Variant report

Variant	rs4574911
Chromosome Location	chr9:72607203-72607204
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:72602857..72604672-chr9:72606319..72607860,2	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1027283	0.99[ASN][1000 genomes]
rs1027284	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10735572	0.93[ASN][1000 genomes]
rs10780718	0.93[ASN][1000 genomes]
rs10780724	0.93[ASN][1000 genomes]
rs10868248	0.84[CHB][hapmap]
rs10868291	0.93[ASN][1000 genomes]
rs10868299	0.94[ASN][1000 genomes]
rs10868327	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10868358	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10868378	0.88[ASN][1000 genomes]
rs1121607	0.93[ASN][1000 genomes]
rs1121608	0.93[ASN][1000 genomes]
rs1389125	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1473520	0.92[ASN][1000 genomes]
rs1493046	0.90[ASN][1000 genomes]
rs1493047	0.93[ASN][1000 genomes]
rs1542769	0.99[ASN][1000 genomes]
rs1586914	0.93[ASN][1000 genomes]
rs1873825	0.96[ASN][1000 genomes]
rs1907956	0.93[ASN][1000 genomes]
rs1907959	0.93[ASN][1000 genomes]
rs1976234	0.82[ASN][1000 genomes]
rs2035922	0.96[ASN][1000 genomes]
rs2975859	0.88[ASN][1000 genomes]
rs2975860	0.88[ASN][1000 genomes]
rs2975926	0.87[ASN][1000 genomes]
rs3015226	0.89[ASN][1000 genomes]
rs4403478	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4413835	0.81[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs4418399	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4445287	1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs4487845	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4490905	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4636269	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4744583	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4744584	0.89[ASN][1000 genomes]
rs6559854	0.83[ASN][1000 genomes]
rs7019025	0.96[ASN][1000 genomes]
rs7023406	0.87[ASN][1000 genomes]
rs7025044	0.93[ASN][1000 genomes]
rs7029606	0.93[ASN][1000 genomes]
rs7035415	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7037671	0.93[ASN][1000 genomes]
rs7847934	0.93[ASN][1000 genomes]
rs7863165	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7863229	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs870011	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs902964	0.97[ASN][1000 genomes]
rs931500	0.92[ASN][1000 genomes]
rs953372	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs996375	0.93[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	nsv893438	chr9:72363992-72720438	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv831612	chr9:72473778-72634253	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1049457	chr9:72539144-72765913	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1035668	chr9:72555053-72632796	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1051004	chr9:72557761-72632015	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv831613	chr9:72586058-72740061	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72597400-72608000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr9:72602600-72610800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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