Variant report

Variant	rs59012225
Chromosome Location	chr6:165405813-165405814
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs12525727	0.86[ASN][1000 genomes]
rs1322200	0.92[ASN][1000 genomes]
rs1322202	0.93[ASN][1000 genomes]
rs1322203	0.93[ASN][1000 genomes]
rs1407369	0.90[ASN][1000 genomes]
rs2025156	0.84[ASN][1000 genomes]
rs28539262	0.97[ASN][1000 genomes]
rs395044	0.86[ASN][1000 genomes]
rs56817740	0.97[ASN][1000 genomes]
rs58019489	1.00[ASN][1000 genomes]
rs60762728	0.97[ASN][1000 genomes]
rs60847295	0.97[ASN][1000 genomes]
rs60940970	1.00[ASN][1000 genomes]
rs61068180	1.00[ASN][1000 genomes]
rs61272650	0.86[ASN][1000 genomes]
rs6455986	0.86[ASN][1000 genomes]
rs6909389	0.93[ASN][1000 genomes]
rs6918075	1.00[ASN][1000 genomes]
rs6930938	0.84[ASN][1000 genomes]
rs6931158	0.86[ASN][1000 genomes]
rs6931320	0.93[ASN][1000 genomes]
rs6931708	0.86[ASN][1000 genomes]
rs6937822	0.92[ASN][1000 genomes]
rs7768646	0.98[ASN][1000 genomes]
rs7770804	0.86[ASN][1000 genomes]
rs7770961	0.86[ASN][1000 genomes]
rs9347058	0.97[ASN][1000 genomes]
rs9347973	0.97[ASN][1000 genomes]
rs9347974	0.97[ASN][1000 genomes]
rs9347975	0.95[ASN][1000 genomes]
rs9347976	0.98[ASN][1000 genomes]
rs9355527	0.98[ASN][1000 genomes]
rs9355530	0.86[ASN][1000 genomes]
rs9356331	0.97[ASN][1000 genomes]
rs9356333	0.98[ASN][1000 genomes]
rs9365845	0.97[ASN][1000 genomes]
rs9365846	0.97[ASN][1000 genomes]
rs9365847	0.98[ASN][1000 genomes]
rs9365848	0.96[ASN][1000 genomes]
rs9365853	0.98[ASN][1000 genomes]
rs9365854	0.96[ASN][1000 genomes]
rs9365856	0.86[ASN][1000 genomes]
rs975009	0.89[ASN][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	nsv886925	chr6:165319631-165705488	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
2	nsv886926	chr6:165358270-165478051	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv886927	chr6:165368163-165644276	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv3410145	chr6:165395590-165416763	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165404200-165406200	Enhancers	Placenta	Placenta
2	chr6:165405000-165406200	Enhancers	Placenta Amnion	Placenta Amnion

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Input of quick search could be:

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

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