Variant report

Variant	rs776895
Chromosome Location	chr12:41499344-41499345
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1434686	0.86[EUR][1000 genomes]
rs1655670	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1675476	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1797980	0.86[EUR][1000 genomes]
rs1797982	0.86[EUR][1000 genomes]
rs1797999	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1836304	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs185775	1.00[EUR][1000 genomes]
rs1903426	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs280369	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs280373	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs280376	1.00[EUR][1000 genomes]
rs280377	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs280378	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs280379	0.86[EUR][1000 genomes]
rs3905593	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs396673	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs436655	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs443847	1.00[EUR][1000 genomes]
rs447889	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs448780	0.86[EUR][1000 genomes]
rs473774	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs486730	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs486737	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs491015	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs492550	1.00[EUR][1000 genomes]
rs514247	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs533681	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs533789	0.93[ASN][1000 genomes]
rs534783	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs567561	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs577213	1.00[EUR][1000 genomes]
rs580942	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs690895	1.00[EUR][1000 genomes]
rs691482	1.00[EUR][1000 genomes]
rs691730	1.00[EUR][1000 genomes]
rs691737	1.00[EUR][1000 genomes]
rs692143	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs692148	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs692639	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs692665	1.00[EUR][1000 genomes]
rs776883	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs776884	1.00[EUR][1000 genomes]
rs776891	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs776896	0.86[EUR][1000 genomes]
rs7957386	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs989148	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][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	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	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
3	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
4	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
5	esv3486219	chr12:41494541-41517945	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv3486208	chr12:41494583-41517897	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv3486230	chr12:41494583-41517897	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
8	esv14849	chr12:41494646-41517821	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
9	nsv1048124	chr12:41499221-41585315	Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41498000-41501400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr12:41498000-41502000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr12:41498400-41502200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:41498800-41500200	Weak transcription	Pancreas	Pancrea

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