Variant report

Variant	rs10478464
Chromosome Location	chr5:119778450-119778451
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10036322	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10447269	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1108712	0.80[AMR][1000 genomes]
rs12109029	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13171950	0.83[EUR][1000 genomes]
rs13357775	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13359009	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13435941	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1347070	1.00[CEU][hapmap];0.83[YRI][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1368182	0.81[CEU][hapmap]
rs1368189	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1394115	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1432457	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1432461	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1432464	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1835870	1.00[ASN][1000 genomes]
rs2082353	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2082356	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2099297	0.87[AFR][1000 genomes]
rs2116606	0.82[AMR][1000 genomes]
rs35399227	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4895246	0.80[AMR][1000 genomes]
rs4895250	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4895253	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59264625	0.80[AMR][1000 genomes]
rs59336675	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6595232	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6865215	1.00[CEU][hapmap];0.81[YRI][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6878266	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6895493	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7446731	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs753641	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7701804	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7708836	0.82[AFR][1000 genomes]
rs7709140	1.00[ASN][1000 genomes]
rs7718509	0.81[AMR][1000 genomes]
rs7722765	1.00[ASN][1000 genomes]
rs7727978	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9327141	0.81[AMR][1000 genomes]
rs9327142	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs982827	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][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	nsv532200	chr5:119317901-120102513	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1018955	chr5:119679918-119802014	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1020655	chr5:119729801-119781762	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1018100	chr5:119749898-119802014	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119769200-119780800	Weak transcription	HSMM	muscle
2	chr5:119773200-119781000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:119777400-119784000	Enhancers	Fetal Heart	heart
4	chr5:119777800-119785200	Weak transcription	Psoas Muscle	Psoas

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