Variant report

Variant	rs1868715
Chromosome Location	chr4:121747970-121747971
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:121745652..121748462-chr4:121750150..121752192,2	MCF-7	breast:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10026047	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10033707	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10857072	1.00[CEU][hapmap];0.85[JPT][hapmap];0.82[MEX][hapmap];0.95[TSI][hapmap];0.89[EUR][1000 genomes]
rs11098589	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12509870	0.82[CEU][hapmap]
rs12509993	0.81[CEU][hapmap]
rs1349347	0.94[CEU][hapmap];0.81[CHB][hapmap];0.86[JPT][hapmap];0.86[MEX][hapmap];0.89[TSI][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1376099	0.94[CEU][hapmap];0.81[CHB][hapmap];0.86[JPT][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1397770	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1450462	0.84[CEU][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1511309	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1588523	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs17051263	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1877214	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1877215	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1912720	0.94[CEU][hapmap];0.80[CHB][hapmap];0.86[JPT][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1987468	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2100237	0.94[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.86[MEX][hapmap];0.89[TSI][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2122510	0.80[YRI][hapmap]
rs2136997	0.94[CEU][hapmap];0.80[CHB][hapmap];0.85[JPT][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs237212	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2597536	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2597537	0.94[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2597538	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2597540	0.94[CEU][hapmap];0.86[JPT][hapmap];0.86[MEX][hapmap];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2667172	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2667173	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28831670	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs343181	0.94[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.86[MEX][hapmap];0.89[TSI][hapmap];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs343184	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs343187	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs343190	0.94[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.82[MEX][hapmap];0.86[TSI][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs343192	0.94[CEU][hapmap];0.91[CHB][hapmap];0.97[CHD][hapmap];0.91[JPT][hapmap];0.91[MEX][hapmap];0.89[TSI][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3789141	0.93[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.88[TSI][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3789142	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3804174	0.86[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4833183	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4833184	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4833675	0.94[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4833676	0.94[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.86[MEX][hapmap];0.89[TSI][hapmap];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4833677	0.94[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4833679	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4833681	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57841364	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59085467	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59837089	0.81[EUR][1000 genomes]
rs6534216	0.94[ASW][hapmap];0.83[CEU][hapmap];0.80[YRI][hapmap]
rs6811794	0.83[ASW][hapmap]
rs6835471	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][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	nsv879852	chr4:121108734-121768496	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv998094	chr4:121504565-122374203	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv916737	chr4:121589793-121748847	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv461634	chr4:121623057-121765527	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv595334	chr4:121623057-121765527	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1013704	chr4:121657648-121791601	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121729600-121770400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr4:121730200-121753400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:121730400-121760000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:121730400-121760800	Weak transcription	Pancreas	Pancrea
5	chr4:121731200-121752400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:121732200-121754800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr4:121737400-121751400	Weak transcription	Psoas Muscle	Psoas
8	chr4:121737600-121759800	Weak transcription	Lung	lung
9	chr4:121737800-121754400	Weak transcription	Aorta	Aorta
10	chr4:121738200-121759600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr4:121738800-121750600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:121743600-121750000	Weak transcription	Fetal Heart	heart
13	chr4:121743800-121765400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr4:121745200-121751400	Weak transcription	Left Ventricle	heart
15	chr4:121746200-121748000	Enhancers	Fetal Intestine Small	intestine
16	chr4:121746600-121748000	Enhancers	Ovary	ovary
17	chr4:121746800-121748400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr4:121747200-121755400	Weak transcription	Fetal Intestine Large	intestine
19	chr4:121747600-121748000	Enhancers	Fetal Lung	lung
20	chr4:121747800-121748000	Enhancers	Pancreatic Islets	Pancreatic Islet

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