Variant report

Variant	rs2817864
Chromosome Location	chr1:71503105-71503106
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:71499543..71503702-chr1:71511179..71513554,5	K562	blood:

Variant related genes	Relation type
ENSG00000050628	Chromatin interaction

Extended variants
information (count: 86 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs1022527	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1022529	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10399632	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10399704	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10399705	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10399706	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10399797	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10399806	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10493481	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10749799	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10789315	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10789316	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11209731	0.86[ASN][1000 genomes]
rs11209733	0.88[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.89[JPT][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11209736	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11209739	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11209740	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11209743	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11209747	0.81[EUR][1000 genomes]
rs12120041	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12130153	0.88[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.89[JPT][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12134962	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12139719	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12139935	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12739047	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12739685	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12748649	0.81[EUR][1000 genomes]
rs12756951	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12757161	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1983588	0.88[CHB][hapmap];0.93[CHD][hapmap];0.89[JPT][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.87[ASN][1000 genomes]
rs1988080	0.80[AMR][1000 genomes]
rs2143157	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2179412	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2206345	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2206346	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2223502	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2268054	0.87[ASN][1000 genomes]
rs2268055	0.88[CHB][hapmap];0.93[CHD][hapmap];0.89[JPT][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap];0.87[ASN][1000 genomes]
rs2268056	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2268058	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2268059	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2268060	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2268061	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2268062	0.94[CHB][hapmap];0.97[CHD][hapmap];0.83[JPT][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap];0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2300166	0.89[JPT][hapmap]
rs2300167	0.83[CHD][hapmap];0.89[JPT][hapmap];0.84[MEX][hapmap]
rs2300169	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2300170	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2300171	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2300173	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2300175	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2300178	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2796203	0.83[JPT][hapmap]
rs2817865	0.87[ASN][1000 genomes]
rs2817866	0.87[ASN][1000 genomes]
rs2901523	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs33936437	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs3765892	0.94[CHB][hapmap];0.89[JPT][hapmap];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs3765894	0.94[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.89[JPT][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4128461	0.98[TSI][hapmap];0.83[EUR][1000 genomes]
rs4272572	0.80[CHD][hapmap]
rs4361943	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4425937	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4437828	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4439319	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4511057	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4520371	0.98[TSI][hapmap];0.83[EUR][1000 genomes]
rs4549988	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4650099	0.81[EUR][1000 genomes]
rs4650100	0.82[EUR][1000 genomes]
rs5680	0.83[CHB][hapmap];0.83[JPT][hapmap]
rs5682	0.88[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.89[JPT][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6679370	0.89[JPT][hapmap]
rs7525785	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7556650	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8179367	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8179390	0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8179408	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs880098	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs997997	0.94[CHB][hapmap];0.97[CHD][hapmap];0.80[GIH][hapmap];0.89[JPT][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap];0.85[AMR][1000 genomes];0.87[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	esv1845198	chr1:71274759-71514969	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv546472	chr1:71432984-71541003	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	555 gene(s)	inside rSNPs	diseases
3	nsv461851	chr1:71442626-71507541	Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
4	nsv546473	chr1:71442626-71507541	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
5	esv1850593	chr1:71444149-71514969	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv871242	chr1:71481050-71519326	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2817864	PTGER3	cis	uninvolved skin	skin_eQTL
rs2817864	PTGER3	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71492800-71504400	Weak transcription	Gastric	stomach
2	chr1:71496000-71506200	Weak transcription	Fetal Stomach	stomach
3	chr1:71497600-71510600	Weak transcription	Aorta	Aorta
4	chr1:71499000-71505800	Weak transcription	NHDF-Ad	bronchial
5	chr1:71501200-71503200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:71502600-71503200	Strong transcription	Adipose Nuclei	Adipose
7	chr1:71502600-71503600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:71502800-71503600	Enhancers	Rectal Smooth Muscle	rectum
9	chr1:71503000-71505000	Genic enhancers	K562	blood
10	chr1:71503000-71511200	Weak transcription	Pancreas	Pancrea

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