Variant report

Variant	rs6972609
Chromosome Location	chr7:52737635-52737636
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11238219	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11768808	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs11972154	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11978199	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11979296	0.88[ASN][1000 genomes]
rs12536581	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12539018	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12671544	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12671546	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12718695	0.80[ASN][1000 genomes]
rs13239908	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1470215	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17135230	0.80[ASN][1000 genomes]
rs34047048	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34063331	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34567158	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35117099	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35943655	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36162165	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62444475	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6955260	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6959309	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6961488	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6971491	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6972285	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6972623	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6973136	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6973629	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7810220	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9690639	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9691401	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888026	chr7:52588348-53013671	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv888027	chr7:52588348-53190508	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1019211	chr7:52706930-52785302	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1023637	chr7:52714035-52742733	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv606989	chr7:52722432-52748535	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv606990	chr7:52724902-52750565	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv606991	chr7:52727932-52743776	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv517177	chr7:52728891-52743776	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv818502	chr7:52728891-52743776	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv17724	chr7:52730103-52745307	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv2421635	chr7:52733291-52743776	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv464446	chr7:52733291-52748535	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv464447	chr7:52733291-52748535	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv606992	chr7:52733291-52748535	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv606993	chr7:52733291-52750565	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv818503	chr7:52733528-52743776	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv526376	chr7:52733528-52748535	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv464448	chr7:52733528-52752234	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv606994	chr7:52733528-52752234	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv606995	chr7:52733528-52757076	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv981771	chr7:52735792-52762504	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv442045	chr7:52736723-52742396	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
23	esv2764055	chr7:52736727-52749772	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv514420	chr7:52737058-52742302	Enhancers Weak transcription	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	chr7:52737600-52739000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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