Variant report

Variant	rs576805846
Chromosome Location	chr8:35419038-35419039
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 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	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
4	nsv1024397	chr8:35296922-35424277	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv533420	chr8:35358115-36227536	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	esv1799001	chr8:35414987-35422131	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3399250	chr8:35418810-35422308	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv2444089	chr8:35419038-35419038	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv2044164	chr8:35419038-35419039	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35414800-35424200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:35415000-35423400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr8:35415000-35431000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr8:35416000-35419200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:35417800-35419200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr8:35418800-35423000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr8:35418800-35423200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr8:35419000-35421600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:35419000-35423200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr8:35419000-35423400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr8:35419000-35430200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr8:35419000-35439400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:35419000-35439600	Weak transcription	H1 Cell Line	embryonic stem cell

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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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