Variant report

Variant	rs2018136
Chromosome Location	chr3:28473575-28473576
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11707705	0.80[ASN][1000 genomes]
rs11926399	0.80[ASN][1000 genomes]
rs13065010	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13069839	0.83[ASN][1000 genomes]
rs13070434	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13074633	0.80[ASN][1000 genomes]
rs13075840	0.80[ASN][1000 genomes]
rs13080155	0.80[ASN][1000 genomes]
rs13085075	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13087143	0.80[ASN][1000 genomes]
rs13087774	0.80[ASN][1000 genomes]
rs13088574	0.80[ASN][1000 genomes]
rs13095675	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13101128	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1457910	0.80[ASN][1000 genomes]
rs1585211	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17696459	0.80[ASN][1000 genomes]
rs17696561	0.80[ASN][1000 genomes]
rs1870259	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1975828	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1975829	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2168799	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4327342	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4680750	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4680909	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4680910	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4680913	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62250271	0.80[ASN][1000 genomes]
rs62250272	0.80[ASN][1000 genomes]
rs6762636	0.87[EUR][1000 genomes]
rs6763313	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6771057	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6777813	0.83[AFR][1000 genomes]
rs6803692	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7638450	0.80[ASN][1000 genomes]
rs7639750	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7641491	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7649498	0.81[AFR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7650742	0.83[EUR][1000 genomes]
rs7651883	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9843464	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3328565	chr3:27991169-28915035	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv876649	chr3:28126595-28718454	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv876650	chr3:28427029-28613602	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1015015	chr3:28461972-28728494	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv916364	chr3:28468275-29146280	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv590010	chr3:28469830-28727214	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:28471800-28479600	Weak transcription	Left Ventricle	heart
2	chr3:28473200-28492400	Weak transcription	Gastric	stomach

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