Variant report

Variant	rs9905226
Chromosome Location	chr17:63229475-63229476
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	chr17:63222163..63226262-chr17:63226769..63229619,4	MCF-7	breast:
2	chr17:63223609..63225528-chr17:63228836..63231724,2	K562	blood:

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs11079561	1.00[ASN][1000 genomes]
rs11654243	0.83[CEU][hapmap]
rs11658673	0.89[CEU][hapmap]
rs11658773	0.89[CEU][hapmap]
rs16960903	0.83[CEU][hapmap]
rs16960905	0.84[CEU][hapmap]
rs16960920	0.84[CEU][hapmap]
rs16960957	0.89[CEU][hapmap]
rs16961703	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16961727	1.00[ASN][1000 genomes]
rs16961732	1.00[ASN][1000 genomes]
rs16961868	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16961878	1.00[ASN][1000 genomes]
rs16961897	1.00[ASN][1000 genomes]
rs17689671	1.00[ASN][1000 genomes]
rs28476544	1.00[ASN][1000 genomes]
rs2869578	0.81[CEU][hapmap]
rs28895913	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4293415	0.84[CEU][hapmap]
rs4791220	0.94[CEU][hapmap]
rs4791223	0.83[CEU][hapmap]
rs4791227	0.83[CEU][hapmap]
rs55820790	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55853855	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55864812	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56202104	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56205487	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56408543	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56684368	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57333496	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58012124	1.00[ASN][1000 genomes]
rs58931966	0.82[EUR][1000 genomes]
rs60495439	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60919543	1.00[ASN][1000 genomes]
rs62063085	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62063086	1.00[ASN][1000 genomes]
rs62065142	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62065143	1.00[ASN][1000 genomes]
rs62065144	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62065147	1.00[ASN][1000 genomes]
rs6504287	0.86[EUR][1000 genomes]
rs6504288	0.84[EUR][1000 genomes]
rs67111745	1.00[ASN][1000 genomes]
rs7207480	1.00[ASN][1000 genomes]
rs7207726	0.88[CEU][hapmap]
rs7207744	1.00[ASN][1000 genomes]
rs7211786	1.00[ASN][1000 genomes]
rs7212442	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7213152	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7215623	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7219197	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7219498	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7219691	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7220948	1.00[ASN][1000 genomes]
rs7221051	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7221258	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7221276	1.00[ASN][1000 genomes]
rs7221428	1.00[ASN][1000 genomes]
rs7221810	1.00[ASN][1000 genomes]
rs72845315	0.86[ASN][1000 genomes]
rs72854623	0.86[ASN][1000 genomes]
rs7342966	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8065208	1.00[ASN][1000 genomes]
rs8071511	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8072237	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8074052	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8077032	1.00[ASN][1000 genomes]
rs8077396	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8078209	1.00[ASN][1000 genomes]
rs8078293	0.94[CEU][hapmap]
rs8078535	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8078847	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8080929	0.94[CEU][hapmap]
rs8081224	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8082275	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8082401	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs908089	0.84[CEU][hapmap]
rs9889653	0.89[CEU][hapmap]
rs9896245	0.83[CEU][hapmap]
rs9896491	0.84[EUR][1000 genomes]
rs9897086	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9897299	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9897592	0.81[CEU][hapmap]
rs9898094	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9905007	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9909786	1.00[CHB][hapmap]
rs9914176	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9916525	1.00[CEU][hapmap]

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	nsv530764	chr17:62939944-63278472	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv482610	chr17:63214370-63372334	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:63225400-63231600	Weak transcription	Osteobl	bone
2	chr17:63228400-63230600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr17:63228400-63232400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr17:63229400-63229800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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