Variant report

Variant	rs74016519
Chromosome Location	chr15:56860642-56860643
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11630066	1.00[EUR][1000 genomes]
rs11630471	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11631238	1.00[EUR][1000 genomes]
rs11637714	1.00[EUR][1000 genomes]
rs11638781	1.00[EUR][1000 genomes]
rs1711488	1.00[EUR][1000 genomes]
rs58108332	1.00[EUR][1000 genomes]
rs58661360	1.00[EUR][1000 genomes]
rs59270467	1.00[EUR][1000 genomes]
rs59480187	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60623475	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61391531	1.00[EUR][1000 genomes]
rs7163771	1.00[EUR][1000 genomes]
rs7168320	1.00[EUR][1000 genomes]
rs7169816	1.00[EUR][1000 genomes]
rs7171060	1.00[EUR][1000 genomes]
rs7174112	1.00[EUR][1000 genomes]
rs7176311	1.00[EUR][1000 genomes]
rs7176960	1.00[EUR][1000 genomes]
rs7179204	1.00[EUR][1000 genomes]
rs7181220	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73419877	1.00[EUR][1000 genomes]
rs73419878	1.00[EUR][1000 genomes]
rs73421980	1.00[EUR][1000 genomes]
rs73421983	1.00[EUR][1000 genomes]
rs73421988	1.00[EUR][1000 genomes]
rs959631	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1545	chr15:56659498-56897381	Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv471330	chr15:56659709-56896385	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv471506	chr15:56659709-56896385	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv498847	chr15:56667038-56896395	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2525559	chr15:56669294-56897412	Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv3693203	chr15:56676457-56894478	Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv35150	chr15:56677730-56896304	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1049240	chr15:56820899-56890478	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	esv12125	chr15:56851808-56868691	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56860000-56861400	ZNF genes & repeats	Fetal Thymus	thymus
2	chr15:56860000-56861600	ZNF genes & repeats	Thymus	Thymus
3	chr15:56860400-56861600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:56860600-56861400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr15:56860600-56861600	Enhancers	HMEC	breast
6	chr15:56860600-56861800	Enhancers	Dnd41	blood

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