Variant report

Variant	rs2665549
Chromosome Location	chr3:68560669-68560670
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs1039971	0.85[YRI][hapmap]
rs1039972	0.86[YRI][hapmap]
rs1039974	0.81[YRI][hapmap]
rs1158308	0.82[YRI][hapmap]
rs13068116	0.84[AMR][1000 genomes]
rs13080569	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13080937	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13095473	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13096988	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1355522	0.82[YRI][hapmap]
rs1355527	0.90[YRI][hapmap]
rs1355528	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1398066	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1511889	0.86[YRI][hapmap]
rs1511890	0.80[YRI][hapmap]
rs1511893	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1511894	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1511895	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1511896	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1511899	0.81[YRI][hapmap]
rs1511901	0.86[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs1511902	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1511903	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1511904	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1511908	0.86[YRI][hapmap]
rs1533155	0.90[YRI][hapmap]
rs1533156	0.86[YRI][hapmap]
rs1606243	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17242840	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1849228	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1849229	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1849230	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1849231	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1849232	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1849236	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1858375	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1858376	0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1858377	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1912852	0.81[YRI][hapmap]
rs1912854	1.00[YRI][hapmap]
rs1912855	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2015578	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2137181	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2665530	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2665531	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2665532	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2665533	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2665535	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2665536	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2665537	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2665538	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2665540	0.81[YRI][hapmap]
rs2668156	0.95[YRI][hapmap]
rs2668159	1.00[YRI][hapmap]
rs2668161	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2668162	0.81[YRI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2668163	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2668165	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2668166	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2668167	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2668168	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2668169	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2668170	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4855339	0.85[YRI][hapmap]
rs58726756	0.84[AMR][1000 genomes]
rs6549128	0.81[YRI][hapmap]
rs6549130	0.81[YRI][hapmap]
rs6774423	0.86[YRI][hapmap]
rs9310104	0.81[YRI][hapmap]
rs9310105	0.90[YRI][hapmap]
rs983191	0.82[YRI][hapmap]
rs9856419	0.86[YRI][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	esv1832396	chr3:68478762-68641509	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv876929	chr3:68508137-68565824	ZNF genes & repeats Enhancers Weak transcription	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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