Variant report

Variant	rs371965023
Chromosome Location	chr6:55492760-55492761
allele	-/AT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1026411	chr6:55372845-55653498	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv3474008	chr6:55491689-55494295	Weak transcription	n/a	n/a	inside rSNPs	diseases
4	esv3474009	chr6:55491689-55494295	Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3393454	chr6:55491818-55494366	Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3429791	chr6:55491968-55494116	Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3448204	chr6:55492428-55493097	Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3508049	chr6:55492439-55493150	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3508048	chr6:55492556-55493057	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3508050	chr6:55492677-55493003	Weak transcription	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	chr6:55479400-55504000	Weak transcription	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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