Variant report

Variant	rs1756622
Chromosome Location	chr14:56496434-56496435
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	chr14:56489100..56490654-chr14:56494380..56496682,2	MCF-7	breast:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1188188	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1188194	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1188196	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1188198	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1188199	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1188200	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1188203	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs1188204	0.82[CEU][hapmap]
rs1201387	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1211177	0.93[CEU][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1211455	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1212200	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1212974	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12432868	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1480650	0.91[ASN][1000 genomes]
rs1480657	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1480658	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1480659	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1623669	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1630156	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1679800	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1679801	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1679807	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1679809	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1679810	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1679811	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1756624	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1756625	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1756628	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1756630	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1756631	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1952892	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60269373	0.87[EUR][1000 genomes]
rs922655	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34106	chr14:56346245-56550642	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr14:56492400-56497000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:56494200-56496800	Enhancers	Psoas Muscle	Psoas
3	chr14:56495000-56496800	Enhancers	Aorta	Aorta
4	chr14:56496400-56496600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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