Variant report

Variant	rs11120166
Chromosome Location	chr1:213770437-213770438
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	chr1:213753502..213756205-chr1:213769622..213772542,2	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs12021535	0.91[ASN][1000 genomes]
rs12023183	0.91[ASN][1000 genomes]
rs12024015	0.93[ASN][1000 genomes]
rs12024904	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12026459	0.91[ASN][1000 genomes]
rs12026491	0.91[ASN][1000 genomes]
rs12029072	0.85[ASN][1000 genomes]
rs12031624	0.93[ASN][1000 genomes]
rs12033788	0.91[ASN][1000 genomes]
rs12040529	0.85[ASN][1000 genomes]
rs12044623	0.85[ASN][1000 genomes]
rs12044697	0.85[ASN][1000 genomes]
rs12045032	0.85[ASN][1000 genomes]
rs12048306	0.89[ASN][1000 genomes]
rs12049107	0.93[ASN][1000 genomes]
rs12062055	1.00[ASN][1000 genomes]
rs12062324	1.00[ASN][1000 genomes]
rs12063434	1.00[ASN][1000 genomes]
rs12069418	0.92[AFR][1000 genomes]
rs12077007	0.92[AFR][1000 genomes]
rs12077375	1.00[ASN][1000 genomes]
rs12078742	1.00[ASN][1000 genomes]
rs12078860	1.00[ASN][1000 genomes]
rs17021041	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17021061	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs400857	1.00[JPT][hapmap]
rs412878	1.00[JPT][hapmap]
rs420627	1.00[JPT][hapmap]
rs436112	1.00[JPT][hapmap]
rs4394615	0.93[ASN][1000 genomes]
rs4475718	0.91[ASN][1000 genomes]
rs55816435	0.91[ASN][1000 genomes]
rs56254675	0.91[ASN][1000 genomes]
rs56352066	0.91[ASN][1000 genomes]
rs56714901	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58537941	0.93[ASN][1000 genomes]
rs60223676	1.00[ASN][1000 genomes]
rs61197031	1.00[ASN][1000 genomes]
rs61616602	0.93[ASN][1000 genomes]
rs6661042	1.00[ASN][1000 genomes]
rs67490848	0.82[ASN][1000 genomes]
rs72747785	0.85[ASN][1000 genomes]
rs72747794	0.85[ASN][1000 genomes]
rs72747798	0.85[ASN][1000 genomes]
rs72747801	0.85[ASN][1000 genomes]
rs72749621	0.95[ASN][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	nsv832525	chr1:213580476-213782815	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3345878	chr1:213714352-213841547	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3426755	chr1:213714443-213841514	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3378592	chr1:213714463-213841484	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr1:213769000-213775800	Weak transcription	HepG2	liver
2	chr1:213769600-213771000	Enhancers	Pancreas	Pancrea

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