Variant report

Variant	rs2913878
Chromosome Location	chr5:151251888-151251889
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 146 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10044368	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs10050657	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10062169	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10065313	0.81[ASN][1000 genomes]
rs10075101	0.80[EUR][1000 genomes]
rs10078632	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10079787	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1042877	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs10463320	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10476776	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10476778	0.83[EUR][1000 genomes]
rs1062177	0.81[CHB][hapmap]
rs11167557	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11167559	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11954338	0.82[EUR][1000 genomes]
rs12108921	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12109022	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12109585	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12518238	0.80[ASN][1000 genomes]
rs12653926	0.80[ASN][1000 genomes]
rs12658422	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1366238	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1428159	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1428160	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1433041	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs1549920	0.81[CHB][hapmap]
rs17741826	0.82[CHB][hapmap]
rs2033212	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2347597	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs2913879	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2913881	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2913882	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2913888	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2913889	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2913892	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2913893	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2913894	1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2915822	0.81[CHB][hapmap]
rs2915826	0.81[CHB][hapmap]
rs2915827	0.82[CHB][hapmap]
rs2915868	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs2915872	0.92[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs2915876	0.81[CHB][hapmap]
rs2915878	0.81[CHB][hapmap]
rs2915879	0.82[CHB][hapmap]
rs2915880	0.82[CHB][hapmap]
rs2915885	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2915886	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs2915888	1.00[CEU][hapmap];0.87[CHB][hapmap];0.88[JPT][hapmap]
rs2915890	0.95[CEU][hapmap];0.87[CHB][hapmap];0.88[JPT][hapmap];0.81[EUR][1000 genomes]
rs2915891	0.80[EUR][1000 genomes]
rs2915892	0.80[EUR][1000 genomes]
rs2915893	0.80[EUR][1000 genomes]
rs2915894	0.80[EUR][1000 genomes]
rs2964570	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs2964574	0.81[CHB][hapmap]
rs2964584	0.81[CHB][hapmap]
rs2964587	0.82[CHB][hapmap]
rs2964591	0.81[CHB][hapmap]
rs2964592	0.81[CHB][hapmap]
rs2964596	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2964597	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2964599	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2964601	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2964603	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2964604	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2964606	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2964610	0.81[EUR][1000 genomes]
rs2964611	0.80[EUR][1000 genomes]
rs2964613	0.80[EUR][1000 genomes]
rs35692301	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4075273	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4076138	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4259159	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4331885	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4360031	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4362933	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4379180	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4419575	0.82[EUR][1000 genomes]
rs4472253	0.80[EUR][1000 genomes]
rs4478307	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4510568	0.82[EUR][1000 genomes]
rs4541649	0.83[EUR][1000 genomes]
rs4555782	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4571461	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs4594844	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4629583	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4629586	0.80[EUR][1000 genomes]
rs62394144	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62394155	0.80[ASN][1000 genomes]
rs6579897	0.82[CHB][hapmap]
rs6579906	0.83[EUR][1000 genomes]
rs6579908	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6579909	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6863833	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6863837	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6868371	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6870491	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6878691	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6892117	0.92[ASN][1000 genomes]
rs6896518	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6896664	0.92[ASN][1000 genomes]
rs72802219	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7341167	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7702751	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7711609	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7711771	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7712779	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7715874	0.80[EUR][1000 genomes]
rs7719617	0.92[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap]
rs7720579	0.80[EUR][1000 genomes]
rs7725327	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7728956	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7729026	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7733241	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7734314	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs892006	0.81[CHB][hapmap]
rs9324712	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9324714	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1808837	chr5:151238149-151260215	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv1807514	chr5:151242208-151252867	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv1807896	chr5:151242208-151252867	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1808791	chr5:151242208-151252867	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1808872	chr5:151242208-151252867	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv3487128	chr5:151247859-151254357	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3471109	chr5:151248159-151252657	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3487127	chr5:151248309-151254207	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3487129	chr5:151248309-151254207	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv11199	chr5:151249350-151252921	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv1805240	chr5:151249408-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv1807490	chr5:151249408-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv1808128	chr5:151249408-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv1811714	chr5:151249408-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv1812706	chr5:151249408-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv1813297	chr5:151249408-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3471110	chr5:151249859-151252657	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3471107	chr5:151249859-151254957	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
19	esv1805196	chr5:151250248-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv1806540	chr5:151250248-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv1808206	chr5:151250248-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv1809796	chr5:151250248-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
23	esv1810176	chr5:151250248-151252867	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
24	esv1811127	chr5:151250248-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv1811556	chr5:151250248-151252867	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
26	esv1813291	chr5:151250248-151252867	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
27	nsv600039	chr5:151250731-151252867	Enhancers Weak transcription	n/a	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	chr5:151235200-151264200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:151250000-151252200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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