Variant report

Variant	rs201315616
Chromosome Location	chr9:85846164-85846165
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2365047	chr9:85845962-85846368	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3492346	chr9:85846046-85846214	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3492345	chr9:85846046-85846239	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3411346	chr9:85846079-85846997	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv3492347	chr9:85846105-85846228	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 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

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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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