Variant report

Variant	rs7645408
Chromosome Location	chr3:89446132-89446133
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1512185	0.82[ASN][1000 genomes]
rs17801001	0.94[CEU][hapmap];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17801031	0.94[CEU][hapmap];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28623022	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57670516	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62275015	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62275016	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62275018	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62275019	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6782527	0.94[CEU][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6800041	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73137381	0.83[ASN][1000 genomes]
rs73137382	0.83[ASN][1000 genomes]
rs73137384	0.86[ASN][1000 genomes]
rs73137387	0.83[ASN][1000 genomes]
rs73137393	0.83[ASN][1000 genomes]
rs73137395	0.86[ASN][1000 genomes]
rs7615949	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7631682	0.89[CEU][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs870898	0.94[CEU][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs870899	0.94[CEU][hapmap];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9832305	0.89[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9836340	0.88[CEU][hapmap];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9842599	0.88[CEU][hapmap];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9844971	0.83[CEU][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9849029	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9854073	0.94[CEU][hapmap];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9860266	0.89[CEU][hapmap];0.84[ASN][1000 genomes]
rs9864984	0.95[CEU][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9868782	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv437866	chr3:89247881-89480265	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1000694	chr3:89373820-89453045	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1008018	chr3:89382031-90254063	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv536639	chr3:89382031-90254063	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1002605	chr3:89413038-89453045	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1010932	chr3:89424428-90192503	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr3:89436600-89461800	Weak transcription	Fetal Brain Female	brain
2	chr3:89444200-89446400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:89445200-89447000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:89445400-89448400	Weak transcription	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links