Variant report

Variant	rs558336363
Chromosome Location	chr4:98187219-98187220
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879640	chr4:97711707-98697586	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv822656	chr4:98172266-98187338	Enhancers	lncRNA	n/a	inside rSNPs	diseases
3	esv3467260	chr4:98172364-98187503	Enhancers	lncRNA	n/a	inside rSNPs	diseases
4	esv3467259	chr4:98172417-98187482	Enhancers	lncRNA	n/a	inside rSNPs	diseases
5	esv3467261	chr4:98172417-98187482	Enhancers	lncRNA	n/a	inside rSNPs	diseases
6	nsv822658	chr4:98172476-98187338	Enhancers	lncRNA	n/a	inside rSNPs	diseases
7	nsv822659	chr4:98172603-98187338	Enhancers	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98187200-98188200	Enhancers	Dnd41	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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