Variant report

Variant	rs11183575
Chromosome Location	chr12:47108139-47108140
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10785635	0.81[EUR][1000 genomes]
rs10880987	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10880996	0.88[ASN][1000 genomes]
rs10880997	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11183560	0.85[ASN][1000 genomes]
rs11183561	0.82[EUR][1000 genomes]
rs11183562	0.83[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs11183571	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11183576	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11183600	0.83[ASN][1000 genomes]
rs11610453	0.84[ASN][1000 genomes]
rs11830275	0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12423908	0.86[ASN][1000 genomes]
rs12426014	0.83[ASN][1000 genomes]
rs12426320	0.86[ASN][1000 genomes]
rs12426545	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12426593	0.86[ASN][1000 genomes]
rs180403	0.81[CHD][hapmap]
rs180405	0.83[CHD][hapmap]
rs180409	0.91[CHB][hapmap];0.81[ASN][1000 genomes]
rs180412	0.86[CHB][hapmap]
rs180421	0.83[CHD][hapmap]
rs180427	0.82[CEU][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];0.81[LWK][hapmap];0.83[MEX][hapmap]
rs180429	0.80[CHD][hapmap]
rs180430	0.80[CHD][hapmap]
rs2080687	0.87[ASN][1000 genomes]
rs2111772	0.86[ASN][1000 genomes]
rs2193652	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2408622	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2465582	0.80[CHD][hapmap]
rs2465584	0.83[CHD][hapmap]
rs35813765	0.94[ASN][1000 genomes]
rs35827448	0.94[ASN][1000 genomes]
rs4140781	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4140782	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4768130	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7304808	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7484804	0.81[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7484950	0.86[ASN][1000 genomes]
rs7972141	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049525	chr12:46721742-47264172	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv541486	chr12:46721742-47264172	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
3	esv3416674	chr12:46988689-47178369	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv558783	chr12:46996632-47144856	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv1845143	chr12:47051076-47431496	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11183575	ADAMTS20	cis	parietal	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47103000-47116000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr12:47105200-47111600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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