Variant report

Variant	rs258118
Chromosome Location	chr5:58703713-58703714
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs165940	0.90[EUR][1000 genomes]
rs16889733	0.90[EUR][1000 genomes]
rs185417	0.94[ASN][1000 genomes]
rs187368	0.90[EUR][1000 genomes]
rs2441091	0.81[AMR][1000 genomes]
rs244582	0.81[AMR][1000 genomes]
rs244583	0.81[AMR][1000 genomes]
rs244590	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs244591	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs244592	0.90[EUR][1000 genomes]
rs244593	0.90[EUR][1000 genomes]
rs244594	0.88[EUR][1000 genomes]
rs244595	0.90[EUR][1000 genomes]
rs244596	0.90[EUR][1000 genomes]
rs244597	0.90[EUR][1000 genomes]
rs258112	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs258113	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs258114	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs258115	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs258116	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs258117	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs258122	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs258126	0.93[ASN][1000 genomes]
rs258127	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs258128	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2591750	0.89[ASN][1000 genomes]
rs365223	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs368538	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs370891	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs378858	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs380993	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs383046	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs387647	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs392901	0.91[ASN][1000 genomes]
rs403672	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs403695	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs424839	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs427433	0.90[EUR][1000 genomes]
rs428059	0.90[EUR][1000 genomes]
rs431645	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs432879	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs433161	0.90[EUR][1000 genomes]
rs434183	0.87[EUR][1000 genomes]
rs434274	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs434422	0.90[EUR][1000 genomes]
rs441817	0.90[EUR][1000 genomes]
rs444552	0.90[EUR][1000 genomes]
rs454702	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs530656	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs531511	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60448063	0.84[ASN][1000 genomes]
rs611540	0.81[EUR][1000 genomes]
rs611541	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023628	chr5:58557950-58757438	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv917274	chr5:58565291-58814374	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1030716	chr5:58636116-58718362	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv881705	chr5:58668669-58745872	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1028022	chr5:58673780-58786468	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1034656	chr5:58674724-58755580	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv598253	chr5:58675538-58754510	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58682000-58711800	Weak transcription	Psoas Muscle	Psoas
2	chr5:58697800-58703800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:58702400-58703800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr5:58702400-58704800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:58703000-58705600	ZNF genes & repeats	A549	lung
6	chr5:58703200-58704600	ZNF genes & repeats	Fetal Lung	lung
7	chr5:58703600-58704200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
8	chr5:58703600-58704400	ZNF genes & repeats	Fetal Intestine Large	intestine
9	chr5:58703600-58704600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
10	chr5:58703600-58704600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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