Variant report

Variant	rs8007094
Chromosome Location	chr14:42486266-42486267
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 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
6	esv3528669	chr14:42486229-42486742	Weak transcription	n/a	n/a	inside rSNPs	n/a
7	esv3528675	chr14:42486234-42486729	Weak transcription	n/a	n/a	inside rSNPs	n/a
8	esv3528985	chr14:42486237-42486714	Weak transcription	n/a	n/a	inside rSNPs	n/a
9	esv3528672	chr14:42486247-42486691	Weak transcription	n/a	n/a	inside rSNPs	n/a
10	esv3528670	chr14:42486249-42486669	Weak transcription	n/a	n/a	inside rSNPs	n/a
11	esv3528940	chr14:42486257-42486704	Weak transcription	n/a	n/a	inside rSNPs	n/a
12	esv3528952	chr14:42486264-42486701	Weak transcription	n/a	n/a	inside rSNPs	n/a
13	esv3528671	chr14:42486267-42486690	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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