Variant report

Variant	rs2673185
Chromosome Location	chr2:123834466-123834467
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	chr2:123828454..123831297-chr2:123833230..123835913,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000232740	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10178398	0.88[EUR][1000 genomes]
rs1154995	0.95[EUR][1000 genomes]
rs1160010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1160011	0.96[EUR][1000 genomes]
rs12620936	0.97[EUR][1000 genomes]
rs12996298	0.81[EUR][1000 genomes]
rs13005367	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13031371	0.83[CEU][hapmap];0.97[EUR][1000 genomes]
rs1395931	0.89[EUR][1000 genomes]
rs1507667	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1606802	0.89[EUR][1000 genomes]
rs188493	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2063800	0.81[EUR][1000 genomes]
rs2138170	0.85[EUR][1000 genomes]
rs2244129	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2248895	0.92[EUR][1000 genomes]
rs2419071	0.96[EUR][1000 genomes]
rs2458994	0.97[EUR][1000 genomes]
rs2661001	0.94[EUR][1000 genomes]
rs2661032	0.97[EUR][1000 genomes]
rs2661035	0.95[EUR][1000 genomes]
rs2661036	0.90[EUR][1000 genomes]
rs2661041	0.95[EUR][1000 genomes]
rs2661043	0.94[EUR][1000 genomes]
rs2661044	0.94[EUR][1000 genomes]
rs2661045	0.94[EUR][1000 genomes]
rs2673182	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2673187	0.96[EUR][1000 genomes]
rs2673188	0.97[EUR][1000 genomes]
rs2673189	0.97[EUR][1000 genomes]
rs2673194	0.95[EUR][1000 genomes]
rs2673196	0.94[EUR][1000 genomes]
rs2900804	0.95[EUR][1000 genomes]
rs299536	0.96[EUR][1000 genomes]
rs299539	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs299540	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs299542	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs299544	0.94[CEU][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs299545	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs299546	0.83[CEU][hapmap];0.97[EUR][1000 genomes]
rs299548	0.83[CEU][hapmap];0.97[EUR][1000 genomes]
rs299549	0.97[EUR][1000 genomes]
rs299550	0.97[EUR][1000 genomes]
rs299551	0.84[CEU][hapmap];0.97[EUR][1000 genomes]
rs299553	0.97[EUR][1000 genomes]
rs299560	0.90[EUR][1000 genomes]
rs299561	0.89[EUR][1000 genomes]
rs299562	0.91[EUR][1000 genomes]
rs36131743	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4848824	0.90[EUR][1000 genomes]
rs6731851	0.81[EUR][1000 genomes]
rs6734712	0.81[EUR][1000 genomes]
rs6747893	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9636359	0.89[EUR][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	nsv492280	chr2:123447662-123973577	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2760647	chr2:123678437-124619697	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1010200	chr2:123816326-123887210	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv961349	chr2:123827896-123840926	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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