Variant report

Variant	rs560479528
Chromosome Location	chr16:59283065-59283066
allele	A/C
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	nsv833247	chr16:59132198-59293527	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv833249	chr16:59282950-59461023	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:59282200-59283200	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr16:59282400-59283200	Enhancers	H1 Cell Line	embryonic stem cell
3	chr16:59282400-59283200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr16:59282400-59283200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr16:59282400-59283200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr16:59282400-59283200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr16:59282400-59283400	Enhancers	Fetal Muscle Leg	muscle
8	chr16:59282600-59283200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr16:59282800-59283200	Enhancers	iPS-15b 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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