Variant report

Variant	rs10243981
Chromosome Location	chr7:3606338-3606339
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 149 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs10215541	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10215554	0.90[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.85[YRI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10215632	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10216009	0.90[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.85[YRI][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10227151	0.90[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10236989	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10238783	0.85[JPT][hapmap]
rs10241070	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10263702	0.80[JPT][hapmap];0.83[ASN][1000 genomes]
rs10264275	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10272876	0.90[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10277776	0.83[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs10499336	0.85[CEU][hapmap]
rs10499337	0.85[CEU][hapmap]
rs1114778	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1114779	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1114780	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11531491	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11531493	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12111969	0.89[CEU][hapmap];0.89[CHB][hapmap];0.88[JPT][hapmap];0.89[YRI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12670592	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12672248	0.90[CEU][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1403160	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1403161	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1522505	0.90[CEU][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1608136	0.90[CEU][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16870870	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs16870900	0.86[JPT][hapmap]
rs17133420	0.85[CEU][hapmap];0.90[JPT][hapmap];0.83[AMR][1000 genomes]
rs17133426	0.90[CEU][hapmap];0.90[JPT][hapmap];0.88[AMR][1000 genomes]
rs17133432	0.80[CEU][hapmap];0.80[CHB][hapmap];0.90[JPT][hapmap];0.88[AMR][1000 genomes]
rs17133439	0.80[CEU][hapmap];0.89[AMR][1000 genomes]
rs17133445	0.89[AMR][1000 genomes]
rs17133497	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17133501	0.90[CEU][hapmap];0.85[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17133520	0.84[CEU][hapmap];0.80[CHB][hapmap];0.90[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17133523	0.89[CEU][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17133529	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17133533	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17133535	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17133554	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17133555	0.90[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[AFR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17133566	0.83[CHB][hapmap];0.90[JPT][hapmap];0.94[ASN][1000 genomes]
rs17133591	0.86[JPT][hapmap]
rs1882427	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1882428	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1882429	0.89[CEU][hapmap];0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1922017	0.90[CEU][hapmap];0.90[JPT][hapmap];0.85[YRI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1922019	0.90[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2141819	0.85[JPT][hapmap]
rs2141821	0.85[JPT][hapmap]
rs2141825	0.93[ASN][1000 genomes]
rs2177168	0.85[CEU][hapmap];0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2178626	0.83[CHB][hapmap];0.95[JPT][hapmap];0.85[YRI][hapmap];0.93[ASN][1000 genomes]
rs2272526	0.88[CEU][hapmap];0.83[CHB][hapmap];0.89[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2272527	0.89[CEU][hapmap];0.80[CHB][hapmap];0.90[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2341025	0.80[EUR][1000 genomes]
rs2341578	0.81[CHB][hapmap]
rs28412607	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28451147	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28709062	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28832366	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35791987	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4291167	0.84[CEU][hapmap];0.84[JPT][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4496870	0.85[CEU][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs5022333	0.92[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs55878136	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs55933090	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56134531	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56234403	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56341242	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs57462209	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57704507	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs57733415	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs57743735	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58028517	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58498999	0.81[ASN][1000 genomes]
rs58601265	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs58748813	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58979693	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs59228270	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60268542	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60867986	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61605079	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6462121	0.86[JPT][hapmap]
rs6462126	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6462127	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6462128	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs67253031	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs67540761	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs68004656	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs68143552	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6947615	0.90[CEU][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6959706	0.81[JPT][hapmap]
rs6962132	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6966652	0.88[ASN][1000 genomes]
rs6971989	0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs73035954	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73035962	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73035977	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73038556	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73293551	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73671854	0.88[AMR][1000 genomes]
rs7779462	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7780340	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7787559	0.89[JPT][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7789656	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7791215	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7794992	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7795323	0.89[CEU][hapmap];0.84[CHB][hapmap];0.90[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7800962	0.85[JPT][hapmap]
rs7802868	0.81[ASN][1000 genomes]
rs7805283	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7805598	0.90[CEU][hapmap];0.85[JPT][hapmap];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7808972	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9638859	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9639598	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9654994	0.83[CHB][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap];0.90[ASN][1000 genomes]
rs9771445	0.90[CEU][hapmap];0.80[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018173	chr7:3258989-3879848	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv538660	chr7:3258989-3879848	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1016555	chr7:3298478-3872512	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538661	chr7:3298478-3872512	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2764026	chr7:3365002-3618361	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv916071	chr7:3423207-3697428	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1034716	chr7:3512406-3616155	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv887334	chr7:3531275-3635105	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv1023888	chr7:3539750-3638242	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1034298	chr7:3539750-3646251	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1029264	chr7:3549193-3622532	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv1032031	chr7:3554760-3609584	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv538675	chr7:3554760-3609584	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv1025623	chr7:3558521-3606640	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv1034671	chr7:3565156-3607294	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv538677	chr7:3565156-3607294	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv1028274	chr7:3565356-3607155	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv538678	chr7:3565356-3607155	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv830888	chr7:3577214-3776276	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
20	esv1840932	chr7:3585560-3618827	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv1792280	chr7:3592290-3668229	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv605907	chr7:3598581-3614784	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv1022135	chr7:3601840-3618349	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv1020806	chr7:3602348-3614788	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
25	esv2757205	chr7:3602348-3630349	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
26	esv2759501	chr7:3602348-3630349	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
27	nsv1017012	chr7:3602397-3638242	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
28	nsv538679	chr7:3602397-3638242	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
29	nsv605908	chr7:3605340-3615334	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
30	nsv605909	chr7:3605340-3638547	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3600600-3616600	Weak transcription	Gastric	stomach
2	chr7:3605200-3609000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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