Variant report

Variant	rs35438476
Chromosome Location	chr20:14356704-14356705
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs13036915	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13037096	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13038084	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13039855	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13039862	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13040337	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13040558	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13040987	0.81[EUR][1000 genomes]
rs13042179	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13042866	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13044911	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17226957	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17226971	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17226999	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17812658	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1998236	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2210655	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34021592	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34085437	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34094793	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34522477	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34538736	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34880844	0.81[AMR][1000 genomes]
rs34896694	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34985688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35346025	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35445955	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35505382	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35554517	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35577212	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35631624	0.81[EUR][1000 genomes]
rs35733982	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35943017	0.81[EUR][1000 genomes]
rs35989081	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36062805	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs41328645	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4630827	0.81[EUR][1000 genomes]
rs4814301	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62204373	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62204396	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62204398	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62204402	0.81[EUR][1000 genomes]
rs62204403	0.81[EUR][1000 genomes]
rs62207626	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62207627	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62207628	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74179739	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs74179740	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs915074	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs915075	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs963329	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	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
5	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
6	nsv1061705	chr20:14330029-14430604	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1062079	chr20:14334350-14429820	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1063787	chr20:14341199-14408090	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv585440	chr20:14352394-14457834	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14351600-14359000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr20:14353200-14357000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr20:14353200-14357200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr20:14353400-14359400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr20:14354000-14357200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr20:14354800-14357000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr20:14356000-14357200	Enhancers	Fetal Intestine Large	intestine
8	chr20:14356000-14357200	Enhancers	Fetal Intestine Small	intestine
9	chr20:14356200-14356800	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr20:14356600-14356800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr20:14356600-14365200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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