Variant report

Variant	rs184170998
Chromosome Location	chr4:98173965-98173966
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 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	esv2421442	chr4:98172414-98185132	Enhancers	lncRNA	n/a	inside rSNPs	diseases
5	nsv442913	chr4:98172414-98185132	Enhancers	lncRNA	n/a	inside rSNPs	diseases
6	esv3467259	chr4:98172417-98187482	Enhancers	lncRNA	n/a	inside rSNPs	diseases
7	esv3467261	chr4:98172417-98187482	Enhancers	lncRNA	n/a	inside rSNPs	diseases
8	nsv822657	chr4:98172476-98187201	Enhancers	lncRNA	n/a	inside rSNPs	diseases
9	nsv822658	chr4:98172476-98187338	Enhancers	lncRNA	n/a	inside rSNPs	diseases
10	nsv822659	chr4:98172603-98187338	Enhancers	lncRNA	n/a	inside rSNPs	diseases
11	nsv514234	chr4:98173937-98183545	Enhancers	n/a	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	chr4:98173800-98174000	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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