Variant report

Variant	rs7747261
Chromosome Location	chr6:75600908-75600909
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 134 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:123)

rs_ID	r²[population]
rs10080721	0.85[ASN][1000 genomes]
rs12661592	0.87[ASN][1000 genomes]
rs12662661	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12663829	0.98[ASN][1000 genomes]
rs12663977	0.85[ASN][1000 genomes]
rs12664010	0.85[ASN][1000 genomes]
rs12664096	0.87[ASN][1000 genomes]
rs12664513	0.87[ASN][1000 genomes]
rs12664807	0.89[ASN][1000 genomes]
rs12664984	0.89[ASN][1000 genomes]
rs12665297	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs12665702	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12665801	0.89[ASN][1000 genomes]
rs13437111	1.00[CEU][hapmap]
rs16885835	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.98[ASN][1000 genomes]
rs16885844	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs16885865	0.90[ASN][1000 genomes]
rs16885904	0.89[ASN][1000 genomes]
rs16885908	0.89[ASN][1000 genomes]
rs16885914	0.87[ASN][1000 genomes]
rs16885916	0.87[ASN][1000 genomes]
rs16885971	0.85[ASN][1000 genomes]
rs2353249	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2353251	0.87[ASN][1000 genomes]
rs2883118	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];0.88[ASN][1000 genomes]
rs28832995	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs35129971	0.89[ASN][1000 genomes]
rs35835665	0.89[ASN][1000 genomes]
rs35871031	0.89[ASN][1000 genomes]
rs4085727	0.89[ASN][1000 genomes]
rs4085729	0.90[ASN][1000 genomes]
rs4085730	0.90[ASN][1000 genomes]
rs4085731	0.89[ASN][1000 genomes]
rs4112825	0.90[ASN][1000 genomes]
rs4112826	0.90[ASN][1000 genomes]
rs4286732	0.80[AMR][1000 genomes]
rs4388259	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.94[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4495246	0.85[ASN][1000 genomes]
rs4612126	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs5023496	1.00[CEU][hapmap]
rs560250	1.00[CEU][hapmap]
rs57183891	0.89[ASN][1000 genomes]
rs57290574	0.89[ASN][1000 genomes]
rs57560334	0.89[ASN][1000 genomes]
rs57904603	0.82[ASN][1000 genomes]
rs581649	1.00[CEU][hapmap]
rs58699375	0.89[ASN][1000 genomes]
rs59041629	0.89[ASN][1000 genomes]
rs59051124	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59154474	0.89[ASN][1000 genomes]
rs59364413	0.99[AFR][1000 genomes]
rs59617477	0.85[ASN][1000 genomes]
rs59695593	0.85[ASN][1000 genomes]
rs59848727	0.89[ASN][1000 genomes]
rs60108944	0.89[ASN][1000 genomes]
rs60321049	0.85[ASN][1000 genomes]
rs60356008	0.89[ASN][1000 genomes]
rs60555684	0.85[ASN][1000 genomes]
rs60909334	0.85[ASN][1000 genomes]
rs61308045	0.85[ASN][1000 genomes]
rs61380374	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs61612838	0.89[ASN][1000 genomes]
rs6453790	0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6453795	0.91[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6453797	0.85[ASN][1000 genomes]
rs6453798	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6910855	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6916626	0.85[ASN][1000 genomes]
rs6917149	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6920790	0.81[AFR][1000 genomes]
rs6922193	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6923380	0.85[ASN][1000 genomes]
rs6929192	0.94[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6932000	1.00[CEU][hapmap];0.90[CHB][hapmap];0.96[CHD][hapmap];0.87[GIH][hapmap];0.86[MEX][hapmap];0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6932942	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6935326	0.91[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6940086	0.90[AFR][1000 genomes]
rs73458044	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs73458047	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7451287	0.85[ASN][1000 genomes]
rs7738809	1.00[CEU][hapmap]
rs7739660	0.85[ASN][1000 genomes]
rs7743883	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes]
rs7746348	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7749000	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7749133	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7753238	0.84[ASN][1000 genomes]
rs7754400	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs7755906	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.92[MKK][hapmap];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7769481	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7769487	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7772503	1.00[CEU][hapmap];0.90[CHB][hapmap];0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7772564	0.85[ASN][1000 genomes]
rs7775765	1.00[CEU][hapmap];0.90[CHB][hapmap];0.96[CHD][hapmap];0.87[GIH][hapmap];0.85[MEX][hapmap];0.85[ASN][1000 genomes]
rs7776027	1.00[CEU][hapmap];0.90[CHB][hapmap];0.85[ASN][1000 genomes]
rs9293988	1.00[CEU][hapmap]
rs9443092	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9443095	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9443096	0.98[ASN][1000 genomes]
rs9443100	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9443104	0.84[ASN][1000 genomes]
rs9443110	0.99[AFR][1000 genomes]
rs9443124	0.85[ASN][1000 genomes]
rs9443126	0.85[ASN][1000 genomes]
rs9443129	0.85[ASN][1000 genomes]
rs9447317	1.00[CEU][hapmap]
rs9447335	0.94[ASN][1000 genomes]
rs9447337	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9447339	0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9447343	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9447370	1.00[CEU][hapmap];0.90[CHB][hapmap];0.92[CHD][hapmap];0.92[JPT][hapmap];0.85[MEX][hapmap];0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9447371	0.89[ASN][1000 genomes]
rs9447374	0.89[ASN][1000 genomes]
rs9447376	0.89[ASN][1000 genomes]
rs9447377	0.89[ASN][1000 genomes]
rs9447378	0.87[ASN][1000 genomes]
rs9447379	0.87[ASN][1000 genomes]
rs9447380	0.87[ASN][1000 genomes]
rs9447386	0.85[ASN][1000 genomes]
rs9447388	0.85[ASN][1000 genomes]
rs9447391	0.85[ASN][1000 genomes]
rs9447394	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9447399	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520746	chr6:75211546-75691814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv917283	chr6:75234428-75641440	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv886169	chr6:75432861-75610722	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2757179	chr6:75525739-75625251	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv2759443	chr6:75525739-75625251	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv886173	chr6:75527856-75610722	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv886175	chr6:75536940-75610722	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv830696	chr6:75538316-75734609	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv886178	chr6:75539434-75610722	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv886180	chr6:75551717-75610722	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv1032153	chr6:75590017-75625051	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75589600-75601000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:75598800-75601000	Weak transcription	Ovary	ovary
3	chr6:75600400-75602000	Enhancers	NHLF	lung
4	chr6:75600800-75601000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:75600800-75601200	Flanking Active TSS	NHDF-Ad	bronchial
6	chr6:75600800-75601400	Enhancers	HSMMtube	muscle
7	chr6:75600800-75601600	Enhancers	Adipose Nuclei	Adipose
8	chr6:75600800-75601600	Enhancers	Fetal Muscle Leg	muscle
9	chr6:75600800-75601600	Enhancers	Fetal Stomach	stomach
10	chr6:75600800-75601800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr6:75600800-75602000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:75600800-75602000	Enhancers	Fetal Kidney	kidney
13	chr6:75600800-75602000	Enhancers	Rectal Smooth Muscle	rectum
14	chr6:75600800-75602200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:75600800-75602200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr6:75600800-75602200	Enhancers	Fetal Lung	lung
17	chr6:75600800-75602600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr6:75600800-75602800	Enhancers	Osteobl	bone

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