Variant report

Variant	rs280379
Chromosome Location	chr12:41459908-41459909
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1434686	1.00[EUR][1000 genomes]
rs1655670	0.88[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs1675476	0.86[EUR][1000 genomes]
rs1797980	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1797982	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1797999	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs1836304	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs185775	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs1903426	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs280363	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs280369	0.86[EUR][1000 genomes]
rs280373	0.86[EUR][1000 genomes]
rs280376	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs280377	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs280378	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs3905593	0.86[EUR][1000 genomes]
rs396673	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs436655	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs443847	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs447889	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs448780	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs486730	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs486737	0.90[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs491015	0.86[EUR][1000 genomes]
rs492550	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs514247	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs533681	0.86[EUR][1000 genomes]
rs533789	0.93[AFR][1000 genomes]
rs534783	0.86[EUR][1000 genomes]
rs567561	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs577213	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs580942	0.86[EUR][1000 genomes]
rs690895	0.91[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs691482	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs691730	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs691737	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs692016	0.93[AFR][1000 genomes]
rs692143	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs692148	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs692639	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs692665	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs776883	0.86[EUR][1000 genomes]
rs776884	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs776891	0.86[EUR][1000 genomes]
rs776895	0.86[EUR][1000 genomes]
rs776896	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7957386	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs989148	0.86[EUR][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	nsv497867	chr12:41286305-41728650	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv832382	chr12:41359550-41489681	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv427910	chr12:41374913-41650593	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv428587	chr12:41375635-41546845	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1051524	chr12:41409977-41643387	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41429000-41469600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr12:41455400-41462000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr12:41458000-41469600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:41458000-41474000	Weak transcription	Ovary	ovary
5	chr12:41459600-41463600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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