Variant report

Variant	rs369079439
Chromosome Location	chr3:143838022-143838023
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877568	chr3:143621140-143992630	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv3365190	chr3:143642195-143925886	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1010117	chr3:143750590-144093775	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv536748	chr3:143750590-144093775	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1010213	chr3:143775358-143863149	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv591923	chr3:143776096-143862350	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv591924	chr3:143776096-143864780	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1008414	chr3:143779087-143853396	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv1009018	chr3:143797683-143868350	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv532633	chr3:143802417-144440646	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv591925	chr3:143821997-144019763	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv1007963	chr3:143836773-144000203	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv536750	chr3:143836773-144000203	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143825200-143842000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:143830000-143847200	Weak transcription	Aorta	Aorta
3	chr3:143831600-143838200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr3:143831600-143838600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr3:143832800-143838200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr3:143832800-143838200	Weak transcription	Fetal Brain Male	brain
7	chr3:143834200-143838200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr3:143834200-143838200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr3:143834200-143838400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr3:143834400-143838200	Weak transcription	Brain Angular Gyrus	brain
11	chr3:143834400-143838400	Weak transcription	Brain Substantia Nigra	brain
12	chr3:143836800-143839600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:143836800-143839800	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr3:143837200-143839000	Enhancers	Liver	Liver
15	chr3:143837200-143839000	Enhancers	Fetal Intestine Small	intestine
16	chr3:143837400-143838200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr3:143837400-143838400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr3:143837600-143839200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr3:143837800-143839200	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr3:143837800-143839200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr3:143838000-143839000	Enhancers	Fetal Intestine Large	intestine

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