Variant report

Variant	rs13414172
Chromosome Location	chr2:187701561-187701562
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:187700922..187703123-chr2:187703577..187706331,2	K562	blood:
2	chr2:187697207..187699413-chr2:187700171..187702013,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10164815	1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[TSI][hapmap];0.99[EUR][1000 genomes]
rs10172225	0.91[CEU][hapmap];0.83[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs10175178	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs10178860	0.96[EUR][1000 genomes]
rs10179175	0.96[EUR][1000 genomes]
rs10181270	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs10188450	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs10188850	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs10188869	0.89[CEU][hapmap];0.99[EUR][1000 genomes]
rs10189037	0.83[CEU][hapmap];0.88[GIH][hapmap];0.90[TSI][hapmap];0.99[EUR][1000 genomes]
rs10191094	0.96[EUR][1000 genomes]
rs10191209	0.96[EUR][1000 genomes]
rs10195632	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs10195758	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs10202588	1.00[CEU][hapmap]
rs10204903	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs11894819	0.93[EUR][1000 genomes]
rs11898022	0.93[EUR][1000 genomes]
rs11898112	0.96[EUR][1000 genomes]
rs11898665	0.99[EUR][1000 genomes]
rs11898741	0.99[EUR][1000 genomes]
rs13399866	0.99[EUR][1000 genomes]
rs13400804	1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[TSI][hapmap];0.99[EUR][1000 genomes]
rs13401173	0.96[EUR][1000 genomes]
rs13401579	0.96[EUR][1000 genomes]
rs13404398	0.96[EUR][1000 genomes]
rs13407627	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13414169	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs13426438	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs17852915	0.96[EUR][1000 genomes]
rs17852916	0.96[EUR][1000 genomes]
rs17856918	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs35121986	0.96[EUR][1000 genomes]
rs4429438	0.93[EUR][1000 genomes]
rs4545967	0.93[EUR][1000 genomes]
rs62171870	0.93[EUR][1000 genomes]
rs62171891	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6434197	1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[TSI][hapmap];0.99[EUR][1000 genomes]
rs6708289	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs6711860	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs6722473	0.96[EUR][1000 genomes]
rs6722495	0.93[EUR][1000 genomes]
rs6733279	0.96[EUR][1000 genomes]
rs6736846	0.93[EUR][1000 genomes]
rs6744956	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6745065	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6745572	1.00[CEU][hapmap];0.83[GIH][hapmap];0.96[EUR][1000 genomes]
rs6745642	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6750961	0.96[EUR][1000 genomes]
rs6751106	0.91[EUR][1000 genomes]
rs6751828	0.96[EUR][1000 genomes]
rs6752200	0.96[EUR][1000 genomes]
rs6760362	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs7595459	0.93[EUR][1000 genomes]
rs7598838	0.93[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428069	chr2:187575692-187766209	ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	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	chr2:187700400-187701600	Enhancers	Osteobl	bone
2	chr2:187701000-187706800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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