Variant report

Variant	rs398001801
Chromosome Location	chr6:64324451-64324452
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 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
2	esv1239349	chr6:64324450-64324451	Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64323000-64325400	Weak transcription	Pancreas	Pancrea
2	chr6:64324400-64326000	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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