Variant report

Variant	rs10736017
Chromosome Location	chr12:44300037-44300038
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:44291890..44294959-chr12:44297148..44301402,3	MCF-7	breast:

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs1057486	0.92[ASN][1000 genomes]
rs10748378	1.00[ASN][1000 genomes]
rs10785462	1.00[ASN][1000 genomes]
rs10785463	1.00[ASN][1000 genomes]
rs10785466	1.00[ASN][1000 genomes]
rs10785468	0.81[ASN][1000 genomes]
rs10785469	0.91[ASN][1000 genomes]
rs10880573	0.87[ASN][1000 genomes]
rs10880578	0.91[ASN][1000 genomes]
rs10880585	1.00[ASN][1000 genomes]
rs11182293	0.94[ASN][1000 genomes]
rs11182324	1.00[ASN][1000 genomes]
rs11182325	1.00[ASN][1000 genomes]
rs1358705	0.94[ASN][1000 genomes]
rs1406787	0.94[ASN][1000 genomes]
rs1609548	1.00[ASN][1000 genomes]
rs1609549	0.94[ASN][1000 genomes]
rs1610291	1.00[ASN][1000 genomes]
rs1614042	0.94[ASN][1000 genomes]
rs1621279	0.94[ASN][1000 genomes]
rs1622590	0.94[ASN][1000 genomes]
rs1675756	0.94[ASN][1000 genomes]
rs1675758	0.94[ASN][1000 genomes]
rs1675764	0.94[ASN][1000 genomes]
rs1675765	0.94[ASN][1000 genomes]
rs1675766	0.80[EUR][1000 genomes]
rs1675767	0.94[ASN][1000 genomes]
rs1675769	0.94[ASN][1000 genomes]
rs1675781	0.97[ASN][1000 genomes]
rs1675785	0.97[ASN][1000 genomes]
rs1675787	0.94[ASN][1000 genomes]
rs1675789	0.94[ASN][1000 genomes]
rs1675790	0.94[ASN][1000 genomes]
rs1731421	0.80[AFR][1000 genomes]
rs1731423	0.94[ASN][1000 genomes]
rs1731427	0.97[AFR][1000 genomes];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1731429	0.94[AFR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1731430	0.94[ASN][1000 genomes]
rs1731431	0.94[ASN][1000 genomes]
rs1731432	0.94[ASN][1000 genomes]
rs1731434	0.94[ASN][1000 genomes]
rs1731447	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1731449	0.80[EUR][1000 genomes]
rs1731452	0.94[ASN][1000 genomes]
rs1731453	0.80[EUR][1000 genomes]
rs1731454	0.94[ASN][1000 genomes]
rs1731456	0.94[ASN][1000 genomes]
rs1731457	0.94[ASN][1000 genomes]
rs1731458	0.94[ASN][1000 genomes]
rs1731459	0.94[ASN][1000 genomes]
rs2219629	0.94[ASN][1000 genomes]
rs2407783	1.00[ASN][1000 genomes]
rs2447113	0.94[ASN][1000 genomes]
rs2614394	0.97[AFR][1000 genomes];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2699992	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs2951435	0.91[ASN][1000 genomes]
rs4238089	1.00[ASN][1000 genomes]
rs4238090	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4238091	1.00[ASN][1000 genomes]
rs4354753	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4363674	1.00[ASN][1000 genomes]
rs4469953	1.00[ASN][1000 genomes]
rs4537822	1.00[ASN][1000 genomes]
rs4572198	1.00[ASN][1000 genomes]
rs4572199	1.00[ASN][1000 genomes]
rs4609659	1.00[ASN][1000 genomes]
rs4768052	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4768053	0.92[ASN][1000 genomes]
rs4768534	0.85[AFR][1000 genomes]
rs4768538	1.00[ASN][1000 genomes]
rs4768543	0.92[ASN][1000 genomes]
rs5019975	1.00[ASN][1000 genomes]
rs7295151	1.00[ASN][1000 genomes]
rs7305609	0.94[ASN][1000 genomes]
rs73096934	0.94[ASN][1000 genomes]
rs7955615	1.00[ASN][1000 genomes]
rs7965240	0.86[ASN][1000 genomes]
rs7965330	0.86[ASN][1000 genomes]
rs7965635	0.80[EUR][1000 genomes]
rs7972025	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899048	chr12:44209423-44307888	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
2	nsv526719	chr12:44298417-44315762	Weak transcription Enhancers 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	chr12:44293800-44300800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr12:44298800-44307800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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