Variant report

Variant	rs13280676
Chromosome Location	chr8:63782773-63782774
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831341	chr8:63658694-63852213	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1033527	chr8:63673915-64073735	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv890962	chr8:63708519-63812686	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv3376189	chr8:63781948-63784421	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3439081	chr8:63782023-63784571	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3403225	chr8:63782398-63783946	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3481411	chr8:63782656-63783418	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3529892	chr8:63782684-63783411	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3529891	chr8:63782719-63783358	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3529893	chr8:63782719-63783358	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3345005	chr8:63782758-63783448	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	chr8:63782000-63792200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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