Variant report

Variant	rs62267777
Chromosome Location	chr3:75062144-75062145
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs11709921	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11920209	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12054293	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12054432	0.80[ASN][1000 genomes]
rs12171270	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12486094	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12629483	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12632116	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12632660	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4073454	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4076158	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4298078	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4340743	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4346587	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4349537	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4356853	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4368539	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4449358	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4467494	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4544657	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4589972	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4607148	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4635750	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs5009222	0.80[ASN][1000 genomes]
rs62258901	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62266825	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6549681	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6549685	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6761963	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6786444	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6796018	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6801622	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7616253	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7652902	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9310311	0.84[EUR][1000 genomes]
rs9815881	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9825398	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9829306	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9833132	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9842069	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9850353	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9863946	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9868696	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9869833	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9877977	0.84[EUR][1000 genomes]
rs9881282	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529994	chr3:74720752-75471887	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
2	nsv916594	chr3:74943399-75540161	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	esv1851336	chr3:74970564-75280989	ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv876959	chr3:74989983-75076440	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1005139	chr3:75027834-75168557	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv534344	chr3:75028665-75164716	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75061000-75063600	Enhancers	Brain Germinal Matrix	brain
2	chr3:75061200-75063000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:75061400-75064000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr3:75061600-75062800	Enhancers	Fetal Heart	heart
5	chr3:75061600-75063400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr3:75061800-75063200	Weak transcription	Fetal Brain Male	brain
7	chr3:75061800-75064200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr3:75062000-75062800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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