Variant report

Variant	rs74017465
Chromosome Location	chr15:53869239-53869240
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10518730	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12437669	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12439465	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12439520	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12439540	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12439608	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12439700	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12441277	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12442549	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966231	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966232	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966247	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966254	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966257	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966258	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966261	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966270	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966272	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966273	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966274	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966276	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966278	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966280	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966282	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966284	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966301	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966302	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966304	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966308	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17662369	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs17662393	0.93[AMR][1000 genomes]
rs1906396	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1906398	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1906399	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1906442	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2414244	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2414247	1.00[ASN][1000 genomes]
rs35968624	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4457943	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4468551	1.00[ASN][1000 genomes]
rs55799724	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55933865	0.87[AMR][1000 genomes]
rs56007818	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56276502	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56771214	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57388125	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs58124844	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59074347	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59125438	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59287715	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59627084	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60027343	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60909239	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61301076	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61355899	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61554251	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7164313	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7165282	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7165440	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7170810	1.00[ASN][1000 genomes]
rs7171176	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7171226	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7171619	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7171820	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7171915	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7172085	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7172090	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7172762	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7173966	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408216	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408217	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408222	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408230	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408236	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408239	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74015825	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74017460	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs74017462	0.85[AMR][1000 genomes]
rs74017470	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74018056	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74018057	0.85[EUR][1000 genomes]
rs8037868	1.00[ASN][1000 genomes]
rs8038018	1.00[ASN][1000 genomes]
rs8039231	1.00[ASN][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	nsv904223	chr15:53665247-54340070	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv904224	chr15:53668018-54210677	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1052235	chr15:53677524-54618723	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv542388	chr15:53677524-54618723	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv833009	chr15:53752901-53935303	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv9267	chr15:53821005-54132612	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv904225	chr15:53840665-53878948	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
8	nsv569435	chr15:53845097-53966805	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53862200-53872400	Weak transcription	Liver	Liver
2	chr15:53865400-53872600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:53865800-53869600	Weak transcription	NHEK	skin
4	chr15:53868400-53869600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr15:53868400-53869800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr15:53868800-53869400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr15:53868800-53869800	Enhancers	Brain Hippocampus Middle	brain
8	chr15:53869000-53869400	Flanking Active TSS	Brain Substantia Nigra	brain
9	chr15:53869000-53869600	Enhancers	HMEC	breast

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