Variant report

Variant	rs274632
Chromosome Location	chr7:86269181-86269182
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10227921	1.00[CHB][hapmap]
rs10257201	1.00[CHB][hapmap]
rs11762187	1.00[CHB][hapmap]
rs12704282	1.00[CHB][hapmap]
rs13242038	1.00[CHB][hapmap]
rs1527762	1.00[CHB][hapmap]
rs2282960	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2299218	1.00[CHB][hapmap]
rs274635	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs701332	1.00[CHB][hapmap]
rs724224	0.84[ASN][1000 genomes]
rs724927	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7806940	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs802425	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs802432	1.00[CHB][hapmap]
rs802467	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs802478	0.82[EUR][1000 genomes];0.86[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	nsv1025032	chr7:86032479-86642973	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv831053	chr7:86268171-86440999	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86267000-86272600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr7:86267400-86269400	Enhancers	Brain Hippocampus Middle	brain
3	chr7:86268000-86271600	Weak transcription	Brain Angular Gyrus	brain
4	chr7:86268600-86269600	Enhancers	Brain Substantia Nigra	brain
5	chr7:86268800-86269200	Enhancers	Brain Cingulate Gyrus	brain
6	chr7:86268800-86269600	Enhancers	Brain Anterior Caudate	brain

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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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