Variant report

Variant	rs66663059
Chromosome Location	chr15:41462486-41462487
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10152631	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11070323	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17718117	0.85[EUR][1000 genomes]
rs28459903	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28510224	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28523607	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57126801	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58330134	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58547976	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58677271	0.84[EUR][1000 genomes]
rs58819307	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59926382	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61592157	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61648937	0.81[EUR][1000 genomes]
rs66520648	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66723852	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs66993182	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67259166	0.86[EUR][1000 genomes]
rs67891871	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs68180828	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7166556	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7178739	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72737761	0.82[EUR][1000 genomes]
rs73396323	0.97[EUR][1000 genomes]
rs73402954	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv569229	chr15:41361138-41483682	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv904107	chr15:41361138-41493013	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv569230	chr15:41384649-41483682	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv904108	chr15:41384649-41486990	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
5	nsv904109	chr15:41410705-41481254	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv457120	chr15:41410705-41546631	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv569231	chr15:41410705-41546631	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41459800-41463000	Enhancers	Fetal Brain Male	brain
2	chr15:41460400-41462600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr15:41461200-41462600	Enhancers	Monocytes-CD14+_RO01746	blood

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