Variant report

Variant	rs2866286
Chromosome Location	chr4:78305119-78305120
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10000203	0.96[ASN][1000 genomes]
rs10021013	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10022216	0.94[ASN][1000 genomes]
rs10024634	0.94[ASN][1000 genomes]
rs10025816	0.96[ASN][1000 genomes]
rs10031995	0.96[ASN][1000 genomes]
rs10034168	0.96[ASN][1000 genomes]
rs12502190	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17002573	0.92[ASN][1000 genomes]
rs17002575	0.92[ASN][1000 genomes]
rs17002578	0.92[ASN][1000 genomes]
rs17002614	0.85[EUR][1000 genomes]
rs17002672	0.87[EUR][1000 genomes]
rs1962027	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28408985	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28470829	0.97[ASN][1000 genomes]
rs28509428	0.97[ASN][1000 genomes]
rs28510834	0.97[ASN][1000 genomes]
rs28558753	0.97[ASN][1000 genomes]
rs28640182	0.96[ASN][1000 genomes]
rs28659994	0.92[EUR][1000 genomes]
rs2866283	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28715173	0.85[EUR][1000 genomes]
rs28771770	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28821633	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28822468	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28844066	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28886989	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3886412	0.96[ASN][1000 genomes]
rs4146559	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4426805	0.96[ASN][1000 genomes]
rs4447887	0.97[ASN][1000 genomes]
rs4586976	0.92[EUR][1000 genomes]
rs4643843	0.96[ASN][1000 genomes]
rs4859826	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56704522	0.92[ASN][1000 genomes]
rs57255185	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57851138	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57854205	0.92[ASN][1000 genomes]
rs58210020	0.97[ASN][1000 genomes]
rs58493318	0.97[ASN][1000 genomes]
rs58763343	0.96[ASN][1000 genomes]
rs59017002	0.97[ASN][1000 genomes]
rs59225688	0.97[ASN][1000 genomes]
rs59548585	0.97[ASN][1000 genomes]
rs59817506	0.97[ASN][1000 genomes]
rs60084947	0.97[ASN][1000 genomes]
rs60847680	0.97[ASN][1000 genomes]
rs60994753	0.96[ASN][1000 genomes]
rs61041046	0.97[ASN][1000 genomes]
rs61482056	0.97[ASN][1000 genomes]
rs61559911	0.97[ASN][1000 genomes]
rs6819777	0.91[ASN][1000 genomes]
rs6832224	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6850445	0.80[EUR][1000 genomes]
rs72859841	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72859843	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72859844	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7666881	0.92[ASN][1000 genomes]
rs9307270	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006017	chr4:78139780-78312974	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1010450	chr4:78182037-78317840	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1004824	chr4:78188691-78312974	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv1845782	chr4:78237955-78321598	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv829974	chr4:78240718-78415642	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv3442840	chr4:78277532-78309591	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv594698	chr4:78291876-78334483	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv967998	chr4:78301212-78311035	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78298400-78306800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr4:78300600-78306200	Weak transcription	Fetal Intestine Small	intestine

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