Variant report

Variant	rs537956425
Chromosome Location	chr6:82567272-82567273
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830712	chr6:82491029-82654531	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3353008	chr6:82567151-82567322	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv3398957	chr6:82567171-82567292	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82555600-82567400	Weak transcription	Aorta	Aorta
2	chr6:82558200-82572000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr6:82565600-82569400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:82565600-82569600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr6:82565600-82572200	Weak transcription	HepG2	liver
6	chr6:82566400-82568200	Enhancers	Stomach Mucosa	stomach

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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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