Variant report

Variant	rs13010697
Chromosome Location	chr2:141470480-141470481
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	chr2:141469791..141471888-chr2:141475142..141477938,2	MCF-7	breast:
2	chr2:141462311..141465013-chr2:141470003..141471554,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10180315	1.00[CEU][hapmap];0.88[JPT][hapmap]
rs10199928	1.00[CEU][hapmap];0.90[JPT][hapmap]
rs10207124	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs10209458	1.00[CEU][hapmap];0.90[JPT][hapmap]
rs11888646	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs11890215	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs11900908	0.93[CEU][hapmap];0.90[JPT][hapmap]
rs11900955	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11901574	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11902768	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12691557	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13383867	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs13385409	1.00[CEU][hapmap];0.90[JPT][hapmap]
rs13407299	1.00[CEU][hapmap];0.90[JPT][hapmap]
rs13411355	1.00[CEU][hapmap];0.89[JPT][hapmap]
rs13422197	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13431727	1.00[CEU][hapmap];0.89[JPT][hapmap]
rs1372253	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1441450	0.86[CEU][hapmap];0.90[JPT][hapmap]
rs1441457	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16844555	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17513652	1.00[CEU][hapmap];0.90[JPT][hapmap]
rs2380914	1.00[CEU][hapmap];0.90[JPT][hapmap]
rs34492262	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34914136	0.97[EUR][1000 genomes]
rs436323	1.00[CEU][hapmap];0.90[JPT][hapmap]
rs448816	1.00[CEU][hapmap];0.90[JPT][hapmap]
rs6749187	1.00[CEU][hapmap];0.89[JPT][hapmap]
rs72907443	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7570942	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875194	chr2:141391918-141504719	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv875195	chr2:141407101-141542081	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv583194	chr2:141409166-141471725	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv875196	chr2:141409166-141471725	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv875197	chr2:141409166-141478468	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv875198	chr2:141409166-141571329	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv875199	chr2:141409166-141600366	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv583196	chr2:141426714-141487897	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
9	nsv459540	chr2:141428751-141487897	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
10	nsv459552	chr2:141428751-141487897	Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
11	nsv583197	chr2:141428751-141487897	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
12	nsv875200	chr2:141448312-141504719	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
13	nsv875201	chr2:141448312-141561255	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv875202	chr2:141448312-141587228	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv875203	chr2:141448312-141592252	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141470000-141470600	Active TSS	Skeletal Muscle Female	skeletal muscle

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