Variant report

Variant	rs193194296
Chromosome Location	chr3:79248624-79248625
allele	A/G
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	esv2763281	chr3:79246361-79489765	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:79248400-79250200	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr3:79248600-79249800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:79248600-79250000	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr3:79248600-79251800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr3:79248600-79251800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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