Variant report

Variant	rs146878511
Chromosome Location	chr8:63595581-63595582
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 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	nsv831340	chr8:63515126-63702660	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv890960	chr8:63516962-63629549	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv971594	chr8:63594002-63596416	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63572400-63602600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:63587400-63602600	Weak transcription	Fetal Brain Female	brain
3	chr8:63594600-63596400	Enhancers	Fetal Intestine Large	intestine
4	chr8:63594800-63596000	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr8:63594800-63596400	Enhancers	Fetal Intestine Small	intestine
6	chr8:63595000-63596400	Enhancers	Stomach Mucosa	stomach
7	chr8:63595400-63596400	Weak transcription	Left Ventricle	heart
8	chr8:63595400-63596400	Weak transcription	Right Atrium	heart
9	chr8:63595400-63596600	Enhancers	Duodenum Mucosa	Duodenum
10	chr8:63595400-63596600	Enhancers	Hela-S3	cervix

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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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