Variant report

Variant	rs72676441
Chromosome Location	chr4:96271897-96271898
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:55)

rs_ID	r²[population]
rs10002089	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10023581	0.85[EUR][1000 genomes]
rs10024121	1.00[ASN][1000 genomes]
rs10029550	0.88[EUR][1000 genomes]
rs10516964	1.00[ASN][1000 genomes]
rs11097467	1.00[ASN][1000 genomes]
rs11728047	1.00[ASN][1000 genomes]
rs11735824	1.00[ASN][1000 genomes]
rs11943290	1.00[ASN][1000 genomes]
rs1384868	1.00[ASN][1000 genomes]
rs1586163	1.00[ASN][1000 genomes]
rs17023493	0.96[EUR][1000 genomes]
rs17023540	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17023543	1.00[ASN][1000 genomes]
rs17023545	1.00[ASN][1000 genomes]
rs17023617	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17023624	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17023627	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17369242	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2621442	1.00[ASN][1000 genomes]
rs2621443	1.00[ASN][1000 genomes]
rs2621446	1.00[ASN][1000 genomes]
rs2626054	1.00[ASN][1000 genomes]
rs2626055	1.00[ASN][1000 genomes]
rs2626056	1.00[ASN][1000 genomes]
rs28368523	1.00[ASN][1000 genomes]
rs28369639	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28417701	1.00[EUR][1000 genomes]
rs28475150	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28494154	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28526447	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28537146	1.00[ASN][1000 genomes]
rs28621043	1.00[ASN][1000 genomes]
rs28631733	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28689658	1.00[ASN][1000 genomes]
rs28692541	1.00[ASN][1000 genomes]
rs6532552	1.00[ASN][1000 genomes]
rs66536449	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66625786	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66969062	1.00[ASN][1000 genomes]
rs67577599	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67681548	0.89[EUR][1000 genomes]
rs67892114	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6816110	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6821360	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6848909	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6857369	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72676405	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72676414	0.89[EUR][1000 genomes]
rs72676415	0.89[EUR][1000 genomes]
rs72676421	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72676442	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7687905	1.00[ASN][1000 genomes]
rs9991852	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9999043	0.91[EUR][1000 genomes];1.00[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	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1001955	chr4:96216118-96445841	Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96239600-96284400	Weak transcription	Aorta	Aorta
2	chr4:96264200-96273000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:96264400-96283600	Weak transcription	Fetal Stomach	stomach

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