Variant report

Variant	rs2876376
Chromosome Location	chr20:14262543-14262544
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs17263597	0.94[ASN][1000 genomes]
rs2038505	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs204605	0.81[ASN][1000 genomes]
rs204606	0.81[ASN][1000 genomes]
rs204633	0.82[ASN][1000 genomes]
rs2208453	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2208455	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2256118	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2327840	0.91[ASN][1000 genomes]
rs2327841	0.95[ASN][1000 genomes]
rs2327842	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2327843	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2327845	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2423778	0.95[ASN][1000 genomes]
rs2423779	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4814293	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58243986	0.92[ASN][1000 genomes]
rs58623651	0.94[ASN][1000 genomes]
rs58694064	0.95[ASN][1000 genomes]
rs6033927	0.93[ASN][1000 genomes]
rs6033931	0.96[ASN][1000 genomes]
rs6033932	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6033933	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6033941	0.83[ASN][1000 genomes]
rs6042648	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6042652	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6042653	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6042669	0.80[ASN][1000 genomes]
rs6079380	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6135113	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs718705	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7263144	0.93[ASN][1000 genomes]
rs7271710	0.95[ASN][1000 genomes]
rs8116353	0.91[ASN][1000 genomes]
rs8123052	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs994567	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066810	chr20:13451869-14432454	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv531479	chr20:13632491-14434432	Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1057486	chr20:14077828-14469129	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv532514	chr20:14097780-14288315	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1066235	chr20:14173771-14389050	Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv458872	chr20:14189779-14317390	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv470540	chr20:14189779-14317390	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv585439	chr20:14189779-14317390	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1066105	chr20:14201909-14272115	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1055499	chr20:14224873-14848061	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers 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:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14259000-14263400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr20:14260000-14263200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr20:14261400-14263000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr20:14261400-14265000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr20:14261600-14263000	Weak transcription	HMEC	breast
6	chr20:14261600-14263000	Weak transcription	NHEK	skin

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