Variant report

Variant	rs1906787
Chromosome Location	chr14:46120938-46120939
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10134999	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10145843	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1686235	0.95[EUR][1000 genomes]
rs17116250	0.85[EUR][1000 genomes]
rs17116251	0.85[EUR][1000 genomes]
rs17116252	0.85[EUR][1000 genomes]
rs17116269	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17116271	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17116287	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17116303	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17116352	0.88[EUR][1000 genomes]
rs17116364	0.90[EUR][1000 genomes]
rs17116377	0.88[EUR][1000 genomes]
rs17116385	0.91[EUR][1000 genomes]
rs1750087	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1906789	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1906799	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1906809	0.90[EUR][1000 genomes]
rs2093412	0.87[CEU][hapmap]
rs2250214	0.90[EUR][1000 genomes]
rs2297998	0.90[EUR][1000 genomes]
rs28522365	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28835981	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28872244	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4624080	0.87[EUR][1000 genomes]
rs56799770	0.98[EUR][1000 genomes]
rs56922080	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs57434363	0.88[EUR][1000 genomes]
rs57969791	0.90[EUR][1000 genomes]
rs59944893	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61019014	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61071649	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73343512	0.90[EUR][1000 genomes]
rs73343514	0.90[EUR][1000 genomes]
rs73343516	0.90[EUR][1000 genomes]
rs73343519	0.90[EUR][1000 genomes]
rs73345722	0.89[EUR][1000 genomes]
rs73345726	0.88[EUR][1000 genomes]
rs73359414	0.96[EUR][1000 genomes]
rs73359417	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73359422	0.93[EUR][1000 genomes]
rs73359438	0.98[EUR][1000 genomes]
rs73359460	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8005289	0.90[EUR][1000 genomes]
rs946994	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs946995	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530814	chr14:45604432-46198418	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1042989	chr14:45774194-46489107	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv901847	chr14:45797782-46607899	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2422441	chr14:45848850-46325684	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1035463	chr14:45940562-46201777	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv542083	chr14:45940562-46201777	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv976289	chr14:45973774-46282154	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1044871	chr14:46007760-46432325	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv456282	chr14:46024675-46458696	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv564729	chr14:46024675-46458696	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr14:46120600-46121600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr14:46120800-46121200	Enhancers	Fetal Kidney	kidney
3	chr14:46120800-46121200	Enhancers	HSMM	muscle
4	chr14:46120800-46121800	Enhancers	HMEC	breast

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