Variant report

Variant	rs4734519
Chromosome Location	chr8:92358729-92358730
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10088043	1.00[CHB][hapmap];0.88[AMR][1000 genomes]
rs10088955	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10092223	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10095567	0.96[YRI][hapmap]
rs10101012	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10109254	1.00[CHB][hapmap]
rs1125711	0.96[YRI][hapmap]
rs12334455	0.96[YRI][hapmap]
rs13248502	1.00[CHB][hapmap]
rs13248522	0.84[CEU][hapmap];1.00[CHB][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13254176	1.00[CHB][hapmap]
rs13263602	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13265284	1.00[CHB][hapmap]
rs13265723	1.00[CHB][hapmap]
rs13268588	1.00[CHB][hapmap]
rs13270617	1.00[JPT][hapmap]
rs13277179	1.00[CHB][hapmap]
rs1375246	1.00[CHB][hapmap]
rs1448677	0.90[AMR][1000 genomes]
rs17722765	1.00[CHB][hapmap]
rs2197810	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs2339303	1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4543502	1.00[CHB][hapmap]
rs4734520	1.00[JPT][hapmap]
rs6471276	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6471277	0.88[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6993516	1.00[CHB][hapmap]
rs6995526	1.00[CHB][hapmap]
rs7823182	1.00[CHB][hapmap]
rs7837310	1.00[CHB][hapmap]
rs921231	1.00[JPT][hapmap]
rs921232	1.00[CHB][hapmap]
rs921235	0.84[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028628	chr8:91680968-92418954	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539672	chr8:91680968-92418954	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv891190	chr8:92354921-92484872	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 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	chr8:92355800-92360000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:92357200-92361200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr8:92358200-92359000	Weak transcription	Brain Substantia Nigra	brain

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