Variant report

Variant	rs17501869
Chromosome Location	chr10:45184927-45184928
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10508888	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11239222	0.84[EUR][1000 genomes]
rs11816488	0.96[EUR][1000 genomes]
rs12098746	0.87[EUR][1000 genomes]
rs12220526	0.84[EUR][1000 genomes]
rs12254934	0.93[EUR][1000 genomes]
rs12569566	0.96[EUR][1000 genomes]
rs12569855	0.96[EUR][1000 genomes]
rs12572644	0.96[EUR][1000 genomes]
rs12764414	0.96[EUR][1000 genomes]
rs12768956	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12771080	0.96[EUR][1000 genomes]
rs12772796	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12783832	0.87[EUR][1000 genomes]
rs12785099	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1383374	0.87[EUR][1000 genomes]
rs17156787	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17156829	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17502557	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1968850	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34093140	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34167921	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34586920	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34893515	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35018589	0.96[EUR][1000 genomes]
rs35054029	0.87[EUR][1000 genomes]
rs35125250	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35280741	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35392689	0.96[EUR][1000 genomes]
rs35878166	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35980365	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7069781	0.84[EUR][1000 genomes]
rs7070865	0.96[EUR][1000 genomes]
rs7084823	0.84[EUR][1000 genomes]
rs7094529	0.96[EUR][1000 genomes]
rs71494741	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71494742	0.96[EUR][1000 genomes]
rs71494744	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7897547	0.93[EUR][1000 genomes]
rs7903994	0.93[EUR][1000 genomes]
rs7912000	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7912289	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7916283	0.86[EUR][1000 genomes]
rs7919204	0.93[EUR][1000 genomes]
rs899888	0.93[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	esv2422287	chr10:45044161-45257684	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv831843	chr10:45084703-45280032	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45176200-45185800	Weak transcription	Aorta	Aorta
2	chr10:45184600-45185000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr10:45184600-45185000	Enhancers	Osteobl	bone

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