Variant report

Variant	rs4651050
Chromosome Location	chr1:179717539-179717540
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:179715653..179718045-chr1:179722223..179724406,2	MCF-7	breast:
2	chr1:179712622..179714301-chr1:179716150..179718228,2	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1052447	0.96[ASN][1000 genomes]
rs10798718	0.96[ASN][1000 genomes]
rs10798719	0.96[ASN][1000 genomes]
rs10798720	0.96[ASN][1000 genomes]
rs10798721	0.96[ASN][1000 genomes]
rs10913874	0.96[ASN][1000 genomes]
rs10913876	0.96[ASN][1000 genomes]
rs10913877	0.96[ASN][1000 genomes]
rs10913878	0.96[ASN][1000 genomes]
rs10913879	0.96[ASN][1000 genomes]
rs12047821	0.95[ASN][1000 genomes]
rs12408874	0.96[ASN][1000 genomes]
rs12408882	0.96[ASN][1000 genomes]
rs2245195	0.96[ASN][1000 genomes]
rs2245610	0.82[ASN][1000 genomes]
rs2245702	0.82[ASN][1000 genomes]
rs2318389	0.96[ASN][1000 genomes]
rs2454193	0.86[ASN][1000 genomes]
rs2454195	0.96[ASN][1000 genomes]
rs2454196	0.96[ASN][1000 genomes]
rs2454197	0.84[ASN][1000 genomes]
rs2487739	0.94[ASN][1000 genomes]
rs2487740	0.96[ASN][1000 genomes]
rs2504032	0.85[ASN][1000 genomes]
rs2504033	0.85[ASN][1000 genomes]
rs2504035	0.82[ASN][1000 genomes]
rs2504038	0.82[ASN][1000 genomes]
rs2504039	0.96[ASN][1000 genomes]
rs2504040	0.96[ASN][1000 genomes]
rs2504041	0.96[ASN][1000 genomes]
rs2504042	0.96[ASN][1000 genomes]
rs2504043	0.82[ASN][1000 genomes]
rs2504048	0.82[ASN][1000 genomes]
rs2504049	0.82[ASN][1000 genomes]
rs2504053	0.90[ASN][1000 genomes]
rs3845381	0.96[ASN][1000 genomes]
rs3845382	0.92[ASN][1000 genomes]
rs3845383	0.92[ASN][1000 genomes]
rs3856045	0.96[ASN][1000 genomes]
rs3909014	0.96[ASN][1000 genomes]
rs3909015	0.96[ASN][1000 genomes]
rs4269737	0.87[ASN][1000 genomes]
rs4469684	0.96[ASN][1000 genomes]
rs4511077	0.96[ASN][1000 genomes]
rs60556788	0.94[ASN][1000 genomes]
rs61828370	0.95[ASN][1000 genomes]
rs6663482	0.96[ASN][1000 genomes]
rs7365663	0.86[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	nsv548339	chr1:179686244-179722827	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1009961	chr1:179714247-179790110	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179715200-179717600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:179717000-179719000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links