Variant report

Variant	rs72637963
Chromosome Location	chr1:47274891-47274892
allele	A/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	MYC	chr1:47274836-47275012	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:47266762..47268483-chr1:47274674..47276282,2	MCF-7	breast:

Variant related genes	Relation type
CYP4B1	TF binding region

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs11211366	0.84[ASN][1000 genomes]
rs11211369	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11211386	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11211387	0.86[EUR][1000 genomes]
rs1122582	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11576162	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11583378	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11584320	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11586184	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12402717	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12410657	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12566735	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12569216	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1572603	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1890246	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1890248	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1890249	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1890250	0.94[ASN][1000 genomes]
rs1890251	0.94[ASN][1000 genomes]
rs2185032	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2405335	0.81[ASN][1000 genomes]
rs3766195	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3766196	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3766197	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3820080	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3863632	0.81[EUR][1000 genomes]
rs4417002	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs45563134	0.84[ASN][1000 genomes]
rs4560983	0.84[EUR][1000 genomes]
rs4646482	0.81[ASN][1000 genomes]
rs4646486	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4646487	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4646492	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4646493	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4646495	0.86[ASN][1000 genomes]
rs4660960	0.96[EUR][1000 genomes]
rs55868139	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55936777	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs60430993	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61741519	0.81[EUR][1000 genomes]
rs67678353	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72681939	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs751027	0.82[ASN][1000 genomes]
rs7553652	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs837395	0.82[ASN][1000 genomes]
rs9728536	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001455	chr1:46828004-47326539	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv534950	chr1:46828004-47326539	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1013048	chr1:47132831-47377364	Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv534955	chr1:47132831-47377364	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1011086	chr1:47259078-47305191	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv870538	chr1:47259138-47309265	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1010063	chr1:47264205-47285118	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1004143	chr1:47270942-47321982	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47265600-47279200	Weak transcription	Gastric	stomach
2	chr1:47272400-47275600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:47273000-47275200	Weak transcription	Esophagus	oesophagus
4	chr1:47273400-47285600	Weak transcription	Spleen	Spleen
5	chr1:47273600-47275600	Weak transcription	Left Ventricle	heart
6	chr1:47273600-47275600	Weak transcription	Right Ventricle	heart
7	chr1:47273600-47276200	Weak transcription	Lung	lung
8	chr1:47273600-47276400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr1:47273600-47276400	Weak transcription	Right Atrium	heart
10	chr1:47273600-47276400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr1:47273800-47275200	Weak transcription	Placenta	Placenta
12	chr1:47273800-47275200	Weak transcription	Psoas Muscle	Psoas
13	chr1:47273800-47276000	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr1:47274000-47276000	Weak transcription	Adipose Nuclei	Adipose

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