Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1339255	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1339256	1.00[MEX][hapmap]
rs1416557	1.00[EUR][1000 genomes]
rs175780	1.00[CEU][hapmap]
rs2143550	1.00[CEU][hapmap]
rs2423987	1.00[CEU][hapmap]
rs4814418	1.00[CEU][hapmap];0.88[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4814421	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs6034337	1.00[CEU][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6034338	1.00[EUR][1000 genomes]
rs6043602	1.00[CEU][hapmap]
rs6043624	1.00[CEU][hapmap]
rs6043627	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6043638	1.00[CEU][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6080022	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs6080024	0.89[ASW][hapmap]
rs6131746	1.00[MEX][hapmap]
rs717146	1.00[CEU][hapmap]
rs7352227	1.00[CEU][hapmap];1.00[MEX][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs775094	1.00[CEU][hapmap]
rs775096	1.00[CEU][hapmap]
rs811343	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv833929	chr20:15765372-15977337	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3447866	chr20:15799286-16115291	Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15912000-15930200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr20:15920600-15922400	Weak transcription	Primary B cells from peripheral blood	blood
3	chr20:15921400-15928000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr20:15922000-15922600	Strong transcription	Primary B cells from cord blood	blood

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