Variant report

Variant	rs10123546
Chromosome Location	chr9:100481738-100481739
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:100477106..100478683-chr9:100480479..100483251,2	MCF-7	breast:
2	chr9:100480674..100483581-chr9:100484932..100487285,2	K562	blood:
3	chr9:100471241..100474154-chr9:100481493..100483041,2	K562	blood:

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs10119687	0.92[ASN][1000 genomes]
rs10512254	0.82[ASN][1000 genomes]
rs10983424	0.95[ASN][1000 genomes]
rs10983428	0.95[ASN][1000 genomes]
rs12347253	0.91[ASN][1000 genomes]
rs12350221	0.95[ASN][1000 genomes]
rs12350946	0.95[ASN][1000 genomes]
rs16923112	0.82[ASN][1000 genomes]
rs16923677	0.88[ASN][1000 genomes]
rs16923815	0.95[ASN][1000 genomes]
rs2297155	0.82[ASN][1000 genomes]
rs2297156	0.80[ASN][1000 genomes]
rs2297157	0.82[ASN][1000 genomes]
rs2297158	0.80[ASN][1000 genomes]
rs2297159	0.80[ASN][1000 genomes]
rs2297160	0.82[ASN][1000 genomes]
rs2401635	0.82[ASN][1000 genomes]
rs28376250	0.95[ASN][1000 genomes]
rs3176623	0.82[ASN][1000 genomes]
rs3176624	0.82[ASN][1000 genomes]
rs3176626	0.82[ASN][1000 genomes]
rs3176628	0.82[ASN][1000 genomes]
rs3176629	0.82[ASN][1000 genomes]
rs3176637	0.82[ASN][1000 genomes]
rs3176638	0.82[ASN][1000 genomes]
rs3176642	0.82[ASN][1000 genomes]
rs3176644	0.82[ASN][1000 genomes]
rs3176645	0.82[ASN][1000 genomes]
rs3176651	0.82[ASN][1000 genomes]
rs3176654	0.82[ASN][1000 genomes]
rs3176659	0.82[ASN][1000 genomes]
rs3176665	0.82[ASN][1000 genomes]
rs3176668	0.82[ASN][1000 genomes]
rs3176669	0.82[ASN][1000 genomes]
rs3176670	0.82[ASN][1000 genomes]
rs3176673	0.82[ASN][1000 genomes]
rs3176675	0.82[ASN][1000 genomes]
rs3176682	0.82[ASN][1000 genomes]
rs3176685	0.82[ASN][1000 genomes]
rs3176688	0.82[ASN][1000 genomes]
rs3176694	0.82[ASN][1000 genomes]
rs3176698	0.82[ASN][1000 genomes]
rs3176700	0.82[ASN][1000 genomes]
rs3176703	0.82[ASN][1000 genomes]
rs3176708	0.82[ASN][1000 genomes]
rs3176714	0.82[ASN][1000 genomes]
rs3176720	0.82[ASN][1000 genomes]
rs3176721	0.82[ASN][1000 genomes]
rs3176723	0.82[ASN][1000 genomes]
rs3176724	0.82[ASN][1000 genomes]
rs3176726	0.82[ASN][1000 genomes]
rs3176728	0.82[ASN][1000 genomes]
rs3176734	0.82[ASN][1000 genomes]
rs3176735	0.82[ASN][1000 genomes]
rs3176736	0.82[ASN][1000 genomes]
rs3176739	0.82[ASN][1000 genomes]
rs3176740	0.82[ASN][1000 genomes]
rs3176744	0.82[ASN][1000 genomes]
rs3176745	1.00[EUR][1000 genomes]
rs3176746	0.82[ASN][1000 genomes]
rs3176747	0.82[ASN][1000 genomes]
rs3176751	0.82[ASN][1000 genomes]
rs3176752	0.82[ASN][1000 genomes]
rs3176758	0.82[ASN][1000 genomes]
rs3176759	0.82[ASN][1000 genomes]
rs4480232	0.92[ASN][1000 genomes]
rs56052819	0.82[ASN][1000 genomes]
rs56200116	0.82[ASN][1000 genomes]
rs57598118	0.82[ASN][1000 genomes]
rs57612395	0.97[ASN][1000 genomes]
rs57940370	0.82[ASN][1000 genomes]
rs59205756	0.82[ASN][1000 genomes]
rs59354722	0.82[ASN][1000 genomes]
rs59775587	0.82[ASN][1000 genomes]
rs60463150	0.82[ASN][1000 genomes]
rs60821994	0.82[ASN][1000 genomes]
rs61047578	0.95[ASN][1000 genomes]
rs61208411	0.82[ASN][1000 genomes]
rs61440789	0.82[ASN][1000 genomes]
rs7033255	1.00[EUR][1000 genomes]
rs7045160	0.82[ASN][1000 genomes]
rs73498377	0.82[ASN][1000 genomes]
rs73498380	0.82[ASN][1000 genomes]
rs73498381	0.82[ASN][1000 genomes]
rs73498394	0.82[ASN][1000 genomes]
rs73500325	0.82[ASN][1000 genomes]
rs73500326	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73500328	0.82[ASN][1000 genomes]
rs73500393	0.82[ASN][1000 genomes]
rs73500395	0.82[ASN][1000 genomes]
rs73500396	0.82[ASN][1000 genomes]
rs73500397	0.82[ASN][1000 genomes]
rs73500398	0.82[ASN][1000 genomes]
rs73500400	0.82[ASN][1000 genomes]
rs73500402	1.00[EUR][1000 genomes]
rs73502204	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7850986	0.80[ASN][1000 genomes]
rs7862356	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]

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	nsv893610	chr9:100324086-100496160	Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv1043753	chr9:100458109-100599265	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100480400-100482600	Weak transcription	HSMMtube	muscle

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