Variant report

Variant	rs11047852
Chromosome Location	chr12:25287965-25287966
allele	A/C
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:53)

rs_ID	r²[population]
rs10505960	0.80[AFR][1000 genomes]
rs10771169	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10771171	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10771175	0.82[ASN][1000 genomes]
rs10771176	0.83[ASN][1000 genomes]
rs10842469	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10842471	0.90[AFR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10842472	0.92[ASN][1000 genomes]
rs10842473	0.80[AFR][1000 genomes]
rs10842475	0.92[AFR][1000 genomes]
rs10842476	0.90[ASN][1000 genomes]
rs10842478	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10842483	0.90[ASN][1000 genomes]
rs10842488	0.83[ASN][1000 genomes]
rs10842490	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10842491	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10842492	0.85[AFR][1000 genomes]
rs10842495	0.83[ASN][1000 genomes]
rs11047854	0.92[AFR][1000 genomes]
rs11047855	0.92[AFR][1000 genomes]
rs11047856	0.92[AFR][1000 genomes]
rs11047858	0.92[ASN][1000 genomes]
rs11047862	0.90[ASN][1000 genomes]
rs11047865	0.82[AFR][1000 genomes]
rs11513449	0.85[AFR][1000 genomes]
rs12227966	0.83[ASN][1000 genomes]
rs12228638	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12367971	0.83[ASN][1000 genomes]
rs12424685	0.92[AFR][1000 genomes]
rs12818169	0.92[AFR][1000 genomes]
rs12828609	0.92[AFR][1000 genomes]
rs12830058	0.92[AFR][1000 genomes]
rs12830336	0.82[AFR][1000 genomes]
rs2220196	0.90[ASN][1000 genomes]
rs2291365	0.82[AFR][1000 genomes]
rs2352782	0.92[AFR][1000 genomes]
rs2352784	0.85[AFR][1000 genomes]
rs2883030	0.92[ASN][1000 genomes]
rs4313666	0.83[ASN][1000 genomes]
rs4559767	0.85[AFR][1000 genomes]
rs4589388	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4963850	0.82[AFR][1000 genomes]
rs55950027	0.83[ASN][1000 genomes]
rs61020746	0.87[AFR][1000 genomes]
rs6487456	0.82[AFR][1000 genomes]
rs6487458	0.92[ASN][1000 genomes]
rs7133904	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7135130	0.92[ASN][1000 genomes]
rs7303373	0.83[ASN][1000 genomes]
rs7956818	0.92[ASN][1000 genomes]
rs7971062	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7971288	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7973365	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469169	chr12:24692383-25357680	Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv557775	chr12:24692383-25357680	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv932477	chr12:24705151-25346677	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv1067577	chr12:24791283-25346677	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv529514	chr12:24791283-25346677	Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv1041218	chr12:24972019-25304356	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv557796	chr12:25266203-25306458	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv515612	chr12:25272027-25341177	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv557797	chr12:25272027-25341177	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv898922	chr12:25274593-25408047	Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 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	chr12:25263800-25288800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr12:25286800-25288000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr12:25286800-25304200	Weak transcription	Ovary	ovary

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