Variant report

Variant	rs533978579
Chromosome Location	chr4:46983141-46983142
allele	C/T
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	nsv470031	chr4:46982218-47006399	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:46978400-46986400	Weak transcription	Fetal Brain Male	brain
2	chr4:46978600-46983800	Weak transcription	Brain Anterior Caudate	brain
3	chr4:46982200-46983200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:46982200-46983200	Enhancers	NHEK	skin
5	chr4:46982800-46983200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:46983000-46983800	Enhancers	Fetal Brain Female	brain
7	chr4:46983000-46984200	Enhancers	hESC Derived CD184+ Endoderm 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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