Variant report

Variant	rs184821593
Chromosome Location	chr4:30683382-30683383
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3464996	chr4:30683180-30683471	Enhancers	n/a	n/a	inside rSNPs	diseases
2	esv3805	chr4:30683205-30683506	Enhancers	n/a	n/a	inside rSNPs	diseases
3	esv3464995	chr4:30683233-30683440	Enhancers	n/a	n/a	inside rSNPs	diseases
4	esv3464998	chr4:30683247-30683436	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30683200-30684000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

Quick Search:

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

what's new

Quick links