Variant report

Variant	rs17029108
Chromosome Location	chr4:100459346-100459347
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:100452738..100454334-chr4:100458012..100459573,2	K562	blood:
2	chr4:100458736..100461686-chr4:100868132..100870522,2	K562	blood:
3	chr4:100459336..100463167-chr4:100464703..100466787,3	K562	blood:
4	chr4:100457175..100460170-chr4:100461778..100463584,2	K562	blood:

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10000018	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10007794	0.89[EUR][1000 genomes]
rs10008896	0.90[EUR][1000 genomes]
rs10008928	0.90[EUR][1000 genomes]
rs10009198	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10019266	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10020461	0.88[EUR][1000 genomes]
rs10026790	0.86[EUR][1000 genomes]
rs10030937	0.90[EUR][1000 genomes]
rs10031512	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10516443	0.90[EUR][1000 genomes]
rs10516444	0.88[EUR][1000 genomes]
rs1054730	0.90[EUR][1000 genomes]
rs1057615	0.86[EUR][1000 genomes]
rs11933250	0.86[EUR][1000 genomes]
rs11933520	0.85[EUR][1000 genomes]
rs11933937	0.86[EUR][1000 genomes]
rs11935581	0.88[EUR][1000 genomes]
rs11937107	0.86[EUR][1000 genomes]
rs11937273	0.86[EUR][1000 genomes]
rs11941470	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11943031	0.86[EUR][1000 genomes]
rs11944752	0.86[EUR][1000 genomes]
rs11946292	0.89[EUR][1000 genomes]
rs11946367	0.90[EUR][1000 genomes]
rs11946658	0.86[EUR][1000 genomes]
rs11947558	0.85[EUR][1000 genomes]
rs1491235	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1503774	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1503778	0.86[EUR][1000 genomes]
rs17598226	0.86[EUR][1000 genomes]
rs1800591	0.86[EUR][1000 genomes]
rs1800803	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1800804	0.86[EUR][1000 genomes]
rs1873516	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1873517	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2089079	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28368786	0.86[EUR][1000 genomes]
rs28376611	0.86[EUR][1000 genomes]
rs28431971	0.84[EUR][1000 genomes]
rs28435607	0.86[EUR][1000 genomes]
rs28444681	0.89[EUR][1000 genomes]
rs28473262	0.86[EUR][1000 genomes]
rs28497720	0.86[EUR][1000 genomes]
rs28500697	0.89[EUR][1000 genomes]
rs28595160	0.86[EUR][1000 genomes]
rs28608631	0.89[EUR][1000 genomes]
rs28621060	0.89[EUR][1000 genomes]
rs28647519	0.86[EUR][1000 genomes]
rs2866164	0.86[EUR][1000 genomes]
rs28666735	0.86[EUR][1000 genomes]
rs28678377	0.85[EUR][1000 genomes]
rs28704064	0.86[EUR][1000 genomes]
rs28789770	0.86[EUR][1000 genomes]
rs28849180	0.86[EUR][1000 genomes]
rs2903201	0.90[EUR][1000 genomes]
rs3811800	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3816873	0.86[EUR][1000 genomes]
rs4423880	0.90[EUR][1000 genomes]
rs6532820	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6815231	0.90[EUR][1000 genomes]
rs6839296	0.86[EUR][1000 genomes]
rs6841211	0.86[EUR][1000 genomes]
rs72681967	0.89[EUR][1000 genomes]
rs7656665	0.86[EUR][1000 genomes]
rs7661453	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7661656	0.90[EUR][1000 genomes]
rs7661665	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7661964	0.85[EUR][1000 genomes]
rs7682548	0.85[EUR][1000 genomes]
rs7686425	0.90[EUR][1000 genomes]
rs7687762	0.86[EUR][1000 genomes]
rs7693203	0.86[EUR][1000 genomes]
rs7693979	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs867380	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs867381	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs884274	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs884275	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9307240	0.86[EUR][1000 genomes]
rs9990558	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9997840	0.88[EUR][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	nsv879656	chr4:99976646-100533722	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv3584519	chr4:100323870-100477462	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3584522	chr4:100432841-100467011	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv3584523	chr4:100437553-100476549	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100457200-100460600	Enhancers	Fetal Intestine Small	intestine
2	chr4:100457200-100462200	Enhancers	Fetal Intestine Large	intestine
3	chr4:100457600-100459600	Enhancers	Duodenum Mucosa	Duodenum
4	chr4:100457800-100459400	Enhancers	Liver	Liver
5	chr4:100458600-100484000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:100459000-100459400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:100459200-100461800	Weak transcription	Small Intestine	intestine

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