Variant report

Variant	rs11004060
Chromosome Location	chr10:55845526-55845527
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10509004	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10825215	0.94[CEU][hapmap];1.00[CHB][hapmap]
rs11004027	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11004028	0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11004029	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11004030	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11004031	0.95[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11004032	0.95[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11004034	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs11004035	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs11004036	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs11004037	0.94[CEU][hapmap];1.00[CHB][hapmap]
rs11004058	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11591621	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs11593843	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs11594564	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[GIH][hapmap];0.93[TSI][hapmap]
rs11594638	0.95[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11595991	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11597389	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs11598849	0.82[CHB][hapmap]
rs11599859	0.94[CEU][hapmap];1.00[CHB][hapmap]
rs12242499	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs12243005	0.89[EUR][1000 genomes]
rs12244555	0.94[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes]
rs12244759	0.87[EUR][1000 genomes]
rs12247878	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs12250607	0.89[EUR][1000 genomes]
rs12250681	0.95[CEU][hapmap];1.00[CHB][hapmap];0.88[EUR][1000 genomes]
rs12251985	0.86[EUR][1000 genomes]
rs12252125	0.88[EUR][1000 genomes]
rs12252197	0.89[EUR][1000 genomes]
rs12253866	0.88[EUR][1000 genomes]
rs12255282	0.94[CEU][hapmap]
rs12256879	0.94[CEU][hapmap];1.00[CHB][hapmap]
rs12256947	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs12257012	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs12257312	0.89[EUR][1000 genomes]
rs12257494	0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12258948	0.88[EUR][1000 genomes]
rs16913805	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs16937895	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16937899	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17636887	0.81[CEU][hapmap];0.82[CHB][hapmap]
rs17643506	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs17643564	0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.89[TSI][hapmap]
rs17644196	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17644321	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs17711275	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs17711455	0.94[CEU][hapmap];1.00[CHB][hapmap]
rs1911379	0.95[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1911401	0.82[CHB][hapmap]
rs1911402	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs2135715	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs2610873	0.95[CEU][hapmap];0.85[CHB][hapmap]
rs2660150	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs2660151	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs2660152	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs2660154	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs2660159	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs28701623	0.88[EUR][1000 genomes]
rs3812657	0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61858410	0.80[EUR][1000 genomes]
rs7097777	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs72794984	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72797006	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797007	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797008	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72797009	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797010	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797011	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797012	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797015	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797020	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797021	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797022	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797023	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7898152	0.95[CEU][hapmap];1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949692	chr10:55502542-55893206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv869303	chr10:55714219-55857931	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv8667	chr10:55803106-56022647	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv428557	chr10:55815334-55988225	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv870252	chr10:55823123-56029435	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv948730	chr10:55845301-56093271	ZNF genes & repeats Enhancers Weak transcription Active TSS 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	chr10:55841400-55847600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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