Variant report

Variant	rs62572583
Chromosome Location	chr9:72585110-72585111
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	chr9:72579585..72583057-chr9:72584421..72588172,5	K562	blood:

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

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10217790	0.92[ASN][1000 genomes]
rs1027282	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10511978	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10868348	0.99[ASN][1000 genomes]
rs11141101	0.99[ASN][1000 genomes]
rs11141106	0.97[ASN][1000 genomes]
rs11141122	0.97[ASN][1000 genomes]
rs11141127	0.80[ASN][1000 genomes]
rs11141246	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11141260	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11788010	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11789512	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11790329	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12336812	0.97[ASN][1000 genomes]
rs12353051	0.97[ASN][1000 genomes]
rs12353052	0.97[ASN][1000 genomes]
rs12551035	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12551904	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12552060	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12554412	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12554849	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12555905	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12683555	0.97[ASN][1000 genomes]
rs12683959	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12686422	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12686803	0.97[ASN][1000 genomes]
rs17442733	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17443354	0.97[ASN][1000 genomes]
rs17522643	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs17522671	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2131427	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2131428	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2172432	0.97[ASN][1000 genomes]
rs2201232	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2220736	0.96[ASN][1000 genomes]
rs2220737	0.97[ASN][1000 genomes]
rs4256644	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56380265	0.97[ASN][1000 genomes]
rs56399669	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs57388366	0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs61210535	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62572585	0.97[ASN][1000 genomes]
rs62572586	0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62572589	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62572598	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62572600	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62572601	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62572604	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs62572605	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs66542913	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7026012	0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7026154	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73456376	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72580000-72586600	Weak transcription	HMEC	breast
2	chr9:72580400-72585400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr9:72580400-72585600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr9:72580400-72585600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr9:72580400-72586400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr9:72580400-72586600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:72580400-72586800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr9:72580400-72590600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:72580600-72591000	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr9:72580800-72586400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr9:72581200-72585800	Weak transcription	NH-A	brain
12	chr9:72581400-72585200	Weak transcription	Osteobl	bone
13	chr9:72581400-72586400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr9:72584200-72591000	Weak transcription	Esophagus	oesophagus
15	chr9:72584400-72585800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr9:72584400-72586600	Enhancers	NHDF-Ad	bronchial
17	chr9:72584400-72587200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr9:72584600-72585200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr9:72584600-72585800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:72584600-72585800	Enhancers	HUVEC	blood vessel
21	chr9:72584800-72585200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr9:72584800-72585600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr9:72584800-72586000	Enhancers	NHLF	lung
24	chr9:72585000-72586400	Weak transcription	Muscle Satellite Cultured Cells	--

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