Variant report

Variant	rs61990335
Chromosome Location	chr14:42177797-42177798
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10131184	0.81[ASN][1000 genomes]
rs11628299	0.81[ASN][1000 genomes]
rs1597049	0.94[ASN][1000 genomes]
rs17112192	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17181601	0.94[ASN][1000 genomes]
rs17181608	0.94[ASN][1000 genomes]
rs17181615	0.94[ASN][1000 genomes]
rs17181622	0.94[ASN][1000 genomes]
rs17181636	0.94[ASN][1000 genomes]
rs17781361	0.94[ASN][1000 genomes]
rs4584739	0.94[ASN][1000 genomes]
rs4586337	0.94[ASN][1000 genomes]
rs4603462	0.94[ASN][1000 genomes]
rs4624078	0.94[ASN][1000 genomes]
rs59082466	0.94[ASN][1000 genomes]
rs61990287	0.84[AMR][1000 genomes]
rs61990338	0.82[ASN][1000 genomes]
rs61990339	0.94[ASN][1000 genomes]
rs61990342	0.82[ASN][1000 genomes]
rs61990343	0.94[ASN][1000 genomes]
rs61990345	0.94[ASN][1000 genomes]
rs61990347	0.94[ASN][1000 genomes]
rs61990349	0.94[ASN][1000 genomes]
rs61992404	0.94[ASN][1000 genomes]
rs61992433	0.81[ASN][1000 genomes]
rs7143254	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72686527	0.94[ASN][1000 genomes]
rs72686528	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	esv2758353	chr14:42045873-42259511	Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv2759983	chr14:42045873-42259511	ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv901738	chr14:42145461-42302552	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42177400-42178000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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