Variant report

Variant	rs6114875
Chromosome Location	chr20:24788418-24788419
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:24786455..24788540-chr20:24788618..24791423,2	MCF-7	breast:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1109682	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11908480	0.92[EUR][1000 genomes]
rs1467769	0.92[EUR][1000 genomes]
rs2151460	0.92[EUR][1000 genomes]
rs34799975	0.92[EUR][1000 genomes]
rs6036921	0.92[EUR][1000 genomes]
rs6036927	0.92[EUR][1000 genomes]
rs6036932	0.92[EUR][1000 genomes]
rs6036938	0.92[EUR][1000 genomes]
rs6036944	0.92[EUR][1000 genomes]
rs6050001	0.92[EUR][1000 genomes]
rs6050003	0.92[EUR][1000 genomes]
rs6050005	0.92[EUR][1000 genomes]
rs6050006	0.92[EUR][1000 genomes]
rs6050013	0.92[EUR][1000 genomes]
rs6050014	0.92[EUR][1000 genomes]
rs6050016	1.00[EUR][1000 genomes]
rs6050017	0.92[EUR][1000 genomes]
rs6050019	0.92[EUR][1000 genomes]
rs6050023	0.92[EUR][1000 genomes]
rs6050041	0.92[EUR][1000 genomes]
rs6050042	0.92[EUR][1000 genomes]
rs6050045	0.92[EUR][1000 genomes]
rs6050047	0.92[EUR][1000 genomes]
rs6050049	0.92[EUR][1000 genomes]
rs6106952	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6114886	0.92[EUR][1000 genomes]
rs6114888	0.92[EUR][1000 genomes]
rs7262621	0.92[EUR][1000 genomes]
rs7262640	0.92[EUR][1000 genomes]
rs73333473	0.93[AMR][1000 genomes]
rs73335473	0.92[EUR][1000 genomes]
rs73335492	0.92[EUR][1000 genomes]
rs73337274	0.92[EUR][1000 genomes]
rs73339206	1.00[EUR][1000 genomes]
rs73903961	0.92[EUR][1000 genomes]
rs73903963	0.92[EUR][1000 genomes]
rs73903968	0.92[EUR][1000 genomes]
rs8119131	0.92[EUR][1000 genomes]
rs914306	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332519	chr20:24535099-24815615	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1061412	chr20:24629468-24887869	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv544216	chr20:24629468-24887869	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1061281	chr20:24711635-24815107	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv544217	chr20:24711635-24815107	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv912825	chr20:24715544-24813345	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv1061455	chr20:24733120-24861801	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv544218	chr20:24733120-24861801	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	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	chr20:24777200-24791400	Weak transcription	Spleen	Spleen
2	chr20:24783200-24790400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:24787800-24788600	Enhancers	Placenta	Placenta
4	chr20:24788200-24790000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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