Variant report

Variant	rs7335074
Chromosome Location	chr13:67148362-67148363
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 122 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10507739	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs11148709	0.83[CHB][hapmap];0.81[JPT][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12868544	0.96[ASN][1000 genomes]
rs12868791	0.89[CHB][hapmap];0.82[ASN][1000 genomes]
rs12868964	0.89[CHB][hapmap];0.82[ASN][1000 genomes]
rs12869171	0.82[ASN][1000 genomes]
rs12877241	0.81[JPT][hapmap]
rs17081458	0.82[ASN][1000 genomes]
rs17081462	0.82[ASN][1000 genomes]
rs17081473	0.82[ASN][1000 genomes]
rs1932881	0.89[CHB][hapmap];0.82[ASN][1000 genomes]
rs1932886	0.89[CHB][hapmap];0.82[ASN][1000 genomes]
rs2184841	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2324915	0.89[CHB][hapmap];0.82[ASN][1000 genomes]
rs2324917	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34038924	0.96[ASN][1000 genomes]
rs34557527	0.96[ASN][1000 genomes]
rs34979741	0.82[ASN][1000 genomes]
rs35049183	0.96[ASN][1000 genomes]
rs35898401	0.96[ASN][1000 genomes]
rs4242928	0.81[ASN][1000 genomes]
rs4379952	0.81[JPT][hapmap]
rs4516088	0.82[ASN][1000 genomes]
rs4883779	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs4883780	0.83[ASN][1000 genomes]
rs4883781	0.83[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4884677	0.86[CHB][hapmap]
rs4884678	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs55774405	0.83[ASN][1000 genomes]
rs56729791	0.83[ASN][1000 genomes]
rs61955971	0.82[ASN][1000 genomes]
rs67609817	0.82[ASN][1000 genomes]
rs7319523	0.82[JPT][hapmap];0.89[YRI][hapmap]
rs7327487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs7332539	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7336189	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs7981496	0.85[ASN][1000 genomes]
rs7984453	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs7984900	0.83[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7986003	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.96[ASN][1000 genomes]
rs7998584	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9317595	0.89[CHB][hapmap];0.85[ASN][1000 genomes]
rs9317596	0.94[CHB][hapmap];0.86[JPT][hapmap]
rs9529076	0.80[CEU][hapmap];0.81[CHB][hapmap];0.81[JPT][hapmap]
rs9529077	0.81[JPT][hapmap]
rs9529081	0.81[JPT][hapmap];0.81[AMR][1000 genomes]
rs9529083	0.81[JPT][hapmap]
rs9529084	0.81[JPT][hapmap]
rs9529086	0.82[ASN][1000 genomes]
rs9529087	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs9529092	0.83[ASN][1000 genomes]
rs9529096	0.89[ASN][1000 genomes]
rs9529098	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs9540772	0.81[JPT][hapmap]
rs9540784	0.81[JPT][hapmap]
rs9540785	0.82[JPT][hapmap]
rs9540786	0.82[JPT][hapmap]
rs9540787	0.82[JPT][hapmap]
rs9540791	0.81[JPT][hapmap]
rs9540794	0.82[ASN][1000 genomes]
rs9540795	0.82[ASN][1000 genomes]
rs9540796	0.89[CHB][hapmap];0.81[ASN][1000 genomes]
rs9540799	0.88[CHB][hapmap];0.83[ASN][1000 genomes]
rs9540800	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs9540801	0.83[ASN][1000 genomes]
rs9540802	0.83[ASN][1000 genomes]
rs9540803	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs9540804	0.89[CHB][hapmap]
rs9540809	0.89[CHB][hapmap]
rs9540810	0.83[ASN][1000 genomes]
rs9540812	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs9540813	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs9540817	0.88[CHB][hapmap];0.82[ASN][1000 genomes]
rs9540821	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.96[ASN][1000 genomes]
rs9540824	1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap];0.97[ASN][1000 genomes]
rs9540826	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9540827	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9540828	0.84[CHB][hapmap];0.84[YRI][hapmap]
rs9540836	0.84[CHB][hapmap];0.81[JPT][hapmap]
rs9564319	0.81[CEU][hapmap]
rs9564320	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs9564321	0.83[CHB][hapmap];0.85[ASN][1000 genomes]
rs9564322	0.85[ASN][1000 genomes]
rs9571595	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs9571596	0.89[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053763	chr13:66210166-67184972	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv541811	chr13:66210166-67184972	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv932195	chr13:66215786-67215733	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv530723	chr13:66219650-67200316	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv1052017	chr13:66232288-67213033	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv915828	chr13:66544825-67212201	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv1041133	chr13:66723731-67530595	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
8	esv2422196	chr13:67041890-67295480	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv832639	chr13:67049800-67223701	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv900392	chr13:67080274-67166073	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv900393	chr13:67080274-67180045	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv900394	chr13:67090292-67180045	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv900395	chr13:67091922-67180045	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv1048897	chr13:67093805-67175675	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv1044410	chr13:67094314-67148488	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv900396	chr13:67095885-67166073	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv900397	chr13:67095885-67180045	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv471142	chr13:67098374-67169478	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv455923	chr13:67098375-67150760	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv562098	chr13:67098375-67150760	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv455924	chr13:67098375-67169478	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv455925	chr13:67098375-67169478	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv562099	chr13:67098375-67169478	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv455926	chr13:67098375-67200654	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
25	nsv562100	chr13:67098375-67200654	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
26	nsv455927	chr13:67098855-67169478	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
27	nsv562101	chr13:67098855-67169478	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
28	nsv1048293	chr13:67099206-67166073	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
29	esv2761797	chr13:67099218-67166073	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
30	nsv1047112	chr13:67103902-67166419	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
31	nsv541813	chr13:67103902-67166419	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
32	nsv1037855	chr13:67104372-67168370	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
33	nsv541814	chr13:67104372-67168370	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
34	nsv1052817	chr13:67104372-67175675	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
35	nsv541815	chr13:67104372-67175675	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
36	nsv530605	chr13:67126136-67697306	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
37	nsv974212	chr13:67131313-67184740	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	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	chr13:67148200-67148800	Enhancers	HSMM	muscle

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