Variant report

Variant	rs806529
Chromosome Location	chr6:86467121-86467122
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12212151	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13207173	0.80[EUR][1000 genomes]
rs2324817	0.80[EUR][1000 genomes]
rs34522955	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34795473	0.80[EUR][1000 genomes]
rs3966881	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4098044	0.80[EUR][1000 genomes]
rs6454487	0.80[EUR][1000 genomes]
rs6454488	0.80[EUR][1000 genomes]
rs7450035	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs791503	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9647601	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028293	chr6:86353958-86778912	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	100 gene(s)	inside rSNPs	diseases
2	nsv538350	chr6:86353958-86778912	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	100 gene(s)	inside rSNPs	diseases
3	nsv886335	chr6:86445651-86669361	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1022618	chr6:86465365-87432069	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv538352	chr6:86465365-87432069	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs806529	SNHG5	cis	multi-tissue	Pritchard
rs806529	SNHG5	Cis_1M	lymphoblastoid	RTeQTL
rs806529	SNHG5	cis	Esophagus Mucosa	GTEx
rs806529	SNHG5	cis	Thyroid	GTEx
rs806529	SNHG5	cis	Muscle Skeletal	GTEx
rs806529	SNHG5	cis	Whole Blood	GTEx
rs806529	SNHG5	cis	Nerve Tibial	GTEx
rs806529	SNHG5	cis	Artery Tibial	GTEx
rs806529	SNHG5	cis	lung	GTEx
rs806529	SNHG5	cis	Adipose Subcutaneous	GTEx
rs806529	SNHG5	cis	Heart Left Ventricle	GTEx
rs806529	SNHG5	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:0 , 50 per page) page:

No data

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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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