Variant report

Variant	rs569785943
Chromosome Location	chr4:47050922-47050923
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	esv3389769	chr4:47050870-47051190	Weak transcription Enhancers	n/a	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	chr4:47050200-47052800	Enhancers	Brain Anterior Caudate	brain
2	chr4:47050400-47051000	Enhancers	Brain Cingulate Gyrus	brain
3	chr4:47050400-47051600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:47050400-47051600	Enhancers	Brain Substantia Nigra	brain
5	chr4:47050800-47051000	Enhancers	HUES64 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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