Variant report

Variant	rs57963116
Chromosome Location	chr1:192721119-192721120
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:192720713..192722300-chr1:192723780..192725507,2	K562	blood:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10489515	1.00[EUR][1000 genomes]
rs10489517	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10921269	1.00[EUR][1000 genomes]
rs12091442	1.00[EUR][1000 genomes]
rs12093765	1.00[EUR][1000 genomes]
rs12096309	1.00[EUR][1000 genomes]
rs1342808	1.00[EUR][1000 genomes]
rs1418719	1.00[EUR][1000 genomes]
rs16834594	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16834597	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16834625	1.00[EUR][1000 genomes]
rs16834852	1.00[EUR][1000 genomes]
rs16834867	1.00[EUR][1000 genomes]
rs16834872	1.00[EUR][1000 genomes]
rs16834876	1.00[EUR][1000 genomes]
rs41512544	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs55747130	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56006394	1.00[AMR][1000 genomes]
rs56031935	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57149196	1.00[EUR][1000 genomes]
rs57189481	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57630083	1.00[EUR][1000 genomes]
rs57777171	0.89[AFR][1000 genomes]
rs57826402	1.00[EUR][1000 genomes]
rs57890252	1.00[EUR][1000 genomes]
rs60892638	1.00[EUR][1000 genomes]
rs61030187	1.00[AMR][1000 genomes]
rs6680350	1.00[EUR][1000 genomes]
rs6683145	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6689962	1.00[EUR][1000 genomes]
rs6702235	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6702236	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73060168	1.00[EUR][1000 genomes]
rs73060190	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73062239	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73062264	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73062267	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73062271	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73062273	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73062285	1.00[EUR][1000 genomes]
rs73062286	1.00[EUR][1000 genomes]
rs73062290	1.00[EUR][1000 genomes]
rs73064112	1.00[EUR][1000 genomes]
rs73064182	1.00[EUR][1000 genomes]
rs73064200	1.00[EUR][1000 genomes]
rs73066132	1.00[EUR][1000 genomes]
rs73068111	1.00[EUR][1000 genomes]
rs73068113	1.00[EUR][1000 genomes]
rs73068116	1.00[EUR][1000 genomes]
rs74130451	1.00[EUR][1000 genomes]
rs74130466	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7538953	1.00[EUR][1000 genomes]
rs7552270	1.00[EUR][1000 genomes]
rs7555263	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532618	chr1:192537006-193149179	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv548660	chr1:192609268-192945348	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
3	nsv997662	chr1:192715815-192740227	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:192720600-192723200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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