Variant report

Variant	rs1797982
Chromosome Location	chr12:41431846-41431847
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10506181	0.97[ASN][1000 genomes]
rs11832384	0.80[ASN][1000 genomes]
rs11834513	0.95[ASN][1000 genomes]
rs1434686	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1442191	0.80[ASN][1000 genomes]
rs1655670	0.86[EUR][1000 genomes]
rs1675476	0.86[EUR][1000 genomes]
rs17128987	0.83[ASN][1000 genomes]
rs17128997	0.97[ASN][1000 genomes]
rs1797980	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1797999	0.86[EUR][1000 genomes]
rs1836304	0.86[EUR][1000 genomes]
rs185775	0.86[EUR][1000 genomes]
rs1903426	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs280363	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs280369	0.86[EUR][1000 genomes]
rs280373	0.86[EUR][1000 genomes]
rs280376	0.86[EUR][1000 genomes]
rs280377	0.86[EUR][1000 genomes]
rs280378	0.86[EUR][1000 genomes]
rs280379	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3905593	0.86[EUR][1000 genomes]
rs396673	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs436655	0.86[EUR][1000 genomes]
rs443847	0.86[EUR][1000 genomes]
rs447889	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs448780	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs486730	0.86[EUR][1000 genomes]
rs486737	0.86[EUR][1000 genomes]
rs491015	0.86[EUR][1000 genomes]
rs492550	0.86[EUR][1000 genomes]
rs514247	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs533681	0.86[EUR][1000 genomes]
rs534783	0.86[EUR][1000 genomes]
rs55927654	0.83[ASN][1000 genomes]
rs55994689	0.97[ASN][1000 genomes]
rs56333303	0.97[ASN][1000 genomes]
rs567561	0.86[EUR][1000 genomes]
rs577213	0.86[EUR][1000 genomes]
rs580942	0.86[EUR][1000 genomes]
rs690895	0.86[EUR][1000 genomes]
rs691482	0.86[EUR][1000 genomes]
rs691730	0.86[EUR][1000 genomes]
rs691737	0.86[EUR][1000 genomes]
rs692143	0.86[EUR][1000 genomes]
rs692148	0.86[EUR][1000 genomes]
rs692639	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs692665	0.86[EUR][1000 genomes]
rs73116958	0.83[ASN][1000 genomes]
rs73116975	0.97[ASN][1000 genomes]
rs73116987	0.97[ASN][1000 genomes]
rs776883	0.86[EUR][1000 genomes]
rs776884	0.86[EUR][1000 genomes]
rs776891	0.86[EUR][1000 genomes]
rs776895	0.86[EUR][1000 genomes]
rs776896	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7957386	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs989148	0.83[AFR][1000 genomes];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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41408200-41449800	Weak transcription	Brain Anterior Caudate	brain
2	chr12:41409000-41435000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:41429000-41469600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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