Variant report

Variant	rs61949045
Chromosome Location	chr12:86641690-86641691
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs12299950	0.80[AFR][1000 genomes]
rs12303146	0.80[AFR][1000 genomes]
rs12304593	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs12305255	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12305480	0.80[AFR][1000 genomes]
rs12306726	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12308711	0.80[AFR][1000 genomes]
rs12311208	0.80[AFR][1000 genomes]
rs12316480	0.92[AMR][1000 genomes]
rs12318124	0.80[AFR][1000 genomes]
rs12318727	0.80[AFR][1000 genomes]
rs1389296	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17288772	0.89[AMR][1000 genomes]
rs17289052	0.84[AMR][1000 genomes]
rs17359446	0.97[AMR][1000 genomes]
rs17367374	0.84[AMR][1000 genomes]
rs55649116	0.92[AMR][1000 genomes]
rs55733909	0.92[AMR][1000 genomes]
rs55820226	0.87[AMR][1000 genomes]
rs55832610	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs55886852	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55956857	0.86[AMR][1000 genomes]
rs55998036	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57624840	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58024273	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs59623111	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61932270	0.81[EUR][1000 genomes]
rs61932271	0.81[EUR][1000 genomes]
rs61932272	0.81[EUR][1000 genomes]
rs61932274	0.81[EUR][1000 genomes]
rs61932275	0.81[EUR][1000 genomes]
rs61948967	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61948994	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61949011	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61949013	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61949036	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61949037	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61949038	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61949039	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61949041	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61949047	0.94[AMR][1000 genomes]
rs61949048	0.91[AMR][1000 genomes]
rs61949049	0.91[AMR][1000 genomes]
rs61950663	0.91[AMR][1000 genomes]
rs61950665	0.91[AMR][1000 genomes]
rs61950667	0.86[AMR][1000 genomes]
rs61950671	0.86[AMR][1000 genomes]
rs61950674	0.86[AMR][1000 genomes]
rs61950706	0.83[AMR][1000 genomes]
rs61950711	0.89[AMR][1000 genomes]
rs61950712	0.87[AMR][1000 genomes]
rs61950713	0.89[AMR][1000 genomes]
rs61950746	0.82[AMR][1000 genomes]
rs61950747	0.82[AMR][1000 genomes]
rs61950748	0.82[AMR][1000 genomes]
rs61950749	0.82[AMR][1000 genomes]
rs767898	0.97[AMR][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	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2761759	chr12:86415936-86747726	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv518059	chr12:86416212-86747726	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1041397	chr12:86438607-86737558	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1053087	chr12:86569126-86733418	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv541564	chr12:86569126-86733418	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1037003	chr12:86610040-86798121	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1045386	chr12:86616015-86733418	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv541565	chr12:86616015-86733418	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86641200-86644600	Enhancers	Fetal Heart	heart

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