Variant report

Variant	rs59164803
Chromosome Location	chr3:50526353-50526354
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	chr3:50524606..50527623-chr3:50538971..50541993,3	K562	blood:
2	chr3:50525621..50528608-chr3:50539997..50541654,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000007402	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs17050967	1.00[AMR][1000 genomes]
rs17050976	1.00[AMR][1000 genomes]
rs17050977	1.00[AMR][1000 genomes]
rs57278600	1.00[AMR][1000 genomes]
rs58124375	0.83[AFR][1000 genomes]
rs59896933	0.81[AFR][1000 genomes]
rs61601450	1.00[AMR][1000 genomes]
rs61638172	0.81[AFR][1000 genomes]
rs72934837	1.00[AMR][1000 genomes]
rs72936957	1.00[AMR][1000 genomes]
rs72936959	1.00[AMR][1000 genomes]
rs72936962	1.00[AMR][1000 genomes]
rs72936972	1.00[AMR][1000 genomes]
rs72936980	1.00[AMR][1000 genomes]
rs72936982	1.00[AMR][1000 genomes]
rs72937000	1.00[AMR][1000 genomes]
rs72938708	1.00[AMR][1000 genomes]
rs72938719	1.00[AMR][1000 genomes]
rs72938734	0.81[AFR][1000 genomes]
rs72938738	0.82[AFR][1000 genomes]
rs72938740	0.82[AFR][1000 genomes]
rs72938750	0.81[AFR][1000 genomes]

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	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
3	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
4	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
5	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
6	esv3584502	chr3:50368278-50659741	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
7	nsv432419	chr3:50388396-50637496	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
8	nsv1013225	chr3:50440826-50700448	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv536566	chr3:50440826-50700448	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
10	nsv984540	chr3:50473691-50669310	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
11	nsv1012501	chr3:50483037-50679591	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
12	nsv536567	chr3:50483037-50679591	Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	esv998611	chr3:50519293-50526732	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50492600-50528400	Weak transcription	Gastric	stomach
2	chr3:50513000-50527400	Weak transcription	Right Atrium	heart
3	chr3:50520200-50527800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:50520400-50530400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr3:50520800-50528400	Weak transcription	Spleen	Spleen
6	chr3:50522000-50533600	Weak transcription	Lung	lung
7	chr3:50522800-50528000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr3:50523800-50527200	Weak transcription	Fetal Muscle Leg	muscle
9	chr3:50525000-50528200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr3:50525400-50527200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:50525400-50528000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr3:50525400-50528000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr3:50525600-50527400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:50525600-50527800	Weak transcription	Fetal Thymus	thymus
15	chr3:50525600-50528000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr3:50525800-50528000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr3:50525800-50528000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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