Variant report

Variant	rs532148898
Chromosome Location	chr8:35196335-35196336
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017085	chr8:34742896-35594241	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv539546	chr8:34742896-35594241	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv429910	chr8:35021411-35257445	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv520421	chr8:35155517-35479468	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv890717	chr8:35184361-35315188	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv14971	chr8:35195413-35201496	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35185400-35204000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:35187800-35200200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr8:35188800-35201000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr8:35188800-35201000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr8:35189800-35200200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr8:35190600-35201400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr8:35191600-35199800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr8:35193800-35196800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr8:35195000-35196600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:35195800-35196600	Enhancers	Fetal Brain Male	brain
11	chr8:35196000-35196400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr8:35196000-35196400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr8:35196000-35198400	Enhancers	Fetal Heart	heart
14	chr8:35196200-35196400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:35196200-35196800	Enhancers	Brain Angular Gyrus	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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