Variant report

Variant	rs12095985
Chromosome Location	chr1:194123339-194123340
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10921513	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10921523	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10921526	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12057425	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12057943	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12065894	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12066981	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12072567	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12075017	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12076932	0.95[ASN][1000 genomes]
rs12080723	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12082464	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12090496	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12095375	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16836486	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16836610	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59157004	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60096291	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9661433	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9662046	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008266	chr1:193550185-194481053	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv872834	chr1:193889533-194482304	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1001872	chr1:194030479-194288016	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv872836	chr1:194032486-194130204	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv832181	chr1:194089117-194255615	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv872837	chr1:194106280-194221509	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region lncRNA	2 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	chr1:194123000-194123400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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