Variant report

Variant	rs570265400
Chromosome Location	chr8:121094597-121094598
allele	-/AACA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	esv3348294	chr8:121000288-121250984	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1025923	chr8:121093383-121108706	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121075600-121095800	Weak transcription	Gastric	stomach
2	chr8:121091000-121094600	Weak transcription	Ovary	ovary
3	chr8:121091200-121095400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr8:121093000-121094600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr8:121093400-121095000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:121093400-121095000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:121093400-121095800	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr8:121094400-121094800	Enhancers	HepG2	liver
9	chr8:121094400-121095400	Enhancers	Fetal Intestine Large	intestine
10	chr8:121094400-121095800	Enhancers	NH-A	brain
11	chr8:121094400-121096000	Enhancers	Placenta	Placenta
12	chr8:121094400-121097400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr8:121094400-121097600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:121094400-121097600	Enhancers	Osteobl	bone
15	chr8:121094400-121098000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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