Variant report

Variant	rs11115778
Chromosome Location	chr12:83783049-83783050
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:83078627..83080390-chr12:83781749..83784378,2	MCF-7	breast:
2	chr12:83079105..83081641-chr12:83780765..83784408,3	MCF-7	breast:
3	chr12:83398128..83399066-chr12:83782720..83783715,3	K562	blood:
4	chr12:83782814..83783717-chr20:57797390..57797949,2	MCF-7	breast:
5	chr12:83079259..83080112-chr12:83782817..83783839,5	MCF-7	breast:
6	chr12:83079542..83080051-chr12:83782752..83783696,2	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC59-7	chr12:83782251-83783300	ucscGeneNc_uc001szx_2

No data

Variant related genes	Relation type
ENSG00000179104	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10047542	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10047543	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10047574	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10047575	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs10778980	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10778981	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10778982	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10778983	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10778984	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10778985	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10778986	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10778987	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10778988	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10778989	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10778990	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs10778991	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs10778992	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs10862642	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10862643	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10862644	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10862645	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10862646	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10862647	0.95[AMR][1000 genomes]
rs10862650	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10862651	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs10862652	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10862653	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10862654	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10862656	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs10862659	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs11115755	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs11115759	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs11115760	0.93[AMR][1000 genomes]
rs11115764	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs11115765	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs11115766	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs11115768	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs11115772	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs11115773	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs11115777	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs12299063	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs12368213	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4269996	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4274267	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4346039	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4471519	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4506727	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4512929	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4520676	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs4526842	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4540901	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs4584655	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4988663	0.88[AMR][1000 genomes]
rs4988664	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs4988665	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7133909	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs7309196	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs7484480	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs7485438	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs7487330	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs7488808	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs7968688	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs8181772	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs8181788	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521849	chr12:83013783-83991479	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1042674	chr12:83620899-83942628	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv899353	chr12:83755861-83792347	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv899354	chr12:83755861-83813669	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83782800-83783200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:83782800-83783200	Enhancers	Pancreas	Pancrea
3	chr12:83783000-83783600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:83783000-83783600	Enhancers	Liver	Liver

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