Variant report

Variant	rs9883257
Chromosome Location	chr3:120651787-120651788
allele	C/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:42)

rs_ID	r²[population]
rs1523507	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1623244	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1683975	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1688683	0.92[EUR][1000 genomes]
rs1688684	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1795414	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2331521	0.92[EUR][1000 genomes]
rs2331527	0.90[EUR][1000 genomes]
rs2686651	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3108752	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34168323	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35345840	0.92[EUR][1000 genomes]
rs35645356	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3845849	0.90[EUR][1000 genomes]
rs3856575	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4510329	0.90[EUR][1000 genomes]
rs4630876	0.92[EUR][1000 genomes]
rs470502	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs470738	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs488416	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs571545	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs589682	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs590436	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs590663	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs603635	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs603847	0.87[EUR][1000 genomes]
rs619802	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs623175	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs638343	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs661160	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs662110	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs663363	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs680233	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6805670	0.90[EUR][1000 genomes]
rs6807604	0.87[EUR][1000 genomes]
rs682394	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs702008	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7615991	0.88[EUR][1000 genomes]
rs7616466	0.87[EUR][1000 genomes]
rs9844667	0.90[EUR][1000 genomes]
rs9866746	0.91[EUR][1000 genomes]
rs9872110	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007557	chr3:119892894-120764353	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv536706	chr3:119892894-120764353	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv869548	chr3:120320731-121076337	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv916869	chr3:120360281-120973169	Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv829700	chr3:120469191-120675763	Strong transcription Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:120645200-120658200	Weak transcription	Brain Angular Gyrus	brain
2	chr3:120646200-120661400	Weak transcription	Ovary	ovary
3	chr3:120648200-120654000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links