Variant report

Variant	rs17010457
Chromosome Location	chr1:221809272-221809273
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10082031	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10082119	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10449312	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10495171	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11118769	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11118771	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12058091	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12060691	0.94[AFR][1000 genomes]
rs12063275	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12063464	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12064012	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12064162	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12067974	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12075242	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12079769	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12081273	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12081326	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12082182	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12082815	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12082874	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12084065	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12086252	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12086291	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12088112	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12089796	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12092891	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12093053	1.00[CEU][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12094911	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12095828	1.00[CEU][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12095905	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13376358	0.88[EUR][1000 genomes]
rs17010395	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17010397	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17010409	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17010428	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17010434	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17010463	0.87[ASW][hapmap];1.00[CEU][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1890243	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1973728	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28515661	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56971545	1.00[EUR][1000 genomes]
rs57255089	1.00[EUR][1000 genomes]
rs58173559	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58482927	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59383649	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59680640	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59837278	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60152531	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60217573	1.00[EUR][1000 genomes]
rs61079406	1.00[EUR][1000 genomes]
rs61221236	0.90[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs73117552	0.88[EUR][1000 genomes]
rs74145360	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74145363	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74145364	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74145365	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74145366	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74145367	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74145373	0.94[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs74145375	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74145376	0.95[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs74145378	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74145394	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74145400	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9308402	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv873200	chr1:221644180-221843191	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1011037	chr1:221756526-221809552	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221806000-221811200	Weak transcription	Fetal Heart	heart
2	chr1:221806200-221813600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:221807000-221809400	Enhancers	K562	blood
4	chr1:221807600-221809400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr1:221808800-221809400	Enhancers	NHEK	skin
6	chr1:221809200-221811000	Weak transcription	HMEC	breast

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