Variant report

Variant	rs17357025
Chromosome Location	chr12:86535384-86535385
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10506927	0.92[CEU][hapmap]
rs10506928	1.00[CEU][hapmap]
rs10506931	0.91[CEU][hapmap]
rs10779233	0.92[CEU][hapmap]
rs10863163	0.93[CEU][hapmap]
rs12298174	0.92[CEU][hapmap]
rs12305255	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs12306726	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs12307279	0.83[CEU][hapmap]
rs12308575	0.91[CEU][hapmap]
rs12313444	0.92[CEU][hapmap]
rs12321159	0.92[CEU][hapmap]
rs1389296	0.93[CEU][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1552840	0.85[CEU][hapmap]
rs17284129	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17284484	1.00[CEU][hapmap]
rs17284624	0.92[CEU][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17284820	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17285589	0.85[CEU][hapmap]
rs17357233	0.93[CEU][hapmap]
rs17357259	0.91[CEU][hapmap]
rs17357469	0.92[CEU][hapmap]
rs4586245	0.86[CEU][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4842454	0.91[CEU][hapmap]
rs4842468	0.85[CEU][hapmap]
rs4842541	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4842557	0.85[CEU][hapmap]
rs4842558	0.91[CEU][hapmap]
rs55832610	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55886852	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55998036	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56154427	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57624840	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs58024273	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs59623111	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61931157	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61932264	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61932265	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61932266	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61932268	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61932269	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61932270	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61932271	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61932272	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61932274	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61932275	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61948967	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61948994	0.83[EUR][1000 genomes]
rs61949013	0.83[EUR][1000 genomes]
rs61949036	0.83[EUR][1000 genomes]
rs61949037	0.83[EUR][1000 genomes]
rs61949039	0.81[EUR][1000 genomes]
rs7136697	0.93[CEU][hapmap]
rs7486522	0.93[CEU][hapmap]
rs7487426	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.90[EUR][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	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	nsv470311	chr12:86484366-86550783	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3442004	chr12:86514695-86599965	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv2753278	chr12:86522507-86555154	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86529800-86538800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr12:86530400-86538800	Weak transcription	Brain Germinal Matrix	brain
3	chr12:86532800-86538000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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