Variant report

Variant	rs4561528
Chromosome Location	chr17:17979099-17979100
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:17972487..17976143-chr17:17976511..17979326,5	K562	blood:
2	chr17:17973806..17976094-chr17:17976515..17979331,5	K562	blood:

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs1008135	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1101727	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11078410	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11650021	0.83[EUR][1000 genomes]
rs11867241	0.86[EUR][1000 genomes]
rs12939020	0.82[EUR][1000 genomes]
rs2056842	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2955350	0.84[EUR][1000 genomes]
rs2955353	0.84[EUR][1000 genomes]
rs2955354	0.84[EUR][1000 genomes]
rs2955355	0.84[EUR][1000 genomes]
rs2955356	0.84[EUR][1000 genomes]
rs2955357	0.84[EUR][1000 genomes]
rs2955358	0.84[EUR][1000 genomes]
rs2955359	0.84[EUR][1000 genomes]
rs2955365	0.94[EUR][1000 genomes]
rs2955366	0.94[EUR][1000 genomes]
rs2955367	0.83[EUR][1000 genomes]
rs2955368	0.85[EUR][1000 genomes]
rs2955370	0.84[EUR][1000 genomes]
rs2955372	0.85[EUR][1000 genomes]
rs2955380	0.83[EUR][1000 genomes]
rs2955381	0.82[EUR][1000 genomes]
rs2955383	0.83[EUR][1000 genomes]
rs2955384	0.82[EUR][1000 genomes]
rs2955385	0.82[EUR][1000 genomes]
rs2974998	0.94[EUR][1000 genomes]
rs2974999	0.93[EUR][1000 genomes]
rs4365346	0.93[EUR][1000 genomes]
rs4410135	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4426402	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4506967	0.89[EUR][1000 genomes]
rs4643387	0.85[EUR][1000 genomes]
rs4925135	0.83[EUR][1000 genomes]
rs4925136	0.84[EUR][1000 genomes]
rs59518074	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62073573	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6502633	0.82[EUR][1000 genomes]
rs6502634	0.82[EUR][1000 genomes]
rs6502636	0.94[EUR][1000 genomes]
rs6502637	0.93[EUR][1000 genomes]
rs6826	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs712267	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs712268	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7207461	0.84[EUR][1000 genomes]
rs7210400	0.84[EUR][1000 genomes]
rs7211714	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7212447	0.93[EUR][1000 genomes]
rs721669	0.92[EUR][1000 genomes]
rs7224047	0.81[EUR][1000 genomes]
rs7406744	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7406982	0.81[EUR][1000 genomes]
rs741782	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7503738	0.81[EUR][1000 genomes]
rs8066764	0.93[EUR][1000 genomes]
rs8080602	0.84[EUR][1000 genomes]
rs854763	0.92[EUR][1000 genomes]
rs854767	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs854768	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs854769	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs854770	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs854789	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs854790	0.93[EUR][1000 genomes]
rs854791	0.91[EUR][1000 genomes]
rs854808	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs854809	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs854814	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs854817	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs854818	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9303144	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9894138	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv533142	chr17:17691726-18236686	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
4	nsv482879	chr17:17802463-17989273	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv960429	chr17:17951047-18027679	Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	nsv482491	chr17:17959577-18153920	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	nsv1061162	chr17:17978838-18259234	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 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	chr17:17974600-17979200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr17:17974600-17984400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr17:17974600-17986400	Weak transcription	Placenta	Placenta
4	chr17:17978800-17980800	Enhancers	HepG2	liver
5	chr17:17979000-17982400	Weak transcription	K562	blood

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