Variant report

Variant	rs1870783
Chromosome Location	chr18:39861568-39861569
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs1026595	1.00[ASN][1000 genomes]
rs1026596	1.00[ASN][1000 genomes]
rs10502780	0.92[ASN][1000 genomes]
rs11082268	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12455999	0.95[EUR][1000 genomes]
rs12457855	1.00[ASN][1000 genomes]
rs12457879	1.00[ASN][1000 genomes]
rs12457881	1.00[ASN][1000 genomes]
rs12605925	1.00[ASN][1000 genomes]
rs12956046	1.00[ASN][1000 genomes]
rs12962756	0.84[ASN][1000 genomes]
rs12967041	1.00[ASN][1000 genomes]
rs12967873	1.00[ASN][1000 genomes]
rs1381349	0.92[ASN][1000 genomes]
rs1461715	1.00[ASN][1000 genomes]
rs1461717	1.00[ASN][1000 genomes]
rs1461718	0.93[ASN][1000 genomes]
rs1461719	1.00[CEU][hapmap];0.93[YRI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1461721	0.92[ASN][1000 genomes]
rs1461723	0.91[EUR][1000 genomes]
rs1599478	0.87[EUR][1000 genomes]
rs1870781	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1870782	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1870785	1.00[ASN][1000 genomes]
rs2219638	0.92[ASN][1000 genomes]
rs2335779	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34703522	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35073620	0.92[ASN][1000 genomes]
rs35250842	0.86[ASN][1000 genomes]
rs35959504	0.92[ASN][1000 genomes]
rs4890391	1.00[ASN][1000 genomes]
rs4890393	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4890394	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4890395	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62082201	0.92[ASN][1000 genomes]
rs6507469	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7228003	0.88[EUR][1000 genomes]
rs7235905	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7236024	0.92[ASN][1000 genomes]
rs7238496	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7241462	1.00[ASN][1000 genomes]
rs8085350	1.00[ASN][1000 genomes]
rs8085753	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8089080	0.93[EUR][1000 genomes]
rs8089100	0.92[ASN][1000 genomes]
rs882289	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs882290	1.00[ASN][1000 genomes]
rs882291	1.00[ASN][1000 genomes]
rs898785	1.00[ASN][1000 genomes]
rs898786	1.00[ASN][1000 genomes]
rs898790	1.00[ASN][1000 genomes]
rs898791	1.00[ASN][1000 genomes]
rs898792	1.00[ASN][1000 genomes]
rs898793	1.00[ASN][1000 genomes]
rs898794	1.00[ASN][1000 genomes]
rs9304268	0.92[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	nsv949609	chr18:39126941-40070286	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	esv34153	chr18:39398768-39872265	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1059409	chr18:39711099-40139446	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1063343	chr18:39760943-39898498	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
5	nsv1059553	chr18:39828781-39872695	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39855200-39866000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr18:39860400-39862000	Enhancers	Fetal Intestine Small	intestine
3	chr18:39861200-39862400	Enhancers	Fetal Intestine Large	intestine

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