Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10088688	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10101412	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11778422	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2924719	0.81[ASN][1000 genomes]
rs2924720	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2924721	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2924723	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2924724	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2977694	0.81[AMR][1000 genomes]
rs2977726	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2977727	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2977732	0.87[AMR][1000 genomes]
rs2977733	0.82[AMR][1000 genomes]
rs4272399	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4436145	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4477045	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4495447	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4517142	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4517143	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4614018	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4875426	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4875427	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[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	nsv609876	chr8:4494811-5092970	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1029480	chr8:4497596-5081032	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv498130	chr8:4532988-5176376	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1031026	chr8:4771072-5054326	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1031402	chr8:4827087-4842934	Strong transcription Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4831400-4838800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:4832000-4848200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:4835200-4847200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr8:4835600-4848200	Weak transcription	Brain Angular Gyrus	brain

Quick Search: