Variant report

Variant	rs62572585
Chromosome Location	chr9:72592304-72592305
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10217790	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1027282	0.99[ASN][1000 genomes]
rs10511978	0.99[ASN][1000 genomes]
rs10868348	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11141101	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11141106	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11141122	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11141127	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11141246	0.92[ASN][1000 genomes]
rs11141260	0.95[ASN][1000 genomes]
rs11788010	0.99[ASN][1000 genomes]
rs11789512	0.89[ASN][1000 genomes]
rs11790329	0.89[ASN][1000 genomes]
rs12336812	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12353051	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12353052	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12551035	0.95[ASN][1000 genomes]
rs12551904	0.95[ASN][1000 genomes]
rs12552060	0.99[ASN][1000 genomes]
rs12554412	0.88[ASN][1000 genomes]
rs12554849	0.89[ASN][1000 genomes]
rs12555905	0.95[ASN][1000 genomes]
rs12683555	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12683959	0.99[ASN][1000 genomes]
rs12686422	0.99[ASN][1000 genomes]
rs12686803	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17442733	0.97[ASN][1000 genomes]
rs17443354	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17522643	0.89[ASN][1000 genomes]
rs17522671	0.89[ASN][1000 genomes]
rs2131427	0.99[ASN][1000 genomes]
rs2131428	0.99[ASN][1000 genomes]
rs2172432	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2201232	0.99[ASN][1000 genomes]
rs2220736	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2220737	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4256644	0.94[ASN][1000 genomes]
rs56380265	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56399669	0.95[ASN][1000 genomes]
rs57388366	0.93[ASN][1000 genomes]
rs61210535	0.99[ASN][1000 genomes]
rs62572583	0.97[ASN][1000 genomes]
rs62572586	0.99[ASN][1000 genomes]
rs62572589	0.99[ASN][1000 genomes]
rs62572598	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs62572600	0.95[ASN][1000 genomes]
rs62572601	0.97[ASN][1000 genomes]
rs62572604	0.89[ASN][1000 genomes]
rs62572605	0.89[ASN][1000 genomes]
rs66542913	0.89[ASN][1000 genomes]
rs7026012	0.99[ASN][1000 genomes]
rs7026154	0.99[ASN][1000 genomes]
rs73456376	0.89[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:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72587000-72596800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr9:72590000-72592400	Enhancers	NH-A	brain
3	chr9:72590400-72592400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr9:72591200-72594000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:72591200-72598200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:72591400-72595200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:72591400-72596600	Weak transcription	Fetal Muscle Leg	muscle
8	chr9:72591600-72596400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:72591800-72592600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr9:72591800-72595400	Weak transcription	NHDF-Ad	bronchial
11	chr9:72591800-72596200	Weak transcription	Osteobl	bone
12	chr9:72592000-72593200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr9:72592200-72593200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr9:72592200-72594400	Weak transcription	NHLF	lung
15	chr9:72592200-72595600	Weak transcription	HSMM	muscle
16	chr9:72592200-72595800	Weak transcription	HSMMtube	muscle
17	chr9:72592200-72596200	Weak transcription	HMEC	breast
18	chr9:72592200-72596400	Weak transcription	HUVEC	blood vessel
19	chr9:72592200-72596600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr9:72592200-72596600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:72592200-72596600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links