Variant report

Variant	rs891691
Chromosome Location	chr8:64336416-64336417
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10093298	0.97[EUR][1000 genomes]
rs10095044	0.97[EUR][1000 genomes]
rs10103710	0.83[EUR][1000 genomes]
rs10107912	0.83[EUR][1000 genomes]
rs10112423	0.95[EUR][1000 genomes]
rs1013259	0.97[EUR][1000 genomes]
rs10156375	0.80[EUR][1000 genomes]
rs1030584	0.82[EUR][1000 genomes]
rs1030585	0.82[EUR][1000 genomes]
rs1030586	0.82[EUR][1000 genomes]
rs10441558	0.94[EUR][1000 genomes]
rs10808732	0.98[EUR][1000 genomes]
rs10957282	0.83[EUR][1000 genomes]
rs10957283	0.83[EUR][1000 genomes]
rs10957285	0.97[EUR][1000 genomes]
rs11775060	0.98[EUR][1000 genomes]
rs11777936	0.98[EUR][1000 genomes]
rs11779425	0.94[EUR][1000 genomes]
rs11782289	0.95[EUR][1000 genomes]
rs11783042	0.94[EUR][1000 genomes]
rs11783055	0.94[EUR][1000 genomes]
rs11786252	0.94[EUR][1000 genomes]
rs12544518	0.85[EUR][1000 genomes]
rs12545091	0.94[EUR][1000 genomes]
rs12549069	0.97[EUR][1000 genomes]
rs12550189	0.92[EUR][1000 genomes]
rs13250116	0.97[EUR][1000 genomes]
rs13265562	0.97[EUR][1000 genomes]
rs13267865	0.97[EUR][1000 genomes]
rs13277482	0.83[EUR][1000 genomes]
rs1431591	0.98[EUR][1000 genomes]
rs1431594	0.84[ASN][1000 genomes]
rs16930415	0.82[EUR][1000 genomes]
rs2354894	0.98[EUR][1000 genomes]
rs28540225	0.82[EUR][1000 genomes]
rs28877014	0.97[EUR][1000 genomes]
rs35674021	0.82[EUR][1000 genomes]
rs4737646	0.97[EUR][1000 genomes]
rs4739089	0.96[EUR][1000 genomes]
rs4739090	0.96[EUR][1000 genomes]
rs4739091	0.98[EUR][1000 genomes]
rs6472103	0.85[EUR][1000 genomes]
rs6472104	0.85[EUR][1000 genomes]
rs6472106	0.80[EUR][1000 genomes]
rs6981013	0.81[EUR][1000 genomes]
rs6981563	0.80[EUR][1000 genomes]
rs6987680	0.97[EUR][1000 genomes]
rs6993493	0.81[EUR][1000 genomes]
rs6994236	0.97[EUR][1000 genomes]
rs6997547	0.94[EUR][1000 genomes]
rs7006972	0.96[EUR][1000 genomes]
rs7462242	0.98[EUR][1000 genomes]
rs7825481	0.98[EUR][1000 genomes]
rs7834350	0.98[EUR][1000 genomes]
rs7840470	0.85[EUR][1000 genomes]
rs7841852	0.94[EUR][1000 genomes]
rs9298075	0.83[EUR][1000 genomes]
rs9298077	0.95[EUR][1000 genomes]
rs974555	0.83[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890967	chr8:64107847-64454446	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr8:64322000-64337000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:64332200-64340200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr8:64332600-64340200	Weak transcription	HSMM	muscle

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