Variant report

Variant	rs62005912
Chromosome Location	chr15:53850892-53850893
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:53839749..53842575-chr15:53848742..53851441,2	MCF-7	breast:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10444799	0.89[ASN][1000 genomes]
rs10444830	0.89[ASN][1000 genomes]
rs10518727	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11070988	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11070989	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11070990	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12438390	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12440270	0.82[ASN][1000 genomes]
rs12440842	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12442849	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12442851	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966177	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16966184	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966209	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16966210	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17548678	0.89[ASN][1000 genomes]
rs17630504	0.89[ASN][1000 genomes]
rs17630697	0.89[ASN][1000 genomes]
rs1906424	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1906425	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1906426	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2129774	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2220382	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2220383	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2414242	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28760919	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3088091	0.89[ASN][1000 genomes]
rs3206108	0.89[ASN][1000 genomes]
rs56916135	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57855113	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs609401	0.89[ASN][1000 genomes]
rs62005869	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62005872	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62005873	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62005874	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62005881	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62005902	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62005903	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62005905	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62005906	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62005908	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62005909	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62005911	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62007573	0.89[ASN][1000 genomes]
rs6493631	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7161989	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7162024	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7178004	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73406225	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74017420	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8030213	0.89[ASN][1000 genomes]
rs953521	0.89[ASN][1000 genomes]

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	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	nsv1040216	chr15:53743780-53851679	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	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
7	nsv1038512	chr15:53803770-53851679	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	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
9	nsv569433	chr15:53828686-53860607	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	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
11	nsv569434	chr15:53845097-53860607	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
12	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:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53842400-53851000	Weak transcription	Liver	Liver
2	chr15:53842600-53851000	Weak transcription	Fetal Intestine Small	intestine
3	chr15:53843600-53852200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr15:53844200-53852200	Weak transcription	Small Intestine	intestine
5	chr15:53847800-53851800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr15:53848000-53851000	Weak transcription	Primary hematopoietic stem cells	blood
7	chr15:53848800-53851000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr15:53849000-53851200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr15:53850600-53851800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr15:53850600-53851800	Enhancers	HepG2	liver
11	chr15:53850600-53852600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr15:53850600-53853200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr15:53850600-53853800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr15:53850800-53851600	Weak transcription	Brain Germinal Matrix	brain
15	chr15:53850800-53851800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr15:53850800-53852200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr15:53850800-53852800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr15:53850800-53853600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr15:53850800-53854000	Enhancers	Fetal Intestine Large	intestine
20	chr15:53850800-53854800	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links