447
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879640	chr4:97711707-98697586	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1005103	chr4:97914293-98011695	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97913400-97915800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr4:97913600-97916000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:97913600-97920800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr4:97913800-97916000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr4:97914400-97916000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:97914600-97915800	Enhancers	ES-UCSF4 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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