Variant report

Variant	rs6560520
Chromosome Location	chr9:79049340-79049341
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10121699	0.83[ASN][1000 genomes]
rs10124695	0.84[ASN][1000 genomes]
rs10781361	0.86[ASN][1000 genomes]
rs10781362	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11144898	0.87[ASN][1000 genomes]
rs11144899	0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11788095	0.82[ASN][1000 genomes]
rs1535845	0.84[ASN][1000 genomes]
rs2490572	0.90[EUR][1000 genomes]
rs2501937	0.91[EUR][1000 genomes]
rs2501938	0.91[EUR][1000 genomes]
rs4745544	0.84[ASN][1000 genomes]
rs4745548	0.99[ASN][1000 genomes]
rs4745549	0.85[ASN][1000 genomes]
rs6560519	1.00[ASN][1000 genomes]
rs6560521	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6560522	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7038837	0.96[ASN][1000 genomes]
rs7847608	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869152	chr9:78742197-79583399	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv931033	chr9:78850330-79366454	Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv893478	chr9:78933874-79101006	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv893479	chr9:78971253-79275226	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	esv3451027	chr9:79021447-79056132	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv520423	chr9:79047117-79065299	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:79047400-79049400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:79048000-79049400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr9:79048000-79049400	Enhancers	NH-A	brain
4	chr9:79048000-79049400	Enhancers	Osteobl	bone
5	chr9:79048200-79049400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:79048400-79049400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:79048600-79049400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr9:79049200-79050200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr9:79049200-79050200	Weak transcription	HepG2	liver
10	chr9:79049200-79050400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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

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