Variant report

Variant	rs6922669
Chromosome Location	chr6:86767255-86767256
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 15 )

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs12214536	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1337854	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1415749	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4312955	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9353362	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	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
4	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
5	nsv1021292	chr6:86611922-86778912	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv1027719	chr6:86745200-87326311	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1026234	chr6:86745200-87640200	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv532046	chr6:86754494-87615799	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:15)

SNP	Gene	Cis/trans	Tissue	Source
rs6922669	SNHG5	Cis_1M	lymphoblastoid	RTeQTL
rs6922669	SNHG5	cis	Heart Left Ventricle	GTEx
rs6922669	SNHG5	cis	Artery Aorta	GTEx
rs6922669	SNHG5	cis	Stomach	GTEx
rs6922669	SNHG5	cis	Esophagus Mucosa	GTEx
rs6922669	SNHG5	cis	Artery Tibial	GTEx
rs6922669	SNHG5	cis	Esophagus Muscularis	GTEx
rs6922669	SNHG5	cis	Whole Blood	GTEx
rs6922669	SNHG5	cis	Adipose Subcutaneous	GTEx
rs6922669	SNHG5	cis	Skin Sun Exposed Lower leg	GTEx
rs6922669	SNHG5	cis	Muscle Skeletal	GTEx
rs6922669	SNHG5	cis	Thyroid	GTEx
rs6922669	SNHG5	cis	Nerve Tibial	GTEx
rs6922669	SNHG5	cis	lung	GTEx
rs6922669	NT5E	cis	Thyroid	GTEx

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:86766800-86767400	Active TSS	HUES48 Cell Line	embryonic stem cell
2	chr6:86766800-86767600	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr6:86766800-86767800	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr6:86766800-86767800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:86766800-86768000	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr6:86767200-86767400	Active TSS	H9 Cell Line	embryonic stem cell
7	chr6:86767200-86767400	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr6:86767200-86767400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:86767200-86767600	Flanking Active TSS	H1 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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