Variant report

Variant	rs3733455
Chromosome Location	chr4:91648634-91648635
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:91643291..91645856-chr4:91647962..91650916,2	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11097265	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17017577	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2123954	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2271591	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3733453	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62309559	1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs62312977	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62312980	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62312983	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62312984	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62312985	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62312986	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62312987	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62312992	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62312994	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62312997	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62313022	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62313025	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62313055	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs62313056	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62313057	0.93[ASN][1000 genomes]
rs62313058	0.81[AMR][1000 genomes]
rs62314424	0.93[ASN][1000 genomes]
rs62314427	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62314446	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6841566	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs720327	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs72663610	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs72663613	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7681018	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931074	chr4:90970476-91753697	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv534470	chr4:91342219-91842807	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv879547	chr4:91546380-91661217	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv879548	chr4:91558486-91661217	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv4420	chr4:91616307-91661796	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv428766	chr4:91618397-91768647	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91644200-91649200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:91648400-91648800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:91648400-91649200	Weak transcription	Gastric	stomach
4	chr4:91648400-91650000	Enhancers	NHEK	skin
5	chr4:91648400-91650400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr4:91648600-91648800	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr4:91648600-91649000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr4:91648600-91649000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:91648600-91649400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:91648600-91649800	Enhancers	H9 Cell Line	embryonic stem cell
11	chr4:91648600-91649800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:91648600-91650000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:91648600-91650000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:91648600-91650000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:91648600-91650000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:91648600-91650200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:91648600-91650200	Enhancers	HMEC	breast
18	chr4:91648600-91650400	Enhancers	HUES64 Cell Line	embryonic stem cell

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