Variant report

Variant	rs66491474
Chromosome Location	chr10:21747315-21747316
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:21745089..21747569-chr10:21821543..21824085,2	K562	blood:

Variant related genes	Relation type
ENSG00000078403	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10082390	0.89[ASN][1000 genomes]
rs11591285	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11592490	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11592821	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11592976	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11593346	0.92[EUR][1000 genomes]
rs11593992	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11594201	0.84[ASN][1000 genomes]
rs11594724	0.89[ASN][1000 genomes]
rs11594786	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11595095	1.00[EUR][1000 genomes]
rs11595127	1.00[EUR][1000 genomes]
rs11595687	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11596452	0.85[ASN][1000 genomes]
rs11597809	1.00[EUR][1000 genomes]
rs16921815	0.87[ASN][1000 genomes]
rs58747541	0.89[ASN][1000 genomes]
rs59897829	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs60417388	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6482181	0.81[ASN][1000 genomes]
rs66585462	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66850655	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs66880231	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs66906877	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs67332292	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs68153488	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7074328	0.80[ASN][1000 genomes]
rs72794816	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7895825	0.84[ASN][1000 genomes]
rs959652	0.81[ASN][1000 genomes]
rs9664320	0.84[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	nsv825284	chr10:21739527-21847437	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
2	nsv825285	chr10:21742026-21874334	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21738600-21762000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr10:21746600-21748000	Enhancers	Fetal Muscle Leg	muscle
3	chr10:21747000-21747600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr10:21747000-21751400	Weak transcription	Fetal Muscle Trunk	muscle
5	chr10:21747200-21747600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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