Variant report

Variant	rs188103581
Chromosome Location	chr4:125671652-125671653
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879882	chr4:125662969-125703938	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv3448689	chr4:125671052-125673050	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv8426	chr4:125671605-125672216	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3526159	chr4:125671616-125672175	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv3466178	chr4:125671618-125672157	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3526160	chr4:125671645-125672145	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:125668000-125672000	Weak transcription	Aorta	Aorta

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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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