Variant report

Variant	rs554022989
Chromosome Location	chr5:1933585-1933586
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr5:1933413-1934632	HCT-116	colon:	n/a	chr5:1934230-1934241 chr5:1934231-1934240 chr5:1934227-1934242 chr5:1934231-1934241 chr5:1934230-1934241 chr5:1934229-1934242
2	POLR2A	chr5:1927991-1933825	MCF10A-Er-Src	breast:	n/a	n/a
3	YY1	chr5:1933494-1933713	HCT-116	colon:	n/a	n/a
4	FOSL1	chr5:1933341-1934506	HCT-116	colon:	n/a	chr5:1933699-1933706 chr5:1934197-1934206 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
5	JUND	chr5:1933347-1934319	HCT-116	colon:	n/a	chr5:1933699-1933706 chr5:1934197-1934206 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
6	TCF7L2	chr5:1933342-1934596	HCT-116	colon:	n/a	chr5:1933698-1933707 chr5:1933710-1933726 chr5:1933711-1933725 chr5:1933710-1933726
7	FOS	chr5:1933352-1933871	MCF10A-Er-Src	breast:	n/a	chr5:1933699-1933706 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
8	JUND	chr5:1933359-1934441	HCT-116	colon:	n/a	chr5:1933699-1933706 chr5:1934197-1934206 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
9	FOSL1	chr5:1933406-1934456	HCT-116	colon:	n/a	chr5:1933699-1933706 chr5:1934197-1934206 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
10	FOS	chr5:1933517-1933860	MCF10A-Er-Src	breast:	n/a	chr5:1933699-1933706 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
11	MYC	chr5:1933526-1933767	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr5:1933519-1933861	MCF10A-Er-Src	breast:	n/a	chr5:1933699-1933706 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
13	SP1	chr5:1933358-1934603	HCT-116	colon:	n/a	chr5:1934178-1934192

Variant related genes	Relation type
ENSG00000248994	TF binding region

Extended variants
information (count: 19 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933805	chr5:1450724-1941619	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv817407	chr5:1495354-2191460	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
3	nsv869236	chr5:1719263-2259100	Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
4	nsv880886	chr5:1880891-1936443	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv880460	chr5:1886471-1936443	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv915846	chr5:1891098-2167677	Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv881650	chr5:1892995-1944487	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv880653	chr5:1892995-1946697	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1015576	chr5:1894124-1942909	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	nsv880562	chr5:1895829-1936443	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv881174	chr5:1895829-1942834	Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
12	nsv880381	chr5:1895829-1946697	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	nsv1026930	chr5:1898993-2126061	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
14	nsv508344	chr5:1905222-1976860	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv881562	chr5:1907974-1976187	Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv880964	chr5:1912921-1953161	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
17	nsv596897	chr5:1924628-1934490	Bivalent Enhancer Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
18	nsv980962	chr5:1932426-1945863	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
19	nsv516663	chr5:1932463-1934666	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr5:1932000-1943200	Weak transcription	Esophagus	oesophagus
2	chr5:1932000-1950800	Weak transcription	Gastric	stomach
3	chr5:1932200-1933800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:1932200-1934200	Weak transcription	Pancreas	Pancrea
5	chr5:1932200-1934400	Weak transcription	Brain Anterior Caudate	brain
6	chr5:1932200-1934400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr5:1932200-1934800	Weak transcription	Ovary	ovary
8	chr5:1932200-1935000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr5:1932200-1935000	Weak transcription	Left Ventricle	heart
10	chr5:1932200-1937600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr5:1932200-1937600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:1932200-1942200	Weak transcription	Stomach Smooth Muscle	stomach
13	chr5:1932200-1945600	Weak transcription	Right Ventricle	heart
14	chr5:1932200-1946400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:1932400-1936600	Weak transcription	Adipose Nuclei	Adipose
16	chr5:1933000-1933600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr5:1933000-1934000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr5:1933000-1938200	Enhancers	HMEC	breast
19	chr5:1933000-1942200	Weak transcription	Brain Cingulate Gyrus	brain
20	chr5:1933200-1933800	Enhancers	NHEK	skin
21	chr5:1933400-1933800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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