Variant report

Variant	rs11513891
Chromosome Location	chr12:105696251-105696252
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10861371	0.83[AMR][1000 genomes]
rs10861388	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10861396	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11112451	1.00[ASN][1000 genomes]
rs11112461	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11112465	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11112467	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11112468	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11519725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11613789	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12822081	0.83[AMR][1000 genomes]
rs12822314	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12827086	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12828874	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35225620	0.83[AMR][1000 genomes]
rs35407439	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35561158	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35801994	0.81[AMR][1000 genomes]
rs4545651	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7303242	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7303307	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7959385	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7972400	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7972676	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7972982	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899499	chr12:105616297-105722529	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv510589	chr12:105670071-105743755	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3394212	chr12:105693734-105708035	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
4	esv3358347	chr12:105693757-105707693	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	lncRNA	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	chr12:105692200-105703600	Weak transcription	A549	lung
2	chr12:105692200-105708000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr12:105695400-105708200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr12:105695800-105709200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr12:105696200-105701200	Weak transcription	HUVEC	blood vessel
6	chr12:105696200-105709400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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