Variant report

Variant	rs2924719
Chromosome Location	chr8:4839733-4839734
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10088688	0.89[CEU][hapmap];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10094549	0.81[CEU][hapmap]
rs10101412	0.95[CEU][hapmap];0.81[CHB][hapmap];0.81[JPT][hapmap]
rs10103830	0.86[CHB][hapmap]
rs1011587	0.89[CEU][hapmap]
rs10503294	0.81[CEU][hapmap]
rs10503296	0.84[CEU][hapmap]
rs11778422	0.80[EUR][1000 genomes]
rs11781399	0.90[CHB][hapmap]
rs12114470	0.81[CEU][hapmap]
rs12155630	0.84[CEU][hapmap]
rs12674915	0.80[CEU][hapmap]
rs13248218	0.80[CEU][hapmap]
rs13254311	0.81[CEU][hapmap]
rs13264559	0.95[CEU][hapmap]
rs13273154	0.80[CEU][hapmap]
rs13439499	0.80[CHB][hapmap]
rs17071958	0.86[CHB][hapmap]
rs17071968	0.85[CHB][hapmap]
rs2924720	0.95[CEU][hapmap];0.82[CHB][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2924721	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2924723	0.90[CEU][hapmap];0.81[JPT][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2924724	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs2977726	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2977727	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2977732	0.89[CEU][hapmap]
rs2977733	0.85[CEU][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs4272399	0.81[EUR][1000 genomes]
rs4278171	1.00[CEU][hapmap]
rs4295679	0.81[CEU][hapmap]
rs4329292	0.90[CEU][hapmap]
rs4360313	0.81[CEU][hapmap]
rs4385481	0.81[CEU][hapmap]
rs4436145	0.84[ASN][1000 genomes]
rs4477045	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4495447	0.90[CEU][hapmap];0.80[EUR][1000 genomes]
rs4517142	0.90[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4517143	0.95[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4521778	0.81[ASN][1000 genomes]
rs4593564	0.85[CHB][hapmap]
rs4593565	0.90[CEU][hapmap]
rs4614018	0.90[CEU][hapmap]
rs4623447	0.80[CEU][hapmap]
rs4875426	0.95[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4875427	0.95[CEU][hapmap];0.82[CHB][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6558951	0.95[CEU][hapmap]
rs7007684	0.86[CHB][hapmap]
rs7832116	0.80[CHB][hapmap]
rs7833750	0.90[CHB][hapmap]
rs9657374	0.90[CHB][hapmap];0.87[ASN][1000 genomes]
rs9657406	0.86[CHB][hapmap]
rs9657407	0.85[CHB][hapmap]

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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4832000-4848200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:4835200-4847200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr8:4835600-4848200	Weak transcription	Brain Angular Gyrus	brain
4	chr8:4838800-4840200	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chr8:4839600-4840000	Enhancers	Fetal Heart	heart

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