Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10778229	0.90[CEU][hapmap];0.87[EUR][1000 genomes]
rs10860978	0.95[CEU][hapmap]
rs11111510	0.95[CEU][hapmap];0.81[CHD][hapmap];0.82[GIH][hapmap]
rs12311525	0.90[CEU][hapmap];0.81[CHD][hapmap];0.82[GIH][hapmap];0.81[MEX][hapmap];0.90[TSI][hapmap];0.90[EUR][1000 genomes]
rs12578952	0.87[EUR][1000 genomes]
rs1464321	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs1520190	0.90[CEU][hapmap];0.83[EUR][1000 genomes]
rs1520191	0.84[CEU][hapmap];0.82[EUR][1000 genomes]
rs1915110	0.95[CEU][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2373979	0.90[CEU][hapmap];0.83[EUR][1000 genomes]
rs2374053	0.89[MEX][hapmap];0.90[TSI][hapmap];0.87[EUR][1000 genomes]
rs2888710	0.90[EUR][1000 genomes]
rs4379920	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6419384	0.94[CEU][hapmap];0.80[JPT][hapmap];0.92[YRI][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6539064	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs6539066	0.81[CEU][hapmap]
rs7134630	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];0.86[LWK][hapmap];0.85[MEX][hapmap];0.85[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7305590	0.83[EUR][1000 genomes]
rs7308188	0.94[CEU][hapmap];0.85[YRI][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7488867	0.94[ASW][hapmap];0.85[CEU][hapmap];0.83[MKK][hapmap];0.95[TSI][hapmap];0.85[YRI][hapmap];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv455703	chr12:103692799-103818049	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv560037	chr12:103692799-103818049	Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103707200-103786400	Weak transcription	Primary B cells from cord blood	blood
2	chr12:103712600-103734800	Weak transcription	Primary B cells from peripheral blood	blood
3	chr12:103722200-103725800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:103723000-103725800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr12:103723200-103727600	Weak transcription	Fetal Brain Male	brain

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