Variant report

Variant	rs71602763
Chromosome Location	chr5:1885111-1885112
allele	-/G
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	CTBP2	chr5:1882832-1885692	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr5:1882409-1891588	MCF10A-Er-Src	breast:	n/a	n/a
3	ZNF143	chr5:1884757-1885262	H1-hESC	embryonic stem cell:	n/a	n/a
4	STAT3	chr5:1885079-1885337	MCF10A-Er-Src	breast:	n/a	n/a
5	POLR2A	chr5:1881481-1891348	MCF10A-Er-Src	breast:	n/a	n/a
6	SUZ12	chr5:1885091-1887033	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:1793765..1806799-chr5:1879445..1889322,45	MCF-7	breast:
2	chr5:1796457..1805482-chr5:1878036..1885786,21	MCF-7	breast:
3	chr5:1881475..1885354-chr5:1933918..1938503,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000249326	TF binding region
IRX4	TF binding region
ENSG00000248994	Chromatin interaction
ENSG00000145494	Chromatin interaction
ENSG00000171421	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 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	nsv881619	chr5:1822326-1886471	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv881557	chr5:1822326-1932463	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv596892	chr5:1832240-1892759	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	nsv596893	chr5:1839498-1892759	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv881470	chr5:1850563-1892759	Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv881188	chr5:1852284-1892759	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv822962	chr5:1877770-1888630	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	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
12	nsv822963	chr5:1884480-1885198	Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:1879800-1885200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr5:1880800-1887800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
3	chr5:1881200-1885200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
4	chr5:1881400-1886800	Bivalent Enhancer	Fetal Stomach	stomach
5	chr5:1881600-1885600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
6	chr5:1882400-1885400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
7	chr5:1882400-1887600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:1882400-1887600	Active TSS	NHEK	skin
9	chr5:1882400-1887800	Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr5:1883000-1885200	Active TSS	HMEC	breast
11	chr5:1883600-1886800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr5:1883800-1885400	Bivalent Enhancer	Brain Hippocampus Middle	brain
13	chr5:1884200-1885400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr5:1884200-1885400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
15	chr5:1884200-1885600	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr5:1884200-1898200	Weak transcription	Gastric	stomach
17	chr5:1884400-1885200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:1884400-1886000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr5:1884400-1886400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:1884400-1887000	Weak transcription	Right Atrium	heart
21	chr5:1884800-1885200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr5:1884800-1885200	Flanking Active TSS	Fetal Heart	heart
23	chr5:1884800-1885400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
24	chr5:1884800-1885400	Bivalent Enhancer	Lung	lung
25	chr5:1884800-1885600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
26	chr5:1884800-1886400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
27	chr5:1885000-1885200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
28	chr5:1885000-1885200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
29	chr5:1885000-1885400	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:1885000-1885400	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:1885000-1885400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
32	chr5:1885000-1885400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr5:1885000-1885400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:1885000-1885400	Enhancers	Right Ventricle	heart
35	chr5:1885000-1885600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr5:1885000-1886600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr5:1885000-1887800	Active TSS	Esophagus	oesophagus

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