Variant report

Variant	rs7735160
Chromosome Location	chr5:151985487-151985488
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11955130	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11960155	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17113408	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17113421	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17113482	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17113489	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17113492	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17113527	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17113590	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17113605	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34184277	0.89[EUR][1000 genomes]
rs4074300	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55970355	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57670604	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58616307	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58664268	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59054470	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61031397	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62395589	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62395590	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62395600	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62395602	0.80[EUR][1000 genomes]
rs62398711	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6869771	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6872346	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6875259	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6891765	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73801718	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7701379	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7702312	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7703966	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7703981	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7730407	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023676	chr5:151979253-152925064	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv537927	chr5:151979253-152925064	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr5:151975600-151985800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:151983000-151986000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:151983400-151988000	Weak transcription	Aorta	Aorta

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