Variant report

Variant	rs376739662
Chromosome Location	chr4:118723383-118723384
allele	A/T
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	nsv879838	chr4:118681261-118753062	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv10555	chr4:118723143-118725551	Enhancers Weak transcription	Chromatin interactive region	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	chr4:118720200-118723400	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr4:118720800-118726000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr4:118722600-118723800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:118722800-118723800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr4:118723200-118728000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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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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