Variant report

Variant	rs369859589
Chromosome Location	chr5:68118303-68118304
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	esv3434869	chr5:68117677-68121030	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68115200-68118600	Weak transcription	Brain Angular Gyrus	brain
2	chr5:68117400-68118600	Weak transcription	Brain Hippocampus Middle	brain
3	chr5:68117400-68118600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr5:68117400-68118600	Weak transcription	Brain Substantia Nigra	brain
5	chr5:68118200-68118800	Enhancers	Fetal Kidney	kidney
6	chr5:68118200-68119200	Enhancers	HepG2	liver
7	chr5:68118200-68120200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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