Variant report

Variant	rs2487819
Chromosome Location	chr10:25757452-25757453
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:25756226..25758820-chr10:25766240..25768212,2	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10508695	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs10508696	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs1069531	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11014576	0.95[ASN][1000 genomes]
rs12415532	0.89[CHB][hapmap];0.86[ASN][1000 genomes]
rs12763436	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12766947	0.95[ASN][1000 genomes]
rs12770449	0.99[ASN][1000 genomes]
rs12770880	0.99[ASN][1000 genomes]
rs12778509	0.95[ASN][1000 genomes]
rs1329255	0.85[CEU][hapmap];0.92[MEX][hapmap]
rs1329256	0.84[CEU][hapmap]
rs1329257	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1360123	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1361634	0.92[CEU][hapmap];1.00[CHB][hapmap];0.85[GIH][hapmap];0.88[MEX][hapmap];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1410931	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1590833	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs1592137	0.88[CHB][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1620326	0.86[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.89[TSI][hapmap];0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1773636	0.91[CEU][hapmap];0.92[YRI][hapmap];0.98[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs1773637	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1928365	0.85[CEU][hapmap]
rs2211344	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2480348	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2480349	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2987832	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2987833	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2987834	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2987835	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2987836	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2987838	0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2987839	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3005182	0.85[CEU][hapmap];0.80[MEX][hapmap]
rs3005189	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3005191	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[GIH][hapmap];0.88[MEX][hapmap];0.84[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3005193	1.00[CEU][hapmap];0.86[CHB][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3005194	0.88[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs34535236	0.95[ASN][1000 genomes]
rs36146927	0.90[ASN][1000 genomes]
rs4408231	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4545439	0.89[CHB][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs4630196	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57048226	0.95[ASN][1000 genomes]
rs66516873	0.95[ASN][1000 genomes]
rs67290477	0.95[ASN][1000 genomes]
rs67616835	0.95[ASN][1000 genomes]
rs702977	0.94[EUR][1000 genomes]
rs702980	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[GIH][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.93[TSI][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7075106	0.88[ASN][1000 genomes]
rs7084979	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs7085111	0.95[ASN][1000 genomes]
rs7086959	0.88[ASN][1000 genomes]
rs7089568	0.92[ASN][1000 genomes]
rs824588	0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[YRI][hapmap];0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs824589	0.96[CEU][hapmap];0.91[GIH][hapmap];0.89[TSI][hapmap];0.94[EUR][1000 genomes]
rs824607	0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[GIH][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs824608	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs824609	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs824610	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[GIH][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.91[TSI][hapmap];0.94[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25755400-25757800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr10:25755800-25757800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr10:25756400-25758200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr10:25756400-25758200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr10:25756600-25758000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr10:25756800-25757600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr10:25756800-25757600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr10:25756800-25757800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr10:25756800-25758000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr10:25756800-25775000	Weak transcription	K562	blood
11	chr10:25757200-25759400	Weak transcription	Placenta	Placenta
12	chr10:25757200-25769600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr10:25757400-25757600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr10:25757400-25757600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr10:25757400-25758000	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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