Variant report

Variant	rs10508714
Chromosome Location	chr10:26470436-26470437
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:26465564..26468022-chr10:26468180..26471096,2	K562	blood:

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10082469	0.90[EUR][1000 genomes]
rs10764598	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10828953	0.90[EUR][1000 genomes]
rs11014924	0.80[EUR][1000 genomes]
rs11014925	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs11014934	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs11014976	0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs11014979	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11014984	0.92[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11014993	0.86[CHB][hapmap];0.91[YRI][hapmap];0.83[ASN][1000 genomes]
rs11593041	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11598861	0.88[CEU][hapmap];0.90[EUR][1000 genomes]
rs11819592	0.90[EUR][1000 genomes]
rs12246202	0.89[EUR][1000 genomes]
rs12247347	0.83[ASN][1000 genomes]
rs12247650	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs12252534	0.81[EUR][1000 genomes]
rs12258401	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12258453	0.92[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.87[YRI][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12262670	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs12262728	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12263990	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs12266221	0.85[EUR][1000 genomes]
rs12266309	0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs12267297	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs12411554	0.81[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs12572400	0.83[CEU][hapmap];0.82[EUR][1000 genomes]
rs12572695	0.80[EUR][1000 genomes]
rs12766250	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs12768268	0.81[EUR][1000 genomes]
rs12770421	0.87[CEU][hapmap];0.84[EUR][1000 genomes]
rs1339808	0.84[CEU][hapmap]
rs1339812	0.83[CEU][hapmap]
rs1339813	0.81[EUR][1000 genomes]
rs1339814	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs1339815	0.84[CEU][hapmap];0.82[EUR][1000 genomes]
rs1339816	0.83[CEU][hapmap];0.82[EUR][1000 genomes]
rs1342320	0.92[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.81[YRI][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1402437	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs1416860	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs1546701	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs17813720	0.88[CEU][hapmap]
rs1856603	0.81[EUR][1000 genomes]
rs1915478	0.81[EUR][1000 genomes]
rs1935484	0.81[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs1949616	0.81[EUR][1000 genomes]
rs2090797	0.84[CEU][hapmap];0.88[EUR][1000 genomes]
rs2096176	0.81[CHB][hapmap];0.95[JPT][hapmap]
rs2176941	0.90[EUR][1000 genomes]
rs2368158	0.81[CHB][hapmap];0.95[JPT][hapmap]
rs35137356	0.87[EUR][1000 genomes]
rs3740231	0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs3740232	0.92[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.87[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3758447	0.81[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs3758448	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3758449	0.95[JPT][hapmap]
rs4539209	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6482531	0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs6482532	0.82[CHB][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs7072451	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7079780	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7081905	0.92[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7084000	0.80[ASN][1000 genomes]
rs7085103	0.81[CHB][hapmap];0.95[JPT][hapmap]
rs7091566	0.80[CHB][hapmap];0.84[JPT][hapmap]
rs7093989	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs7095559	0.88[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.87[YRI][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7096646	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7476324	0.95[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7895318	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs7895734	0.90[EUR][1000 genomes]
rs7899450	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs7899567	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs7913502	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs7920488	0.83[ASN][1000 genomes]
rs9629915	0.86[EUR][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	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26440800-26473400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26464600-26478000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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