Variant report

Variant	rs55862662
Chromosome Location	chr4:147937413-147937414
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10519843	1.00[EUR][1000 genomes]
rs10519858	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1370302	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1437260	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022075	1.00[EUR][1000 genomes]
rs17022182	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022229	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022275	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022292	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28694531	1.00[EUR][1000 genomes]
rs4301138	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55789811	1.00[EUR][1000 genomes]
rs56919404	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59033491	1.00[EUR][1000 genomes]
rs6537442	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6811983	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6813219	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6840129	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6850704	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6851748	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6857268	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73852707	1.00[EUR][1000 genomes]
rs73852718	1.00[EUR][1000 genomes]
rs73852721	1.00[EUR][1000 genomes]
rs73852722	1.00[EUR][1000 genomes]
rs73852734	1.00[EUR][1000 genomes]
rs73852736	1.00[EUR][1000 genomes]
rs73852787	1.00[EUR][1000 genomes]
rs73852788	1.00[EUR][1000 genomes]
rs73852789	1.00[EUR][1000 genomes]
rs73852790	1.00[EUR][1000 genomes]
rs73852791	1.00[EUR][1000 genomes]
rs73852795	1.00[EUR][1000 genomes]
rs73852796	1.00[EUR][1000 genomes]
rs73852797	1.00[EUR][1000 genomes]
rs73853259	1.00[EUR][1000 genomes]
rs73853275	1.00[EUR][1000 genomes]
rs73853277	1.00[EUR][1000 genomes]
rs73853283	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73853285	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73853295	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73855102	1.00[EUR][1000 genomes]
rs73856354	1.00[AMR][1000 genomes];1.00[EUR][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	nsv880240	chr4:147905897-148032003	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv461676	chr4:147927227-147962432	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv595652	chr4:147927227-147962432	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv1016598	chr4:147931134-148012064	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147936800-147938000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr4:147936800-147940000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:147937200-147938200	Weak transcription	NHDF-Ad	bronchial
4	chr4:147937400-147937800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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