Variant report

Variant	rs1361634
Chromosome Location	chr10:25755801-25755802
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10508695	1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10508696	1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1069531	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11014576	0.99[ASN][1000 genomes]
rs12415532	0.89[CHB][hapmap];0.89[CHD][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs12763436	1.00[CHB][hapmap];0.92[CHD][hapmap];0.95[ASN][1000 genomes]
rs12766947	0.99[ASN][1000 genomes]
rs12770449	0.95[ASN][1000 genomes]
rs12770880	0.95[ASN][1000 genomes]
rs12778509	0.99[ASN][1000 genomes]
rs1329255	0.85[CEU][hapmap];0.92[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1329256	0.84[CEU][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1329257	0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1360123	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1410931	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1590833	0.89[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes]
rs1592137	0.88[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs1620326	0.89[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1773636	0.91[CEU][hapmap];0.87[EUR][1000 genomes]
rs1773637	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1928365	0.85[CEU][hapmap];0.84[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2211344	0.80[EUR][1000 genomes]
rs2480348	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2480349	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2487819	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]
rs2987832	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987833	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987834	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987835	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987836	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987838	0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987839	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987840	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3005181	0.83[ASN][1000 genomes]
rs3005182	0.85[CEU][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs3005187	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3005189	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3005191	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3005193	0.91[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3005194	0.85[EUR][1000 genomes]
rs3123901	0.83[ASN][1000 genomes]
rs34535236	0.99[ASN][1000 genomes]
rs36146927	0.94[ASN][1000 genomes]
rs4408231	0.84[EUR][1000 genomes]
rs4545439	0.89[CHB][hapmap];0.89[CHD][hapmap];0.86[ASN][1000 genomes]
rs57048226	0.99[ASN][1000 genomes]
rs66516873	0.99[ASN][1000 genomes]
rs67290477	0.99[ASN][1000 genomes]
rs67616835	0.99[ASN][1000 genomes]
rs702977	0.83[EUR][1000 genomes]
rs702980	0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7075106	0.92[ASN][1000 genomes]
rs7084979	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7085111	0.99[ASN][1000 genomes]
rs7086959	0.92[ASN][1000 genomes]
rs7089568	0.96[ASN][1000 genomes]
rs824588	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824589	0.96[CEU][hapmap];0.81[GIH][hapmap];0.86[EUR][1000 genomes]
rs824607	0.89[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.80[TSI][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824608	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824609	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824610	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.86[EUR][1000 genomes];1.00[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:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25754600-25756000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr10:25755000-25756400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:25755000-25757200	Strong transcription	Cortex derived primary cultured neurospheres	brain
4	chr10:25755400-25756400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr10:25755400-25757800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr10:25755600-25756000	Enhancers	Placenta	Placenta
7	chr10:25755600-25756800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr10:25755800-25756000	Flanking Active TSS	K562	blood
9	chr10:25755800-25756800	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr10:25755800-25757400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr10:25755800-25757800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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