Variant report

Variant	rs2105058
Chromosome Location	chr14:56304304-56304305
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	chr14:56302735..56305640-chr14:56310752..56313567,2	MCF-7	breast:
2	chr14:56300351..56302227-chr14:56304134..56305783,2	MCF-7	breast:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10134507	0.83[EUR][1000 genomes]
rs11620875	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11621835	0.94[EUR][1000 genomes]
rs11622627	0.84[EUR][1000 genomes]
rs11622641	0.84[EUR][1000 genomes]
rs11622710	0.83[EUR][1000 genomes]
rs11624167	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11624516	0.87[EUR][1000 genomes]
rs11625571	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11625869	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11626057	0.94[EUR][1000 genomes]
rs11627629	0.84[EUR][1000 genomes]
rs11628040	0.84[EUR][1000 genomes]
rs12883012	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12890121	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12894971	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17253841	0.84[EUR][1000 genomes]
rs17832467	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1999705	0.86[EUR][1000 genomes]
rs1999706	0.86[EUR][1000 genomes]
rs2152287	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2342594	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2342595	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28490128	0.86[ASN][1000 genomes]
rs34096981	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34186256	0.81[EUR][1000 genomes]
rs34421003	0.86[EUR][1000 genomes]
rs34535564	0.81[EUR][1000 genomes]
rs34540577	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34663121	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35094937	0.81[EUR][1000 genomes]
rs35290945	0.94[EUR][1000 genomes]
rs35527253	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35559254	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35813917	0.81[EUR][1000 genomes]
rs36096896	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs36112734	0.81[EUR][1000 genomes]
rs36120082	0.81[EUR][1000 genomes]
rs36149160	0.85[EUR][1000 genomes]
rs36188950	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4601950	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55788205	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55837858	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57658601	0.86[EUR][1000 genomes]
rs61975563	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61975579	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61977780	0.84[EUR][1000 genomes]
rs61977781	0.84[EUR][1000 genomes]
rs61977782	0.84[EUR][1000 genomes]
rs61977785	0.85[EUR][1000 genomes]
rs71412700	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs999817	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[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	nsv901966	chr14:56160904-56436203	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv901977	chr14:56213392-56492996	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56304000-56304600	Enhancers	HepG2	liver
2	chr14:56304200-56304400	Enhancers	Fetal Intestine Small	intestine
3	chr14:56304200-56304600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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