Variant report

Variant	rs10745446
Chromosome Location	chr12:87830464-87830465
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:87828977..87831928-chr12:87832715..87835394,2	MCF-7	breast:
2	chr12:87829514..87833509-chr12:87836513..87839734,3	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10735256	0.85[AMR][1000 genomes]
rs10735258	0.92[AMR][1000 genomes]
rs10735261	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10735262	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10735264	0.87[EUR][1000 genomes]
rs10745444	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10745448	0.87[EUR][1000 genomes]
rs10745449	0.87[EUR][1000 genomes]
rs10777033	0.92[AMR][1000 genomes]
rs10777042	1.00[AMR][1000 genomes]
rs10777043	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10777048	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10858592	0.85[AMR][1000 genomes]
rs10858598	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs10858599	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11104443	0.92[AMR][1000 genomes]
rs11104470	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1353484	0.87[EUR][1000 genomes]
rs1353486	0.87[EUR][1000 genomes]
rs1353487	0.87[EUR][1000 genomes]
rs1353488	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1390604	0.87[EUR][1000 genomes]
rs1390605	0.87[EUR][1000 genomes]
rs1496320	0.87[EUR][1000 genomes]
rs1496321	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2047306	0.87[EUR][1000 genomes]
rs2406753	0.83[AMR][1000 genomes]
rs2897518	0.85[AMR][1000 genomes]
rs4147490	0.83[AMR][1000 genomes]
rs4254148	0.85[AMR][1000 genomes]
rs4258454	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4269999	0.92[AMR][1000 genomes]
rs4300469	0.83[AMR][1000 genomes]
rs4303307	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4310691	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4319586	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4326883	0.92[AMR][1000 genomes]
rs4338623	0.83[AMR][1000 genomes]
rs4372533	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4402386	0.92[AMR][1000 genomes]
rs4442619	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4466916	0.92[AMR][1000 genomes]
rs4561282	0.92[AMR][1000 genomes]
rs4576908	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4590963	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4597138	1.00[AMR][1000 genomes]
rs4635161	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4842462	0.87[EUR][1000 genomes]
rs4842570	1.00[AMR][1000 genomes]
rs4842576	0.87[EUR][1000 genomes]
rs5005936	0.85[AMR][1000 genomes]
rs6538078	0.92[AMR][1000 genomes]
rs6538079	0.85[AMR][1000 genomes]
rs6538082	0.92[AMR][1000 genomes]
rs6538083	0.85[AMR][1000 genomes]
rs6538087	0.91[CEU][hapmap];0.83[AMR][1000 genomes]
rs6538088	0.91[CEU][hapmap];0.92[AMR][1000 genomes]
rs6538104	0.87[EUR][1000 genomes]
rs6538105	0.87[EUR][1000 genomes]
rs6538106	0.87[EUR][1000 genomes]
rs7305305	0.85[AMR][1000 genomes]
rs7311170	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7959041	0.87[EUR][1000 genomes]
rs7962840	0.92[AMR][1000 genomes]
rs7967687	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7969510	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7969855	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7970832	0.85[AMR][1000 genomes]
rs7974679	0.92[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430523	chr12:87757132-87865832	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv430525	chr12:87757132-87905532	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3329221	chr12:87785317-87833393	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv559701	chr12:87801947-87905878	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3350469	chr12:87802235-87844904	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:87822800-87833000	Weak transcription	A549	lung
2	chr12:87824800-87831400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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