Variant report

Variant	rs11014550
Chromosome Location	chr10:25722458-25722459
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 118 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs10399962	0.83[CEU][hapmap];0.92[CHB][hapmap];0.87[JPT][hapmap]
rs10508694	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10741075	0.86[JPT][hapmap]
rs10741077	1.00[JPT][hapmap]
rs10764539	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10764543	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs10828770	0.86[JPT][hapmap]
rs10828774	1.00[JPT][hapmap]
rs10828775	1.00[JPT][hapmap]
rs10828777	1.00[JPT][hapmap]
rs10828778	1.00[JPT][hapmap]
rs10828791	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs10828792	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs10828793	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs10828807	0.83[CEU][hapmap];0.84[CHB][hapmap];0.87[JPT][hapmap]
rs11014527	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs11014528	0.91[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs11014529	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs11014530	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs11014553	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs11014554	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11014558	0.88[CEU][hapmap];0.93[JPT][hapmap]
rs11014559	0.83[CEU][hapmap];0.92[CHB][hapmap];0.87[JPT][hapmap]
rs11014564	0.82[CEU][hapmap]
rs1122776	1.00[JPT][hapmap]
rs1148154	1.00[JPT][hapmap]
rs11818261	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12240665	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs12249852	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs12251868	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs12251917	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs12254479	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs12256851	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs12258671	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs12259043	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12259696	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12358447	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12762462	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12764415	0.82[CEU][hapmap]
rs12765005	0.83[CEU][hapmap]
rs12770990	0.83[CEU][hapmap]
rs12773262	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1329259	1.00[JPT][hapmap]
rs1329263	1.00[JPT][hapmap]
rs1329265	1.00[JPT][hapmap]
rs1340002	0.83[CHB][hapmap];0.93[JPT][hapmap]
rs1341963	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs1341964	1.00[JPT][hapmap]
rs1341966	1.00[JPT][hapmap]
rs1410932	1.00[JPT][hapmap]
rs1413397	1.00[JPT][hapmap]
rs1576317	1.00[JPT][hapmap]
rs1576320	0.93[JPT][hapmap]
rs1590836	1.00[JPT][hapmap]
rs1591249	1.00[JPT][hapmap]
rs1591250	0.93[JPT][hapmap]
rs1612200	1.00[JPT][hapmap]
rs1628986	1.00[JPT][hapmap]
rs16925850	0.94[CEU][hapmap];0.92[CHB][hapmap];0.88[JPT][hapmap]
rs16925877	0.83[CEU][hapmap]
rs1754251	1.00[JPT][hapmap]
rs1754253	0.92[JPT][hapmap]
rs1754260	1.00[JPT][hapmap]
rs1754268	1.00[JPT][hapmap]
rs1760716	1.00[JPT][hapmap]
rs1760718	1.00[JPT][hapmap]
rs1760727	1.00[JPT][hapmap]
rs1760728	1.00[JPT][hapmap]
rs1760733	1.00[JPT][hapmap]
rs1760758	1.00[JPT][hapmap]
rs1760759	1.00[JPT][hapmap]
rs1760762	1.00[JPT][hapmap]
rs1760763	1.00[JPT][hapmap]
rs1760766	1.00[JPT][hapmap]
rs1760767	1.00[JPT][hapmap]
rs1773608	1.00[JPT][hapmap]
rs1773612	1.00[JPT][hapmap]
rs1773614	1.00[JPT][hapmap]
rs1773616	1.00[JPT][hapmap]
rs1773617	1.00[JPT][hapmap]
rs1773618	1.00[JPT][hapmap]
rs1773622	1.00[JPT][hapmap]
rs1773623	1.00[JPT][hapmap]
rs1773625	0.93[JPT][hapmap]
rs1773649	1.00[JPT][hapmap]
rs1773650	1.00[JPT][hapmap]
rs1773689	0.85[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs1773690	0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs1855461	1.00[JPT][hapmap]
rs2795044	1.00[JPT][hapmap]
rs2807248	0.86[JPT][hapmap]
rs2807253	0.93[JPT][hapmap]
rs2807255	1.00[JPT][hapmap]
rs4351726	1.00[JPT][hapmap]
rs4431923	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs489052	1.00[JPT][hapmap]
rs489186	1.00[JPT][hapmap]
rs495338	1.00[JPT][hapmap]
rs495456	1.00[JPT][hapmap]
rs509285	1.00[JPT][hapmap]
rs516071	1.00[JPT][hapmap]
rs541206	0.94[JPT][hapmap]
rs543850	0.93[JPT][hapmap]
rs558947	0.86[JPT][hapmap]
rs573812	1.00[JPT][hapmap]
rs7079892	1.00[JPT][hapmap]
rs7094439	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs722537	0.87[JPT][hapmap]
rs824145	0.87[JPT][hapmap]
rs824146	0.86[JPT][hapmap]
rs824590	1.00[JPT][hapmap]
rs824592	1.00[JPT][hapmap]
rs824597	1.00[JPT][hapmap]
rs824598	1.00[JPT][hapmap];0.82[YRI][hapmap]
rs824599	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs862192	0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv2760120	chr10:25721094-25728594	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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