Variant report

Variant	rs2677028
Chromosome Location	chr6:64129512-64129513
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 143 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:141)

rs_ID	r²[population]
rs1010057	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1320419	1.00[EUR][1000 genomes]
rs1404779	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1464865	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1464866	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1525354	1.00[EUR][1000 genomes]
rs1525355	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];1.00[EUR][1000 genomes]
rs1525357	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs1608812	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1619321	1.00[EUR][1000 genomes]
rs1621804	1.00[EUR][1000 genomes]
rs1625205	1.00[EUR][1000 genomes]
rs1628449	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1631333	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1711897	1.00[EUR][1000 genomes]
rs1711898	1.00[EUR][1000 genomes]
rs1711899	0.95[EUR][1000 genomes]
rs1711900	0.90[EUR][1000 genomes]
rs1711901	1.00[EUR][1000 genomes]
rs1711902	1.00[EUR][1000 genomes]
rs1711903	0.95[EUR][1000 genomes]
rs1711904	1.00[EUR][1000 genomes]
rs1711906	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];1.00[EUR][1000 genomes]
rs1711912	1.00[EUR][1000 genomes]
rs1711913	1.00[EUR][1000 genomes]
rs1711914	1.00[EUR][1000 genomes]
rs1711915	1.00[EUR][1000 genomes]
rs1711918	1.00[EUR][1000 genomes]
rs1711919	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1711927	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1711928	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1723497	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1723498	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1723499	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1723500	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1723502	0.90[EUR][1000 genomes]
rs1723503	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];1.00[EUR][1000 genomes]
rs1723504	0.95[EUR][1000 genomes]
rs1723506	0.90[EUR][1000 genomes]
rs1723507	0.90[EUR][1000 genomes]
rs1723508	0.95[EUR][1000 genomes]
rs1723527	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1723528	0.91[EUR][1000 genomes]
rs1723531	1.00[EUR][1000 genomes]
rs1741780	1.00[EUR][1000 genomes]
rs1741782	0.95[EUR][1000 genomes]
rs1741783	1.00[EUR][1000 genomes]
rs1741784	0.95[EUR][1000 genomes]
rs1741786	1.00[EUR][1000 genomes]
rs1741787	1.00[EUR][1000 genomes]
rs1741788	1.00[EUR][1000 genomes]
rs1741789	1.00[EUR][1000 genomes]
rs1741790	1.00[EUR][1000 genomes]
rs1741799	0.95[EUR][1000 genomes]
rs1741802	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1741805	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1741810	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1741813	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];1.00[EUR][1000 genomes]
rs1779745	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1779749	0.92[ASN][1000 genomes]
rs1779753	1.00[EUR][1000 genomes]
rs1779755	1.00[EUR][1000 genomes]
rs1779756	1.00[EUR][1000 genomes]
rs1779757	1.00[EUR][1000 genomes]
rs1779758	1.00[EUR][1000 genomes]
rs1779760	1.00[EUR][1000 genomes]
rs1857565	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1936532	1.00[EUR][1000 genomes]
rs2005098	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[EUR][1000 genomes]
rs2474908	1.00[EUR][1000 genomes]
rs2622277	1.00[CHB][hapmap]
rs2622306	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2622308	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2677021	0.95[EUR][1000 genomes]
rs2677022	1.00[EUR][1000 genomes]
rs2677023	1.00[EUR][1000 genomes]
rs2677024	0.91[EUR][1000 genomes]
rs2677026	1.00[EUR][1000 genomes]
rs2677027	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];1.00[EUR][1000 genomes]
rs2677029	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2753064	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2753065	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2753069	1.00[EUR][1000 genomes]
rs2753070	1.00[EUR][1000 genomes]
rs2753071	1.00[EUR][1000 genomes]
rs2753072	1.00[EUR][1000 genomes]
rs2753073	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2753074	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2800019	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2800020	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2800021	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2800024	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2800025	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2800029	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2800031	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2800034	1.00[EUR][1000 genomes]
rs2800035	1.00[EUR][1000 genomes]
rs2800036	1.00[EUR][1000 genomes]
rs4710426	1.00[EUR][1000 genomes]
rs56212786	0.84[AMR][1000 genomes]
rs59943612	0.85[EUR][1000 genomes]
rs60505637	0.85[EUR][1000 genomes]
rs61229307	0.85[EUR][1000 genomes]
rs6454169	1.00[EUR][1000 genomes]
rs6933112	1.00[EUR][1000 genomes]
rs732948	1.00[EUR][1000 genomes]
rs7381742	0.95[EUR][1000 genomes]
rs7382020	1.00[EUR][1000 genomes]
rs7750785	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7752941	1.00[EUR][1000 genomes]
rs7757686	1.00[EUR][1000 genomes]
rs7758841	1.00[EUR][1000 genomes]
rs7761720	0.90[EUR][1000 genomes]
rs7767012	0.84[AMR][1000 genomes]
rs7771677	1.00[EUR][1000 genomes]
rs7771703	0.90[EUR][1000 genomes]
rs824373	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824374	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824375	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824376	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824377	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824378	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824379	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824380	1.00[EUR][1000 genomes]
rs824381	1.00[EUR][1000 genomes]
rs824383	1.00[EUR][1000 genomes]
rs824385	1.00[EUR][1000 genomes]
rs824387	1.00[EUR][1000 genomes]
rs824388	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs824390	1.00[EUR][1000 genomes]
rs824391	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs824392	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs824393	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs824394	1.00[EUR][1000 genomes]
rs850830	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs860349	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs861113	1.00[EUR][1000 genomes]
rs865415	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs865416	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs940741	1.00[EUR][1000 genomes]
rs9767041	1.00[EUR][1000 genomes]

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	nsv1019831	chr6:63279677-64230736	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv538270	chr6:63682752-64147241	Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64128200-64131200	Enhancers	HepG2	liver
2	chr6:64128400-64129800	Enhancers	Primary B cells from cord blood	blood
3	chr6:64128600-64129600	Enhancers	Liver	Liver
4	chr6:64128800-64129600	Enhancers	GM12878-XiMat	blood
5	chr6:64129200-64130200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr6:64129400-64130200	Weak transcription	A549	lung

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