Variant report

Variant	rs4650425
Chromosome Location	chr1:80117634-80117635
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10493651	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11162775	0.86[EUR][1000 genomes]
rs11162786	0.85[AMR][1000 genomes]
rs11799706	0.86[EUR][1000 genomes]
rs12076080	0.85[AMR][1000 genomes]
rs12118867	0.81[AMR][1000 genomes]
rs12119749	0.84[EUR][1000 genomes]
rs12120408	0.85[EUR][1000 genomes]
rs12122884	0.88[AMR][1000 genomes]
rs12128027	0.87[EUR][1000 genomes]
rs12133798	0.87[AMR][1000 genomes]
rs12144677	0.84[AMR][1000 genomes]
rs12144807	0.84[AMR][1000 genomes]
rs12724652	0.85[AMR][1000 genomes]
rs12726232	0.86[AMR][1000 genomes]
rs12727301	0.85[EUR][1000 genomes]
rs12728973	0.86[EUR][1000 genomes]
rs12737717	0.86[AMR][1000 genomes]
rs12744936	0.86[EUR][1000 genomes]
rs12749085	0.88[EUR][1000 genomes]
rs12752633	0.87[AMR][1000 genomes]
rs12755043	0.86[EUR][1000 genomes]
rs12759746	0.89[AMR][1000 genomes]
rs12759996	0.82[EUR][1000 genomes]
rs4650426	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5010880	0.87[AMR][1000 genomes]
rs60192560	0.86[EUR][1000 genomes]
rs6698618	0.85[EUR][1000 genomes]
rs6700113	0.85[EUR][1000 genomes]
rs71504618	0.80[EUR][1000 genomes]
rs726964	0.85[EUR][1000 genomes]
rs7533906	0.83[EUR][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	nsv1012296	chr1:79945395-80300216	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers 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
2	nsv546637	chr1:79984748-80159969	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1012286	chr1:80057078-81005153	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv535018	chr1:80057078-81005153	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv1000792	chr1:80076146-81015283	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr1:80113000-80118200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:80113200-80123200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:80116400-80119200	Enhancers	Fetal Heart	heart

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