Variant report

Variant	rs61990273
Chromosome Location	chr14:42012033-42012034
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10138559	0.84[EUR][1000 genomes]
rs10143349	0.87[EUR][1000 genomes]
rs10143445	0.87[EUR][1000 genomes]
rs10483526	0.82[ASN][1000 genomes]
rs1103437	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1103438	0.89[EUR][1000 genomes]
rs1111037	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11628212	0.87[EUR][1000 genomes]
rs12437380	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12589365	0.92[EUR][1000 genomes]
rs17781288	0.82[ASN][1000 genomes]
rs1953700	0.84[EUR][1000 genomes]
rs1953701	0.89[EUR][1000 genomes]
rs1956445	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1956450	0.82[ASN][1000 genomes]
rs1959411	0.89[EUR][1000 genomes]
rs1959412	0.84[EUR][1000 genomes]
rs1959413	0.84[EUR][1000 genomes]
rs2415678	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2415682	0.89[EUR][1000 genomes]
rs35583725	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3985189	0.85[EUR][1000 genomes]
rs3985190	0.92[EUR][1000 genomes]
rs4356390	0.82[ASN][1000 genomes]
rs55897228	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58114965	0.92[EUR][1000 genomes]
rs61990270	0.92[EUR][1000 genomes]
rs61990271	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990274	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990275	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990277	0.92[EUR][1000 genomes]
rs61990286	0.82[ASN][1000 genomes]
rs61990287	0.82[ASN][1000 genomes]
rs61990288	0.82[ASN][1000 genomes]
rs73309890	0.92[EUR][1000 genomes]
rs862475	0.92[EUR][1000 genomes]
rs862476	0.92[EUR][1000 genomes]
rs862478	0.89[EUR][1000 genomes]
rs862479	0.92[EUR][1000 genomes]
rs862480	0.89[EUR][1000 genomes]
rs862481	0.89[EUR][1000 genomes]
rs862482	0.89[EUR][1000 genomes]
rs9806026	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456224	chr14:41432350-42059281	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv564471	chr14:41432350-42059281	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1047300	chr14:41671653-42361098	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv1831164	chr14:41673017-42103168	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv533968	chr14:41882101-42327882	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv3439155	chr14:41984251-42014049	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv1042078	chr14:41993985-42120143	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' 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	chr14:42009600-42016400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:42011800-42013000	Genic enhancers	HUES6 Cell Line	embryonic stem cell
3	chr14:42012000-42013600	Genic enhancers	ES-I3 Cell Line	embryonic stem cell

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