Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10009979	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10011270	0.83[ASN][1000 genomes]
rs10012425	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10021032	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10084895	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10084947	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11097386	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12505322	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13110968	0.84[ASN][1000 genomes]
rs13117830	0.88[ASN][1000 genomes]
rs1371359	0.80[AMR][1000 genomes]
rs1439548	0.80[AMR][1000 genomes]
rs17296189	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28511876	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28699218	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs36108466	0.82[ASN][1000 genomes]
rs4619859	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4692991	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4693343	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs66548721	0.83[ASN][1000 genomes]
rs6837139	0.82[EUR][1000 genomes]
rs6848798	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs732020	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs893708	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs963026	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9993013	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9998217	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008055	chr4:94169131-95030074	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv931979	chr4:94289958-95121723	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv821636	chr4:94439636-95116590	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1013018	chr4:94526959-94735442	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:94670600-94684000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:94671200-94680000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:94676200-94676800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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