Variant report

Variant	rs143562313
Chromosome Location	chr6:64323772-64323773
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	nsv969415	chr6:64323751-64326310	Enhancers Weak transcription Active TSS	TF binding region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64322800-64323800	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr6:64323000-64324200	Enhancers	Primary hematopoietic stem cells	blood
3	chr6:64323000-64325400	Weak transcription	Pancreas	Pancrea
4	chr6:64323400-64324200	Weak transcription	K562	blood

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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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