Variant report

Variant	rs2610874
Chromosome Location	chr10:55769992-55769993
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

rs_ID	r²[population]
rs10740557	0.88[CEU][hapmap]
rs10740558	0.88[CEU][hapmap]
rs10763016	0.81[CEU][hapmap]
rs10763020	0.87[CEU][hapmap]
rs10763021	0.88[CEU][hapmap]
rs10763022	0.87[CEU][hapmap]
rs10763024	0.88[CEU][hapmap]
rs10763025	0.88[CEU][hapmap]
rs10763027	0.88[CEU][hapmap]
rs10825138	0.88[CEU][hapmap]
rs10825156	0.88[CEU][hapmap]
rs10825157	0.88[CEU][hapmap]
rs10825185	0.84[CEU][hapmap]
rs11003893	0.88[CEU][hapmap]
rs11003918	0.87[CEU][hapmap]
rs11003919	0.88[CEU][hapmap]
rs11003969	0.83[CEU][hapmap]
rs1900421	0.84[CEU][hapmap]
rs1900423	0.88[CEU][hapmap]
rs1900444	0.83[CEU][hapmap]
rs1900450	0.88[CEU][hapmap]
rs1900451	0.88[CEU][hapmap]
rs1900453	0.88[CEU][hapmap]
rs1900458	0.84[CEU][hapmap]
rs1900459	0.83[CEU][hapmap]
rs1911420	0.84[CEU][hapmap]
rs1911428	0.94[EUR][1000 genomes]
rs2121525	0.84[CEU][hapmap]
rs2135718	0.83[CEU][hapmap]
rs2135723	0.88[CEU][hapmap];0.90[EUR][1000 genomes]
rs2174716	0.88[CEU][hapmap]
rs2384328	0.88[CEU][hapmap]
rs2384340	0.88[CEU][hapmap]
rs2384343	0.84[CEU][hapmap]
rs2446599	0.82[EUR][1000 genomes]
rs2446600	0.92[CEU][hapmap]
rs2446608	0.81[CEU][hapmap]
rs2456699	0.81[CEU][hapmap]
rs2593103	0.88[CEU][hapmap]
rs2593105	0.88[CEU][hapmap]
rs2593106	0.88[CEU][hapmap]
rs2593120	0.88[CEU][hapmap]
rs2593122	0.88[CEU][hapmap]
rs2593123	0.88[CEU][hapmap]
rs2593129	0.87[CEU][hapmap]
rs2610823	0.88[CEU][hapmap]
rs2610837	0.84[CEU][hapmap]
rs2610893	0.80[CEU][hapmap]
rs2610902	0.85[CEU][hapmap]
rs2610909	0.81[CEU][hapmap]
rs2610910	0.81[CEU][hapmap]
rs2610912	0.88[CEU][hapmap]
rs2610919	0.88[CEU][hapmap]
rs2660178	0.92[CEU][hapmap];0.95[GIH][hapmap];0.86[MEX][hapmap];0.97[TSI][hapmap];0.95[EUR][1000 genomes]
rs2660197	0.81[CEU][hapmap]
rs2921912	0.88[CEU][hapmap]
rs2921924	0.88[CEU][hapmap]
rs2921925	0.88[CEU][hapmap]
rs2921926	0.88[CEU][hapmap]
rs2926391	0.88[CEU][hapmap]
rs2926397	0.88[CEU][hapmap]
rs2926404	0.92[CEU][hapmap]
rs2926410	0.84[CEU][hapmap]
rs4935485	0.88[CEU][hapmap]
rs4935487	0.84[CEU][hapmap]
rs5003374	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs6481043	0.87[CEU][hapmap]
rs6481045	0.84[CEU][hapmap]
rs7069577	0.88[CEU][hapmap]
rs7070828	0.91[CEU][hapmap]
rs7095839	0.88[CEU][hapmap]
rs7476991	0.81[CEU][hapmap]
rs7893789	0.88[CEU][hapmap]
rs7904289	0.88[CEU][hapmap]
rs7910658	0.88[CEU][hapmap]
rs7920872	0.88[CEU][hapmap]

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949692	chr10:55502542-55893206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv869303	chr10:55714219-55857931	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55769400-55770800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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