Variant report

Variant	rs6487744
Chromosome Location	chr12:29183689-29183690
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10743631	0.80[ASN][1000 genomes]
rs10743637	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10743641	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10771460	0.80[ASN][1000 genomes]
rs10771461	0.80[ASN][1000 genomes]
rs10771466	0.89[ASN][1000 genomes]
rs10771467	0.89[ASN][1000 genomes]
rs10771470	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10771471	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10771473	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10771474	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10771475	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10771477	0.87[EUR][1000 genomes]
rs10771478	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10843295	0.89[ASN][1000 genomes]
rs10843303	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10843304	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10843305	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10843306	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10843307	0.87[EUR][1000 genomes]
rs10843308	0.88[EUR][1000 genomes]
rs1344854	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1344855	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1865765	0.81[AMR][1000 genomes]
rs1865766	0.89[ASN][1000 genomes]
rs1865767	0.89[ASN][1000 genomes]
rs2060567	0.89[ASN][1000 genomes]
rs2060568	0.89[ASN][1000 genomes]
rs2099530	0.89[ASN][1000 genomes]
rs2117992	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2117996	0.89[ASN][1000 genomes]
rs2164494	0.89[ASN][1000 genomes]
rs2349571	0.86[ASN][1000 genomes]
rs2349572	0.87[ASN][1000 genomes]
rs4141946	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4471475	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4558201	0.89[ASN][1000 genomes]
rs4583013	0.89[ASN][1000 genomes]
rs4930843	0.89[ASN][1000 genomes]
rs4930848	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4931127	0.89[ASN][1000 genomes]
rs4931135	0.89[ASN][1000 genomes]
rs6487738	0.80[ASN][1000 genomes]
rs6487741	0.89[ASN][1000 genomes]
rs6487742	0.89[ASN][1000 genomes]
rs6487745	0.89[ASN][1000 genomes]
rs6487746	0.89[ASN][1000 genomes]
rs6487749	0.89[ASN][1000 genomes]
rs7136128	0.89[ASN][1000 genomes]
rs7295074	0.88[ASN][1000 genomes]
rs7297486	0.89[ASN][1000 genomes]
rs7301343	0.89[ASN][1000 genomes]
rs7302286	0.81[ASN][1000 genomes]
rs7302810	0.86[ASN][1000 genomes]
rs7303155	0.81[ASN][1000 genomes]
rs7303768	0.80[ASN][1000 genomes]
rs7308854	0.87[ASN][1000 genomes]
rs7311435	0.89[ASN][1000 genomes]
rs7953668	0.81[ASN][1000 genomes]
rs7955393	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7962367	0.89[ASN][1000 genomes]
rs7963989	0.81[ASN][1000 genomes]
rs7964060	0.81[ASN][1000 genomes]
rs7967094	0.81[ASN][1000 genomes]
rs7969043	0.80[ASN][1000 genomes]
rs7978848	0.80[ASN][1000 genomes]
rs7978997	0.89[ASN][1000 genomes]
rs7979959	0.85[ASN][1000 genomes]
rs9300183	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9651801	0.80[ASN][1000 genomes]
rs9651838	0.91[EUR][1000 genomes]
rs9651839	0.80[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	nsv532233	chr12:29009388-29496179	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv995123	chr12:29095272-29571558	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	esv2758301	chr12:29110782-29289849	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2759888	chr12:29110782-29289849	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29183600-29185200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr12:29183600-29188000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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