Variant report

Variant	rs1860855
Chromosome Location	chr7:122278639-122278640
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs12530951	0.92[JPT][hapmap]
rs12533063	0.93[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12538945	0.98[ASN][1000 genomes]
rs1476898	0.93[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1544594	0.93[JPT][hapmap]
rs1544595	0.93[JPT][hapmap]
rs1860857	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2109968	0.93[JPT][hapmap]
rs2159827	0.92[JPT][hapmap]
rs2192017	0.84[JPT][hapmap]
rs2192018	0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2215665	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2215668	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2251761	0.92[JPT][hapmap]
rs2402618	0.82[ASN][1000 genomes]
rs2430016	0.93[JPT][hapmap];0.80[ASN][1000 genomes]
rs2430018	0.82[ASN][1000 genomes]
rs2430020	0.88[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2430021	0.84[ASN][1000 genomes]
rs2430022	0.92[JPT][hapmap];0.82[ASN][1000 genomes]
rs2430023	0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2430030	0.92[JPT][hapmap]
rs2430031	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs2430042	0.93[JPT][hapmap]
rs2430044	0.91[JPT][hapmap];0.96[YRI][hapmap]
rs2430045	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2430047	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2430048	0.82[AFR][1000 genomes]
rs2430049	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2430053	0.93[JPT][hapmap];0.84[ASN][1000 genomes]
rs2471189	0.92[JPT][hapmap]
rs2471190	0.93[JPT][hapmap]
rs2471191	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2471193	0.82[CHB][hapmap];0.92[JPT][hapmap]
rs2471194	0.93[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs2471195	0.92[JPT][hapmap]
rs2471196	0.92[JPT][hapmap]
rs2471199	0.92[JPT][hapmap];1.00[YRI][hapmap];0.82[ASN][1000 genomes]
rs2471200	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2471202	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2471203	0.82[ASN][1000 genomes]
rs2471204	0.80[ASN][1000 genomes]
rs2471206	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2471207	0.80[ASN][1000 genomes]
rs2471211	0.84[ASN][1000 genomes]
rs2471212	0.93[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2471215	0.93[EUR][1000 genomes]
rs2471216	0.93[EUR][1000 genomes]
rs4285412	0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs67776758	0.98[ASN][1000 genomes]
rs7793961	0.93[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7797968	0.93[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017029	chr7:121958574-122338623	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv532178	chr7:122203056-122978846	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv532179	chr7:122249639-122986259	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 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	chr7:122269800-122288000	Weak transcription	HepG2	liver
2	chr7:122276400-122283400	Weak transcription	Fetal Lung	lung
3	chr7:122276800-122283200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr7:122278000-122279000	Enhancers	Esophagus	oesophagus
5	chr7:122278600-122279000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:122278600-122280200	Weak transcription	Lung	lung
7	chr7:122278600-122288200	Weak transcription	Gastric	stomach

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