Variant report

Variant	rs12572782
Chromosome Location	chr10:18654086-18654087
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10734050	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10734051	0.88[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10741040	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10741042	0.96[ASN][1000 genomes]
rs10764443	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10764447	0.84[CEU][hapmap];0.96[ASN][1000 genomes]
rs10828592	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10828605	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10828606	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10828607	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10828616	0.92[ASW][hapmap];0.85[CEU][hapmap];0.85[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.86[JPT][hapmap];0.81[MKK][hapmap];0.88[ASN][1000 genomes]
rs10828617	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11013859	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11013862	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11013865	0.92[ASW][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11013889	0.81[AFR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12356676	0.82[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];0.93[TSI][hapmap];0.84[ASN][1000 genomes]
rs1325991	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16917217	0.84[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.92[MKK][hapmap];0.92[TSI][hapmap];0.81[AFR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1750479	0.86[CEU][hapmap];0.86[EUR][1000 genomes]
rs17539088	0.84[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.92[MKK][hapmap];0.92[TSI][hapmap];0.81[AFR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1926028	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61839222	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61839226	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6482360	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7072365	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7085825	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7099729	0.92[ASW][hapmap];0.81[CEU][hapmap];0.85[CHB][hapmap];0.92[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs7894616	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7898684	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7901058	0.95[ASN][1000 genomes]
rs7901640	0.87[CHD][hapmap]
rs7904974	1.00[CEU][hapmap];0.80[YRI][hapmap];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7907743	0.82[CHB][hapmap];0.82[JPT][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7908718	0.81[CEU][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs7911051	0.93[ASN][1000 genomes]
rs7911542	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7919691	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7920123	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9645525	0.85[CHB][hapmap]

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	nsv1046458	chr10:18629603-18683860	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island	1 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	chr10:18639600-18661400	Weak transcription	Aorta	Aorta
2	chr10:18652400-18654800	Weak transcription	Ovary	ovary
3	chr10:18652400-18667400	Weak transcription	Left Ventricle	heart
4	chr10:18653800-18654400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr10:18653800-18654800	Enhancers	Fetal Heart	heart
6	chr10:18654000-18654600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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