Variant report

Variant	rs61929389
Chromosome Location	chr12:86320558-86320559
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs61929365	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61929367	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61930914	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61930921	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61930925	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61930957	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61931135	0.96[AMR][1000 genomes]
rs73177158	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73177167	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73177169	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73187654	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv1797806	chr12:86198935-86425608	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv559667	chr12:86318004-86416212	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island 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	chr12:86318600-86324600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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