Variant report

Variant	rs533839019
Chromosome Location	chr18:24473802-24473803
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761995	chr18:24214286-24502570	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv961040	chr18:24470692-24474008	Weak transcription Enhancers Active TSS	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24473800-24474000	Enhancers	H9 Cell Line	embryonic stem cell
2	chr18:24473800-24474200	Active TSS	Skeletal Muscle Female	skeletal muscle
3	chr18:24473800-24474600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr18:24473800-24474800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr18:24473800-24475400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr18:24473800-24475600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr18:24473800-24475600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr18:24473800-24476000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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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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