Variant report

Variant	rs1525074
Chromosome Location	chr7:14756651-14756652
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:14756304..14757028-chr7:15055834..15056611,2	MCF-7	breast:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10228891	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10259838	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10262035	0.82[EUR][1000 genomes]
rs10278975	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10499462	0.89[ASN][1000 genomes]
rs12533352	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12536592	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12537147	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12539208	0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12669997	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12699654	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12699655	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12699658	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13231864	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13237347	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1357856	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1357871	0.82[EUR][1000 genomes]
rs1357872	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1404614	0.82[EUR][1000 genomes]
rs1525099	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1568846	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1568847	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17606181	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17668635	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17668761	0.95[ASN][1000 genomes]
rs1997040	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2293339	0.83[EUR][1000 genomes]
rs34587189	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35046572	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35731392	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4719417	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6461121	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6944222	0.81[ASN][1000 genomes]
rs6947566	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6954517	0.91[ASN][1000 genomes]
rs6965637	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6966274	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6974971	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71538884	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7784799	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7785767	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7791900	0.81[EUR][1000 genomes]
rs9639210	0.83[EUR][1000 genomes]
rs9639212	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9639213	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9784967	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1031041	chr7:14624127-14999201	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv538741	chr7:14624127-14999201	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv887712	chr7:14717872-14829858	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14712800-14775200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr7:14754200-14757600	Enhancers	Liver	Liver
3	chr7:14755000-14757000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr7:14755000-14757800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:14755600-14757000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr7:14756000-14756800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr7:14756000-14756800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:14756400-14757000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
9	chr7:14756600-14758000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr7:14756600-14758200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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