Variant report

Variant	rs368939916
Chromosome Location	chr14:42486199-42486200
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv564563	chr14:42477256-42644617	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2496148	chr14:42485616-42487254	Weak transcription	n/a	n/a	inside rSNPs	n/a
3	esv3442835	chr14:42485652-42487650	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
4	esv8031	chr14:42486110-42486827	Weak transcription	n/a	n/a	inside rSNPs	n/a
5	esv2011237	chr14:42486134-42486835	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42484200-42487400	Weak transcription	Primary B cells from cord blood	blood

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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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