Variant report

Variant	rs12070909
Chromosome Location	chr1:195736200-195736201
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10921920	1.00[AMR][1000 genomes]
rs12057377	1.00[AMR][1000 genomes]
rs12058845	1.00[AMR][1000 genomes]
rs12065480	1.00[AMR][1000 genomes]
rs12065832	1.00[AMR][1000 genomes]
rs12071542	1.00[AMR][1000 genomes]
rs12074439	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12077673	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12090999	1.00[AMR][1000 genomes]
rs12097767	1.00[AMR][1000 genomes]
rs28473187	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872894	chr1:195053221-195745968	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv872937	chr1:195493538-195849028	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1007203	chr1:195672857-195902360	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv2762211	chr1:195734313-195741103	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:195736000-195736400	Enhancers	A549	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
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