Variant report

Variant	rs3784057
Chromosome Location	chr14:72449287-72449288
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	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72442800-72450200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr14:72442800-72450200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr14:72446000-72457000	Weak transcription	Right Ventricle	heart
4	chr14:72449000-72449400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
5	chr14:72449200-72449400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr14:72449200-72449400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr14:72449200-72449600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr14:72449200-72449600	Enhancers	ES-UCSF4 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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