Variant report

Variant	rs9920822
Chromosome Location	chr15:78661349-78661350
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs2037348	0.89[EUR][1000 genomes]

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	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv917303	chr15:78491050-79205255	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
3	nsv833063	chr15:78605215-78754945	Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv1052910	chr15:78608637-78707049	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78651600-78666600	Weak transcription	Pancreas	Pancrea
2	chr15:78653600-78662400	Weak transcription	Right Ventricle	heart
3	chr15:78658800-78665200	Weak transcription	Right Atrium	heart
4	chr15:78660200-78662400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr15:78660400-78661600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:78660400-78661800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr15:78660400-78662800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:78660400-78662800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr15:78660600-78662000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr15:78660800-78661400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr15:78660800-78661400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr15:78661000-78661400	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr15:78661200-78662000	Weak transcription	Duodenum Mucosa	Duodenum
14	chr15:78661200-78663000	Enhancers	Stomach Mucosa	stomach
15	chr15:78661200-78664200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr15:78661200-78664600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr15:78661200-78667200	Weak transcription	HUES6 Cell Line	embryonic stem cell

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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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