Variant report

Variant	rs577242910
Chromosome Location	chr9:85846514-85846515
allele	C/T
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	esv3411346	chr9:85846079-85846997	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85844200-85850600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr9:85845400-85846800	Enhancers	Fetal Heart	heart
3	chr9:85845400-85846800	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr9:85845600-85846800	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr9:85845800-85846600	Enhancers	Fetal Muscle Leg	muscle
6	chr9:85846000-85846600	Enhancers	Placenta	Placenta
7	chr9:85846200-85846600	Enhancers	Left Ventricle	heart
8	chr9:85846200-85846600	Enhancers	Psoas Muscle	Psoas
9	chr9:85846400-85846600	Enhancers	Right Atrium	heart
10	chr9:85846400-85854000	Weak transcription	Pancreas	Pancrea

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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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