Variant report

Variant	rs10824012
Chromosome Location	chr10:53827643-53827644
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10762551	1.00[ASN][1000 genomes]
rs10762552	1.00[ASN][1000 genomes]
rs10824011	1.00[ASN][1000 genomes]
rs10824014	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10824015	1.00[ASN][1000 genomes]
rs10824016	1.00[ASN][1000 genomes]
rs10824017	1.00[ASN][1000 genomes]
rs10824018	1.00[ASN][1000 genomes]
rs10824019	1.00[ASN][1000 genomes]
rs10824020	1.00[ASN][1000 genomes]
rs10824022	1.00[ASN][1000 genomes]
rs10824023	1.00[ASN][1000 genomes]
rs11000668	1.00[ASN][1000 genomes]
rs11000673	1.00[ASN][1000 genomes]
rs11000674	1.00[ASN][1000 genomes]
rs11000675	1.00[ASN][1000 genomes]
rs11000677	1.00[ASN][1000 genomes]
rs11000678	1.00[ASN][1000 genomes]
rs11000679	1.00[ASN][1000 genomes]
rs11000680	1.00[ASN][1000 genomes]
rs11000681	1.00[ASN][1000 genomes]
rs11000684	1.00[ASN][1000 genomes]
rs11000685	1.00[ASN][1000 genomes]
rs11000686	1.00[ASN][1000 genomes]
rs11000687	1.00[ASN][1000 genomes]
rs11000688	1.00[ASN][1000 genomes]
rs11000689	1.00[ASN][1000 genomes]
rs11000690	1.00[ASN][1000 genomes]
rs11000691	1.00[ASN][1000 genomes]
rs11000692	1.00[ASN][1000 genomes]
rs11000693	0.98[ASN][1000 genomes]
rs11000694	1.00[ASN][1000 genomes]
rs11000699	1.00[ASN][1000 genomes]
rs11000704	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11000705	1.00[ASN][1000 genomes]
rs11000712	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11000713	1.00[ASN][1000 genomes]
rs12218769	0.96[ASN][1000 genomes]
rs12220039	1.00[ASN][1000 genomes]
rs12413063	1.00[ASN][1000 genomes]
rs12774871	0.85[EUR][1000 genomes]
rs12782457	1.00[ASN][1000 genomes]
rs1903954	1.00[ASN][1000 genomes]
rs1904026	1.00[ASN][1000 genomes]
rs1904028	1.00[ASN][1000 genomes]
rs1904030	1.00[ASN][1000 genomes]
rs1904031	1.00[ASN][1000 genomes]
rs34229993	0.98[ASN][1000 genomes]
rs5013005	1.00[ASN][1000 genomes]
rs72803121	1.00[ASN][1000 genomes]
rs72803122	1.00[ASN][1000 genomes]
rs72803123	0.98[ASN][1000 genomes]
rs72803124	1.00[ASN][1000 genomes]
rs7899949	0.96[ASN][1000 genomes]
rs7900083	1.00[ASN][1000 genomes]
rs7900087	1.00[ASN][1000 genomes]
rs7900093	1.00[ASN][1000 genomes]
rs7917109	0.96[ASN][1000 genomes]
rs7920290	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045692	chr10:53301450-54086823	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	esv2750961	chr10:53726294-54010594	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv532194	chr10:53746620-54735550	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1040754	chr10:53758289-53845925	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv550873	chr10:53811431-53838761	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv550874	chr10:53816171-53841105	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
7	esv9317	chr10:53827417-53828235	Weak transcription	n/a	n/a	inside rSNPs	n/a
8	esv3500729	chr10:53827546-53828099	Weak transcription	n/a	n/a	inside rSNPs	n/a
9	esv3370044	chr10:53827550-53828072	Weak transcription	n/a	n/a	inside rSNPs	n/a
10	esv3513708	chr10:53827558-53828094	Weak transcription	n/a	n/a	inside rSNPs	n/a
11	esv3513706	chr10:53827592-53828022	Weak transcription	n/a	n/a	inside rSNPs	n/a
12	esv3513704	chr10:53827603-53828033	Weak transcription	n/a	n/a	inside rSNPs	n/a
13	esv3500840	chr10:53827610-53828070	Weak transcription	n/a	n/a	inside rSNPs	n/a
14	esv3513705	chr10:53827612-53828038	Weak transcription	n/a	n/a	inside rSNPs	n/a
15	esv3500952	chr10:53827616-53828018	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:53814400-53842800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr10:53817400-53830000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr10:53821000-53828600	Weak transcription	Lung	lung
4	chr10:53824000-53838200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr10:53824200-53830200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr10:53824200-53835200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr10:53824400-53846200	Weak transcription	Aorta	Aorta
8	chr10:53824800-53831000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr10:53824800-53833000	Weak transcription	Psoas Muscle	Psoas
10	chr10:53825200-53830600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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