Variant report

Variant	rs723402
Chromosome Location	chr6:74114591-74114592
allele	C/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:13)

rs_ID	r²[population]
rs11961187	0.85[AMR][1000 genomes]
rs11964808	0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12662148	0.98[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12663695	0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12665048	0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16883692	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2280286	0.81[AMR][1000 genomes]
rs3734512	0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3734516	0.98[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs3757107	0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs930806	0.96[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs930807	0.96[AMR][1000 genomes]
rs930808	0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3410973	chr6:73716033-74419545	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv830693	chr6:74049342-74216080	Flanking Active TSS Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 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	chr6:74105400-74117200	Weak transcription	Placenta	Placenta

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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